Item | Value |
---|---|
geneid | 9790 |
ensemblid | ENSG00000165733.8 |
hgncid | 23505 |
symbol | BMS1 |
name | BMS1 ribosome biogenesis factor |
refseq_nuc | NM_014753.4 |
refseq_prot | NP_055568.3 |
ensembl_nuc | ENST00000374518.6 |
ensembl_prot | ENSP00000363642.4 |
mane_status | MANE Select |
chr | chr10 |
start | 42782795 |
end | 42834937 |
strand | + |
ver | v1.2 |
region | chr10:42782795-42834937 |
region5000 | chr10:42777795-42839937 |
regionname0 | BMS1_chr10_42782795_42834937 |
regionname5000 | BMS1_chr10_42777795_42839937 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1282 | 155 | 56 | 40 | 29 | 10 | 19 | 19 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0002 | 0/1 | 1282 | 82 | 17 | 22 | 35 | 1 | 6 | 29 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0003 | 0/0 | 1282 | 70 | 3 | 8 | 40 | 5 | 14 | 28 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0004 | 0/0 | 1282 | 31 | 0 | 0 | 31 | 0 | 0 | 27 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0005 | 0/0 | 1282 | 19 | 0 | 1 | 18 | 0 | 0 | 14 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0006 | 0/0 | 1282 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0007 | 0/0 | 1282 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0008 | 0/0 | 1282 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0009 | 0/0 | 1282 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0010 | 0/0 | 1282 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0011 | 0/0 | 1282 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0012 | 0/0 | 1282 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0013 | 0/0 | 1282 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0014 | 0/0 | 1282 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0015 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0016 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0017 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0018 | 0/0 | 1282 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0019 | 0/0 | 1282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0020 | 0/0 | 1282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0021 | 0/0 | 1282 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0022 | 0/0 | 1282 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0023 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0024 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0025 | 0/0 | 1282 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0026 | 0/0 | 1282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
a0027 | 0/0 | 1282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | MEAKD others(1277): Show |
chr10 | 42777795 | 42839937 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003 | 1/0 | 3846 | 58 | 12 | 14 | 15 | 7 | 9 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0004 | 0/0 | 3846 | 48 | 23 | 15 | 3 | 0 | 7 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0005 | 0/0 | 3846 | 34 | 16 | 5 | 11 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0008 | 0/0 | 3846 | 11 | 3 | 4 | 0 | 3 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0013 | 0/0 | 3846 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0026 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0001c0030 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0002c0001 | 0/1 | 3846 | 81 | 17 | 21 | 35 | 1 | 6 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0002c0028 | 0/0 | 3846 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0003c0002 | 0/0 | 3846 | 67 | 2 | 8 | 39 | 4 | 14 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0003c0025 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0003c0027 | 0/0 | 3846 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0003c0031 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0004c0006 | 0/0 | 3846 | 28 | 0 | 0 | 28 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0004c0010 | 0/0 | 3846 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0005c0007 | 0/0 | 3846 | 19 | 0 | 1 | 18 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0006c0009 | 0/0 | 3846 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0007c0014 | 0/0 | 3846 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0008c0016 | 0/0 | 3846 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0009c0011 | 0/0 | 3846 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0010c0012 | 0/0 | 3846 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0011c0017 | 0/0 | 3846 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0012c0015 | 0/0 | 3846 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0013c0018 | 0/0 | 3846 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0014c0019 | 0/0 | 3846 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0015c0035 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0016c0032 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0017c0029 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0018c0021 | 0/0 | 3846 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0019c0034 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0020c0037 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0021c0022 | 0/0 | 3846 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0022c0033 | 0/0 | 3846 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0023c0024 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0024c0023 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0025c0036 | 0/0 | 3846 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0026c0020 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 | ||
a0027c0038 | 0/0 | 3846 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | ATGGA others(3841): Show |
chr10 | 42777795 | 42839937 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0001 | 0/0 | 7758 | 41 | 11 | 9 | 13 | 4 | 4 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0006 | 1/0 | 7759 | 7 | 1 | 3 | 0 | 1 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7754): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0009 | 0/0 | 7758 | 4 | 0 | 2 | 0 | 2 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0010 | 0/0 | 7758 | 3 | 0 | 0 | 0 | 0 | 3 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0020 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0021 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0003t0023 | 0/0 | 7758 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0003 | 0/0 | 7748 | 42 | 17 | 15 | 3 | 0 | 7 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7743): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0011 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0018 | 0/0 | 7758 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0028 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7754): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0029 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0001c0004t0033 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0005t0004 | 0/0 | 7752 | 32 | 15 | 5 | 10 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7747): Show |
chr10 | 42777795 | 42839937 |
a0001c0005t0025 | 0/0 | 7752 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7747): Show |
chr10 | 42777795 | 42839937 |
a0001c0005t0026 | 0/0 | 7752 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7747): Show |
chr10 | 42777795 | 42839937 |
a0001c0008t0007 | 0/0 | 7753 | 6 | 1 | 2 | 0 | 3 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0008t0008 | 0/0 | 7753 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0008t0015 | 0/0 | 7753 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0008t0019 | 0/0 | 7753 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0013t0008 | 0/0 | 7753 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0026t0013 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0001c0030t0032 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0002c0001t0001 | 0/1 | 7758 | 76 | 17 | 18 | 34 | 0 | 6 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0002c0001t0016 | 0/0 | 7758 | 2 | 0 | 1 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0002c0001t0017 | 0/0 | 7758 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0002c0001t0022 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0002c0028t0001 | 0/0 | 7758 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0002t0002 | 0/0 | 7758 | 62 | 2 | 8 | 35 | 4 | 13 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0002t0012 | 0/0 | 7758 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0002t0027 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0002t0030 | 0/0 | 7758 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0025t0002 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0027t0002 | 0/0 | 7758 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0003c0031t0002 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0004c0006t0005 | 0/0 | 7753 | 27 | 0 | 0 | 27 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0004c0006t0031 | 0/0 | 7754 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7749): Show |
chr10 | 42777795 | 42839937 |
a0004c0010t0005 | 0/0 | 7753 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0005c0007t0001 | 0/0 | 7758 | 18 | 0 | 1 | 17 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0005c0007t0024 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0006c0009t0002 | 0/0 | 7758 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0007c0014t0011 | 0/0 | 7753 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0008c0016t0013 | 0/0 | 7753 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0009c0011t0002 | 0/0 | 7758 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0010c0012t0014 | 0/0 | 7758 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0011c0017t0001 | 0/0 | 7758 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0012c0015t0003 | 0/0 | 7748 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7743): Show |
chr10 | 42777795 | 42839937 |
a0013c0018t0004 | 0/0 | 7752 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7747): Show |
chr10 | 42777795 | 42839937 |
a0014c0019t0003 | 0/0 | 7748 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7743): Show |
chr10 | 42777795 | 42839937 |
a0015c0035t0001 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0016c0032t0001 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0017c0029t0005 | 0/0 | 7753 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0018c0021t0005 | 0/0 | 7753 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0019c0034t0001 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0020c0037t0001 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0021c0022t0002 | 0/0 | 7758 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0022c0033t0001 | 0/0 | 7758 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0023c0024t0005 | 0/0 | 7753 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0024c0023t0005 | 0/0 | 7753 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0025c0036t0001 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
a0026c0020t0008 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7748): Show |
chr10 | 42777795 | 42839937 |
a0027c0038t0001 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | GTCCA others(7753): Show |
chr10 | 42777795 | 42839937 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0006 | 0/0 | 6 | 1 | 0 | 0 | 4 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0006g0020 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0006g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0009g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0009g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0010g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0010g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0021g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0003t0023g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0028g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0029g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0004t0033g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0025g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0005t0026g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0007g0014 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0007g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0008g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0015g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0015g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0008t0019g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0013t0008g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0026t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0001c0030t0032g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0005 | 0/0 | 8 | 0 | 4 | 2 | 0 | 2 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0016g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0016g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0017g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0017g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0001t0022g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0002c0028t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0001 | 0/0 | 23 | 0 | 3 | 12 | 3 | 5 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0012g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0027g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0002t0030g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0025t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0027t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0003c0031t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0006t0031g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0010t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0004c0010t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0005c0007t0024g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0006c0009t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0006c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0006c0009t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0007c0014t0011g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0007c0014t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0008c0016t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0008c0016t0013g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0009c0011t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0009c0011t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0010c0012t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0010c0012t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0011c0017t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0011c0017t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0012c0015t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0012c0015t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0013c0018t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0013c0018t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0014c0019t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0015c0035t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0016c0032t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0017c0029t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0018c0021t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0019c0034t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0020c0037t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0021c0022t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0022c0033t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0023c0024t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0024c0023t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0025c0036t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0026c0020t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
a0027c0038t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0008 | t0007 | g0014 | EUR | GBR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | GBR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00140 | hp1 | a0001 | c0008 | t0007 | g0154 | EUR | GBR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00140 | hp2 | a0001 | c0003 | t0006 | g0030 | EUR | GBR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00280 | hp1 | a0003 | c0002 | t0002 | g0001 | EUR | FIN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | FIN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00323 | hp1 | a0003 | c0002 | t0002 | g0001 | EUR | FIN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | FIN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00408 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0229 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0254 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00544 | hp1 | a0003 | c0002 | t0002 | g0080 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00544 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00558 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00558 | hp2 | a0003 | c0002 | t0002 | g0115 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0209 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00597 | hp2 | a0003 | c0002 | t0002 | g0088 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00609 | hp1 | a0003 | c0002 | t0002 | g0081 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00609 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00621 | hp1 | a0003 | c0002 | t0002 | g0089 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00621 | hp2 | a0002 | c0001 | t0022 | g0009 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00639 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00642 | hp2 | a0003 | c0002 | t0002 | g0104 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00673 | hp2 | a0005 | c0007 | t0001 | g0029 | EAS | CHS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00733 | hp1 | a0002 | c0001 | t0001 | g0220 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00733 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00735 | hp1 | a0001 | c0008 | t0015 | g0158 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0247 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG00741 | hp2 | a0003 | c0002 | t0002 | g0022 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01069 | hp2 | a0001 | c0013 | t0008 | g0028 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01070 | hp1 | a0001 | c0004 | t0003 | g0061 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01070 | hp2 | a0003 | c0002 | t0002 | g0023 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01071 | hp1 | a0003 | c0002 | t0002 | g0023 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01071 | hp2 | a0001 | c0013 | t0008 | g0028 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01081 | hp1 | a0001 | c0004 | t0003 | g0007 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01081 | hp2 | a0001 | c0003 | t0006 | g0020 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01099 | hp1 | a0001 | c0004 | t0003 | g0072 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01099 | hp2 | a0002 | c0001 | t0016 | g0005 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01106 | hp1 | a0001 | c0004 | t0003 | g0150 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01106 | hp2 | a0003 | c0002 | t0002 | g0097 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01109 | hp1 | a0007 | c0014 | t0011 | g0040 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01109 | hp2 | a0001 | c0003 | t0006 | g0203 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01167 | hp1 | a0001 | c0004 | t0003 | g0149 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01167 | hp2 | a0002 | c0001 | t0017 | g0243 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01168 | hp1 | a0001 | c0003 | t0009 | g0035 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01168 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01169 | hp1 | a0001 | c0003 | t0009 | g0035 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01169 | hp2 | a0002 | c0001 | t0017 | g0242 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0037 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01192 | hp2 | a0001 | c0004 | t0003 | g0021 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0240 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01243 | hp2 | a0001 | c0008 | t0008 | g0027 | AMR | PUR | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0235 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01256 | hp1 | a0014 | c0019 | t0003 | g0007 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0227 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01257 | hp2 | a0001 | c0004 | t0003 | g0007 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01258 | hp1 | a0001 | c0004 | t0003 | g0007 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0205 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01261 | hp2 | a0001 | c0004 | t0003 | g0056 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01358 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0214 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01433 | hp1 | a0001 | c0003 | t0006 | g0030 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01496 | hp1 | a0001 | c0004 | t0003 | g0007 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01516 | hp1 | a0001 | c0003 | t0009 | g0034 | EUR | IBS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01516 | hp2 | a0001 | c0008 | t0007 | g0157 | EUR | IBS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01517 | hp1 | a0003 | c0002 | t0002 | g0086 | EUR | IBS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01517 | hp2 | a0001 | c0003 | t0009 | g0034 | EUR | IBS | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01884 | hp1 | a0001 | c0003 | t0006 | g0201 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01884 | hp2 | a0007 | c0014 | t0011 | g0041 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0148 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01891 | hp2 | a0001 | c0004 | t0029 | g0078 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01928 | hp1 | a0001 | c0004 | t0003 | g0065 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01928 | hp2 | a0001 | c0005 | t0004 | g0013 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01934 | hp1 | a0001 | c0004 | t0003 | g0058 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01934 | hp2 | a0001 | c0008 | t0007 | g0014 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01943 | hp2 | a0001 | c0005 | t0004 | g0127 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01952 | hp1 | a0002 | c0001 | t0001 | g0215 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01975 | hp1 | a0001 | c0004 | t0003 | g0070 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01978 | hp1 | a0008 | c0016 | t0013 | g0047 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01978 | hp2 | a0001 | c0005 | t0004 | g0128 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02027 | hp1 | a0003 | c0002 | t0002 | g0103 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02027 | hp2 | a0003 | c0002 | t0002 | g0085 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02040 | hp1 | a0004 | c0006 | t0005 | g0175 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02040 | hp2 | a0005 | c0007 | t0001 | g0002 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0238 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0071 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02056 | hp2 | a0009 | c0011 | t0002 | g0113 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02074 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02074 | hp2 | a0015 | c0035 | t0001 | g0225 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02080 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02080 | hp2 | a0016 | c0032 | t0001 | g0120 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02083 | hp1 | a0001 | c0005 | t0004 | g0131 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02083 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02129 | hp2 | a0006 | c0009 | t0002 | g0084 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02132 | hp1 | a0001 | c0005 | t0004 | g0130 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02135 | hp1 | a0001 | c0004 | t0003 | g0057 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02135 | hp2 | a0001 | c0005 | t0004 | g0121 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02145 | hp1 | a0001 | c0005 | t0004 | g0134 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0259 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02148 | hp1 | a0001 | c0005 | t0004 | g0126 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0185 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02155 | hp1 | a0003 | c0002 | t0012 | g0001 | EAS | CDX | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02155 | hp2 | a0001 | c0005 | t0004 | g0012 | EAS | CDX | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02165 | hp1 | a0005 | c0007 | t0001 | g0191 | EAS | CDX | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02165 | hp2 | a0003 | c0002 | t0002 | g0079 | EAS | CDX | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02257 | hp1 | a0001 | c0004 | t0003 | g0066 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0037 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0241 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02258 | hp2 | a0002 | c0001 | t0001 | g0182 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02273 | hp1 | a0001 | c0004 | t0003 | g0059 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02273 | hp2 | a0005 | c0007 | t0001 | g0194 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02280 | hp1 | a0002 | c0001 | t0001 | g0009 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02280 | hp2 | a0001 | c0008 | t0015 | g0159 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02293 | hp1 | a0002 | c0001 | t0001 | g0206 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02293 | hp2 | a0001 | c0005 | t0004 | g0013 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02300 | hp1 | a0001 | c0008 | t0007 | g0155 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02300 | hp2 | a0002 | c0028 | t0001 | g0217 | AMR | PEL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02523 | hp2 | a0017 | c0029 | t0005 | g0003 | EAS | KHV | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02572 | hp1 | a0010 | c0012 | t0014 | g0261 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02602 | hp1 | a0001 | c0003 | t0010 | g0002 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02602 | hp2 | a0018 | c0021 | t0005 | g0177 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02615 | hp1 | a0001 | c0004 | t0003 | g0074 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02615 | hp2 | a0008 | c0016 | t0013 | g0046 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02622 | hp1 | a0001 | c0030 | t0032 | g0043 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02630 | hp1 | a0011 | c0017 | t0001 | g0231 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0245 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0135 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0248 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02683 | hp2 | a0001 | c0004 | t0003 | g0063 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0032 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02698 | hp2 | a0003 | c0002 | t0002 | g0114 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02717 | hp1 | a0001 | c0004 | t0003 | g0026 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02723 | hp1 | a0003 | c0002 | t0002 | g0110 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02723 | hp2 | a0001 | c0005 | t0004 | g0140 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02735 | hp1 | a0001 | c0004 | t0003 | g0055 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02735 | hp2 | a0001 | c0008 | t0019 | g0156 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02738 | hp1 | a0001 | c0003 | t0006 | g0020 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02738 | hp2 | a0003 | c0002 | t0030 | g0106 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02809 | hp1 | a0001 | c0004 | t0018 | g0045 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02809 | hp2 | a0001 | c0005 | t0004 | g0011 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02818 | hp2 | a0001 | c0005 | t0004 | g0137 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02886 | hp1 | a0003 | c0025 | t0002 | g0142 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02886 | hp2 | a0001 | c0004 | t0003 | g0067 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02895 | hp1 | a0012 | c0015 | t0003 | g0052 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02895 | hp2 | a0001 | c0005 | t0004 | g0118 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02896 | hp1 | a0001 | c0004 | t0003 | g0146 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02896 | hp2 | a0010 | c0012 | t0014 | g0262 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02897 | hp1 | a0012 | c0015 | t0003 | g0051 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02897 | hp2 | a0001 | c0004 | t0003 | g0026 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0076 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02922 | hp2 | a0019 | c0034 | t0001 | g0036 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02965 | hp1 | a0001 | c0005 | t0004 | g0024 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02965 | hp2 | a0001 | c0004 | t0011 | g0048 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02970 | hp1 | a0002 | c0001 | t0001 | g0246 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02970 | hp2 | a0020 | c0037 | t0001 | g0250 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0039 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02976 | hp2 | a0001 | c0008 | t0008 | g0027 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0183 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03017 | hp2 | a0003 | c0002 | t0002 | g0010 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03041 | hp1 | a0001 | c0008 | t0007 | g0014 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03041 | hp2 | a0001 | c0005 | t0004 | g0138 | AFR | GWD | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03098 | hp1 | a0001 | c0026 | t0013 | g0260 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03098 | hp2 | a0001 | c0005 | t0004 | g0011 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03130 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03130 | hp2 | a0002 | c0001 | t0001 | g0039 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03195 | hp1 | a0002 | c0001 | t0001 | g0258 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03195 | hp2 | a0001 | c0005 | t0004 | g0136 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03209 | hp1 | a0011 | c0017 | t0001 | g0042 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03209 | hp2 | a0001 | c0005 | t0004 | g0024 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0257 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03239 | hp1 | a0003 | c0002 | t0002 | g0010 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03239 | hp2 | a0001 | c0003 | t0010 | g0002 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03453 | hp2 | a0001 | c0004 | t0003 | g0073 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0011 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03486 | hp2 | a0001 | c0004 | t0028 | g0049 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0239 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03516 | hp2 | a0001 | c0004 | t0003 | g0147 | AFR | ESN | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03579 | hp1 | a0001 | c0004 | t0003 | g0152 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03579 | hp2 | a0001 | c0005 | t0004 | g0025 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03654 | hp1 | a0001 | c0004 | t0003 | g0053 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03654 | hp2 | a0001 | c0004 | t0003 | g0060 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03669 | hp1 | a0003 | c0002 | t0002 | g0001 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03688 | hp1 | a0001 | c0003 | t0010 | g0017 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03688 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03704 | hp1 | a0021 | c0022 | t0002 | g0094 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03704 | hp2 | a0001 | c0005 | t0004 | g0123 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03710 | hp1 | a0001 | c0004 | t0003 | g0075 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03710 | hp2 | a0003 | c0002 | t0002 | g0144 | SAS | PJL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03834 | hp1 | a0003 | c0002 | t0002 | g0107 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03927 | hp1 | a0003 | c0002 | t0002 | g0010 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0187 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03942 | hp1 | a0001 | c0004 | t0003 | g0064 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03942 | hp2 | a0003 | c0002 | t0002 | g0111 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0202 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04115 | hp2 | a0003 | c0002 | t0002 | g0010 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04184 | hp1 | a0001 | c0003 | t0023 | g0006 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04184 | hp2 | a0022 | c0033 | t0001 | g0230 | SAS | BEB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0009 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04199 | hp2 | a0003 | c0002 | t0002 | g0001 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04204 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04204 | hp2 | a0003 | c0002 | t0002 | g0001 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04228 | hp1 | a0003 | c0002 | t0002 | g0001 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG04228 | hp2 | a0001 | c0005 | t0004 | g0117 | SAS | STU | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18522 | hp2 | a0001 | c0005 | t0025 | g0133 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18747 | hp2 | a0023 | c0024 | t0005 | g0171 | EAS | CHB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0255 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18941 | hp1 | a0004 | c0006 | t0005 | g0179 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0210 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18942 | hp2 | a0003 | c0002 | t0002 | g0108 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18943 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18943 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18944 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18944 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18945 | hp1 | a0003 | c0002 | t0002 | g0082 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18945 | hp2 | a0004 | c0006 | t0005 | g0015 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18946 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18946 | hp2 | a0003 | c0002 | t0002 | g0101 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18947 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18947 | hp2 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18948 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18949 | hp1 | a0004 | c0010 | t0005 | g0165 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18950 | hp1 | a0004 | c0006 | t0005 | g0178 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18950 | hp2 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18951 | hp1 | a0001 | c0004 | t0003 | g0007 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18951 | hp2 | a0003 | c0002 | t0012 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18952 | hp1 | a0005 | c0007 | t0001 | g0196 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18952 | hp2 | a0004 | c0006 | t0005 | g0160 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18953 | hp1 | a0003 | c0002 | t0002 | g0145 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18954 | hp1 | a0004 | c0006 | t0005 | g0172 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18954 | hp2 | a0003 | c0002 | t0002 | g0087 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18956 | hp1 | a0003 | c0002 | t0002 | g0099 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18956 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18959 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18959 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18960 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18960 | hp2 | a0004 | c0006 | t0005 | g0176 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18961 | hp1 | a0003 | c0002 | t0002 | g0092 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18962 | hp1 | a0013 | c0018 | t0004 | g0012 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18965 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18965 | hp2 | a0004 | c0006 | t0005 | g0163 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18971 | hp1 | a0005 | c0007 | t0001 | g0192 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18975 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18975 | hp2 | a0004 | c0006 | t0005 | g0169 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18977 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18977 | hp2 | a0004 | c0006 | t0005 | g0180 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18979 | hp1 | a0001 | c0003 | t0021 | g0199 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18980 | hp1 | a0001 | c0005 | t0004 | g0012 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18982 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18982 | hp2 | a0004 | c0006 | t0005 | g0170 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18984 | hp1 | a0005 | c0007 | t0001 | g0029 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18984 | hp2 | a0024 | c0023 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18985 | hp1 | a0004 | c0006 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18985 | hp2 | a0003 | c0002 | t0002 | g0141 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18986 | hp1 | a0009 | c0011 | t0002 | g0112 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18986 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18997 | hp1 | a0003 | c0002 | t0002 | g0091 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18998 | hp1 | a0005 | c0007 | t0001 | g0193 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18998 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18999 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19001 | hp1 | a0004 | c0006 | t0005 | g0173 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19001 | hp2 | a0002 | c0001 | t0001 | g0222 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19002 | hp1 | a0001 | c0005 | t0004 | g0129 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19003 | hp2 | a0003 | c0002 | t0002 | g0105 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19004 | hp2 | a0003 | c0002 | t0012 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19005 | hp1 | a0004 | c0006 | t0005 | g0015 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0226 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19007 | hp2 | a0001 | c0003 | t0020 | g0186 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19009 | hp1 | a0001 | c0005 | t0004 | g0122 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19043 | hp1 | a0001 | c0004 | t0003 | g0062 | AFR | LWK | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0236 | AFR | LWK | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19054 | hp2 | a0004 | c0006 | t0005 | g0164 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19055 | hp1 | a0003 | c0031 | t0002 | g0116 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19055 | hp2 | a0004 | c0010 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19057 | hp1 | a0006 | c0009 | t0002 | g0093 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19057 | hp2 | a0004 | c0006 | t0005 | g0162 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19058 | hp1 | a0004 | c0006 | t0005 | g0015 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19058 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0212 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19060 | hp2 | a0003 | c0002 | t0027 | g0102 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19062 | hp2 | a0001 | c0005 | t0026 | g0125 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19063 | hp1 | a0003 | c0002 | t0002 | g0098 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19063 | hp2 | a0004 | c0006 | t0031 | g0168 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19064 | hp1 | a0003 | c0002 | t0002 | g0083 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19064 | hp2 | a0001 | c0005 | t0004 | g0013 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19067 | hp1 | a0004 | c0006 | t0005 | g0166 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19067 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19068 | hp1 | a0001 | c0005 | t0004 | g0119 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19068 | hp2 | a0005 | c0007 | t0024 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19070 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19070 | hp2 | a0006 | c0009 | t0002 | g0095 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19072 | hp1 | a0003 | c0002 | t0002 | g0090 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19072 | hp2 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19074 | hp1 | a0003 | c0002 | t0002 | g0096 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19074 | hp2 | a0004 | c0010 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19075 | hp1 | a0013 | c0018 | t0004 | g0139 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19075 | hp2 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19077 | hp1 | a0005 | c0007 | t0001 | g0189 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19077 | hp2 | a0004 | c0006 | t0005 | g0174 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19079 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19081 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19081 | hp2 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19082 | hp1 | a0025 | c0036 | t0001 | g0031 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19082 | hp2 | a0004 | c0006 | t0005 | g0167 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19085 | hp1 | a0005 | c0007 | t0001 | g0195 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19085 | hp2 | a0003 | c0002 | t0002 | g0022 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19088 | hp1 | a0004 | c0006 | t0005 | g0161 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19088 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19090 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19090 | hp2 | a0005 | c0007 | t0001 | g0188 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19091 | hp1 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19091 | hp2 | a0004 | c0006 | t0005 | g0003 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19240 | hp1 | a0001 | c0005 | t0004 | g0025 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA19240 | hp2 | a0001 | c0004 | t0018 | g0044 | AFR | YRI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20752 | hp1 | a0002 | c0001 | t0016 | g0009 | EUR | TSI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20752 | hp2 | a0003 | c0002 | t0002 | g0001 | EUR | TSI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0006 | EUR | TSI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20805 | hp2 | a0003 | c0027 | t0002 | g0100 | EUR | TSI | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20905 | hp1 | a0003 | c0002 | t0002 | g0001 | SAS | GIH | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA20905 | hp2 | a0001 | c0004 | t0003 | g0050 | SAS | GIH | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01123 | hp1 | a0001 | c0004 | t0003 | g0077 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0032 | AMR | CLM | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02109 | hp1 | a0002 | c0001 | t0001 | g0244 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02109 | hp2 | a0001 | c0004 | t0003 | g0151 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0233 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02486 | hp2 | a0002 | c0001 | t0001 | g0256 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0253 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0068 | AFR | ACB | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03471 | hp1 | a0003 | c0002 | t0002 | g0109 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG03471 | hp2 | a0001 | c0004 | t0033 | g0143 | AFR | MSL | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG06807 | hp1 | a0001 | c0005 | t0004 | g0132 | AFR | USA | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
HG06807 | hp2 | a0001 | c0004 | t0003 | g0069 | AFR | USA | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18955 | hp1 | a0001 | c0004 | t0003 | g0054 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA18955 | hp2 | a0001 | c0005 | t0004 | g0124 | EAS | JPT | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA21309 | hp1 | a0026 | c0020 | t0008 | g0153 | AFR | LWK | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
NA21309 | hp2 | a0027 | c0038 | t0001 | g0016 | AFR | LWK | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0181 | REF | REF | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
homoSapiens | grch38p0 | a0001 | c0003 | t0006 | g0020 | REF | REF | BMS1_chr10_42777795_42839937 | BMS1 | chr10 | 42777795 | 42839937 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:42784362 | G | A | 1 | a0001 | 3 | HG02602.hp1 HG03239.hp2 HG03688.hp1 |
splice_region_variant | LOW | c.-33G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/23 | chr10 | 42784362 | |||||||
chr10:42784423 | G | A | 1 | a0014 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.29G>A | p.Arg10Lys | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/23 | 98/7759 | 29/3849 | 10/1282 | chr10 | 42784423 | |||
chr10:42784557 | C | G | 1 | a0027 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.163C>G | p.Arg55Gly | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/23 | 232/7759 | 163/3849 | 55/1282 | chr10 | 42784557 | |||
chr10:42790355 | T | A | 1 | a0026 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.480T>A | p.Phe160Leu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/23 | 549/7759 | 480/3849 | 160/1282 | chr10 | 42790355 | |||
chr10:42790473 | A | G | 1 | a0016 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.598A>G | p.Lys200Glu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/23 | 667/7759 | 598/3849 | 200/1282 | chr10 | 42790473 | |||
chr10:42791700 | G | A | 1 | a0005 | 19 | HG00673.hp2 HG02040.hp2 HG02074.hp1 others(16): Show |
missense_variant | MODERATE | c.710G>A | p.Arg237His | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/23 | 779/7759 | 710/3849 | 237/1282 | chr10 | 42791700 | |||
chr10:42792494 | A | G | 1 | a0013 | 2 | NA18962.hp1 NA19075.hp1 |
missense_variant&splice_region_variant | MODERATE | c.781A>G | p.Met261Val | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 7/23 | 850/7759 | 781/3849 | 261/1282 | chr10 | 42792494 | |||
chr10:42793952 | A | T | 1 | a0011 | 2 | HG02630.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.1190A>T | p.Asp397Val | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/23 | 1259/7759 | 1190/3849 | 397/1282 | chr10 | 42793952 | |||
chr10:42793991 | G | A | 1 | a0018 | 1 | HG02602.hp2 | missense_variant&splice_region_variant | MODERATE | c.1229G>A | p.Gly410Glu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/23 | 1298/7759 | 1229/3849 | 410/1282 | chr10 | 42793991 | |||
chr10:42796499 | C | G | 1 | a0020 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1255C>G | p.Gln419Glu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1324/7759 | 1255/3849 | 419/1282 | chr10 | 42796499 | |||
chr10:42796521 | G | A | 1 | a0022 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1277G>A | p.Arg426Gln | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1346/7759 | 1277/3849 | 426/1282 | chr10 | 42796521 | |||
chr10:42796889 | G | A | 1 | a0009 | 2 | HG02056.hp2 NA18986.hp1 |
missense_variant | MODERATE | c.1645G>A | p.Ala549Thr | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1714/7759 | 1645/3849 | 549/1282 | chr10 | 42796889 | |||
chr10:42796898 | T | C | 1 | a0006 | 3 | HG02129.hp2 NA19057.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.1654T>C | p.Ser552Pro | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1723/7759 | 1654/3849 | 552/1282 | chr10 | 42796898 | |||
chr10:42796922 | C | T | 1 | a0017 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1678C>T | p.Arg560Cys | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1747/7759 | 1678/3849 | 560/1282 | chr10 | 42796922 | |||
chr10:42796923 | G | A | 1 | a0021 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1679G>A | p.Arg560His | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1748/7759 | 1679/3849 | 560/1282 | chr10 | 42796923 | |||
chr10:42797003 | G | C | 1 | a0010 | 2 | HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.1759G>C | p.Val587Leu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1828/7759 | 1759/3849 | 587/1282 | chr10 | 42797003 | |||
chr10:42797199 | A | G | 6 | a0002 a0011 a0015 others(3): Show |
87 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
missense_variant | MODERATE | c.1955A>G | p.Lys652Arg | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 2024/7759 | 1955/3849 | 652/1282 | chr10 | 42797199 | |||
chr10:42816665 | A | G | 1 | a0008 | 2 | HG01978.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.2396A>G | p.Asn799Ser | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/23 | 2465/7759 | 2396/3849 | 799/1282 | chr10 | 42816665 | |||
chr10:42817360 | G | A | 1 | a0015 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2446G>A | p.Asp816Asn | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/23 | 2515/7759 | 2446/3849 | 816/1282 | chr10 | 42817360 | |||
chr10:42817394 | A | G | 1 | a0012 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2480A>G | p.Asp827Gly | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/23 | 2549/7759 | 2480/3849 | 827/1282 | chr10 | 42817394 | |||
chr10:42820245 | G | A | 5 | a0004 a0017 a0018 others(2): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
missense_variant | MODERATE | c.2590G>A | p.Ala864Thr | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 16/23 | 2659/7759 | 2590/3849 | 864/1282 | chr10 | 42820245 | |||
chr10:42820562 | A | G | 1 | a0007 | 2 | HG01109.hp1 HG01884.hp2 |
missense_variant | MODERATE | c.2824A>G | p.Ile942Val | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/23 | 2893/7759 | 2824/3849 | 942/1282 | chr10 | 42820562 | |||
chr10:42820653 | C | T | 1 | a0023 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.2915C>T | p.Thr972Ile | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/23 | 2984/7759 | 2915/3849 | 972/1282 | chr10 | 42820653 | |||
chr10:42823717 | G | A | 1 | a0024 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.3389G>A | p.Arg1130Gln | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/23 | 3458/7759 | 3389/3849 | 1130/1282 | chr10 | 42823717 | |||
chr10:42823749 | G | A | 4 | a0003 a0006 a0009 others(1): Show |
76 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
missense_variant | MODERATE | c.3421G>A | p.Val1141Ile | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/23 | 3490/7759 | 3421/3849 | 1141/1282 | chr10 | 42823749 | |||
chr10:42830900 | A | G | 1 | a0025 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.3653A>G | p.His1218Arg | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3722/7759 | 3653/3849 | 1218/1282 | chr10 | 42830900 | |||
chr10:42830945 | A | G | 1 | a0019 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.3698A>G | p.Asn1233Ser | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3767/7759 | 3698/3849 | 1233/1282 | chr10 | 42830945 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:42785641 | T | C | 29 | a0001c0004 a0001c0005 a0001c0008 others(26): Show |
224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
synonymous_variant | LOW | c.336T>C | p.Thr112Thr | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/23 | 405/7759 | 336/3849 | 112/1282 | chr10 | 42785641 | |||
chr10:42793959 | G | A | 2 | a0001c0005 a0013c0018 |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
synonymous_variant | LOW | c.1197G>A | p.Lys399Lys | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/23 | 1266/7759 | 1197/3849 | 399/1282 | chr10 | 42793959 | |||
chr10:42796564 | A | G | 2 | a0003c0031 a0004c0010 |
4 | NA18949.hp1 NA19055.hp1 NA19055.hp2 others(1): Show |
synonymous_variant | LOW | c.1320A>G | p.Gly440Gly | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1389/7759 | 1320/3849 | 440/1282 | chr10 | 42796564 | |||
chr10:42796744 | A | G | 1 | a0001c0030 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1500A>G | p.Ala500Ala | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/23 | 1569/7759 | 1500/3849 | 500/1282 | chr10 | 42796744 | |||
chr10:42817359 | C | T | 6 | a0003c0002 a0003c0027 a0003c0031 others(3): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
synonymous_variant | LOW | c.2445C>T | p.Pro815Pro | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/23 | 2514/7759 | 2445/3849 | 815/1282 | chr10 | 42817359 | |||
chr10:42820564 | C | T | 1 | a0003c0027 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.2826C>T | p.Ile942Ile | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/23 | 2895/7759 | 2826/3849 | 942/1282 | chr10 | 42820564 | |||
chr10:42820651 | T | C | 3 | a0001c0008 a0001c0013 a0026c0020 |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
synonymous_variant | LOW | c.2913T>C | p.Tyr971Tyr | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/23 | 2982/7759 | 2913/3849 | 971/1282 | chr10 | 42820651 | |||
chr10:42823652 | G | A | 1 | a0010c0012 | 2 | HG02572.hp1 HG02896.hp2 |
synonymous_variant | LOW | c.3324G>A | p.Ala1108Ala | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/23 | 3393/7759 | 3324/3849 | 1108/1282 | chr10 | 42823652 | |||
chr10:42830350 | C | T | 1 | a0001c0026 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.3546C>T | p.Thr1182Thr | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 22/23 | 3615/7759 | 3546/3849 | 1182/1282 | chr10 | 42830350 | |||
chr10:42831081 | G | A | 1 | a0001c0013 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.3834G>A | p.Glu1278Glu | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3903/7759 | 3834/3849 | 1278/1282 | chr10 | 42831081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:42831179 | A | C | 33 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0018 others(30): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*83A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 83 | chr10 | 42831179 | ||||||
chr10:42831417 | G | C | 4 | a0001c0005t0004 a0001c0005t0025 a0001c0005t0026 others(1): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 321 | chr10 | 42831417 | ||||||
chr10:42831561 | TTTTTG | T | 18 | a0001c0004t0003 a0001c0004t0033 a0001c0005t0004 others(15): Show |
121 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*475_*479delGTTTT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 475 | INFO_REALIGN_3_PRIME | chr10 | 42831561 | |||||
chr10:42832057 | G | A | 41 | a0001c0003t0020 a0001c0004t0003 a0001c0004t0011 others(38): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*961G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 961 | chr10 | 42832057 | ||||||
chr10:42832096 | A | C | 1 | a0001c0005t0026 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1000 | chr10 | 42832096 | ||||||
chr10:42832122 | G | T | 1 | a0003c0002t0030 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1026 | chr10 | 42832122 | ||||||
chr10:42832193 | G | A | 1 | a0001c0003t0009 | 4 | HG01168.hp1 HG01169.hp1 HG01516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1097 | chr10 | 42832193 | ||||||
chr10:42832220 | T | G | 1 | a0003c0002t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1124T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1124 | chr10 | 42832220 | ||||||
chr10:42832349 | T | C | 40 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0018 others(37): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1253T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1253 | chr10 | 42832349 | ||||||
chr10:42832424 | CA | C | 59 | a0001c0003t0001 a0001c0003t0009 a0001c0003t0010 others(56): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*1340delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1340 | INFO_REALIGN_3_PRIME | chr10 | 42832424 | |||||
chr10:42832524 | T | G | 1 | a0002c0001t0016 | 2 | HG01099.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1428T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1428 | chr10 | 42832524 | ||||||
chr10:42832543 | A | G | 7 | a0004c0006t0005 a0004c0006t0031 a0004c0010t0005 others(4): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1447A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1447 | chr10 | 42832543 | ||||||
chr10:42832583 | G | A | 1 | a0001c0008t0019 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1487G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1487 | chr10 | 42832583 | ||||||
chr10:42832589 | T | C | 40 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0018 others(37): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1493T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1493 | chr10 | 42832589 | ||||||
chr10:42832862 | C | A | 1 | a0002c0001t0017 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1766C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1766 | chr10 | 42832862 | ||||||
chr10:42832902 | A | T | 1 | a0005c0007t0024 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1806A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1806 | chr10 | 42832902 | ||||||
chr10:42833058 | A | G | 3 | a0001c0004t0003 a0012c0015t0003 a0014c0019t0003 |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1962A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 1962 | chr10 | 42833058 | ||||||
chr10:42833107 | A | G | 1 | a0001c0008t0015 | 2 | HG00735.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2011A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2011 | chr10 | 42833107 | ||||||
chr10:42833249 | G | C | 1 | a0001c0005t0025 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2153G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2153 | chr10 | 42833249 | ||||||
chr10:42833272 | A | C | 2 | a0001c0008t0007 a0001c0008t0019 |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2176A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2176 | chr10 | 42833272 | ||||||
chr10:42833404 | G | A | 1 | a0001c0030t0032 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2308 | chr10 | 42833404 | ||||||
chr10:42833489 | C | CT | 38 | a0001c0004t0003 a0001c0004t0018 a0001c0004t0028 others(35): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*2394dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2395 | INFO_REALIGN_3_PRIME | chr10 | 42833489 | |||||
chr10:42833490 | TATGG | T | 2 | a0001c0004t0011 a0007c0014t0011 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2395_*2398delATGG | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2395 | chr10 | 42833490 | ||||||
chr10:42833590 | G | A | 7 | a0004c0006t0005 a0004c0006t0031 a0004c0010t0005 others(4): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2494G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2494 | chr10 | 42833590 | ||||||
chr10:42833740 | T | C | 2 | a0001c0004t0018 a0001c0004t0029 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2644T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2644 | chr10 | 42833740 | ||||||
chr10:42834081 | T | C | 1 | a0001c0003t0021 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2985T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 2985 | chr10 | 42834081 | ||||||
chr10:42834170 | G | A | 1 | a0001c0004t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3074G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3074 | chr10 | 42834170 | ||||||
chr10:42834208 | G | T | 1 | a0001c0004t0033 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3112G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3112 | chr10 | 42834208 | ||||||
chr10:42834244 | GTTTTC | G | 9 | a0001c0004t0003 a0001c0008t0007 a0001c0008t0008 others(6): Show |
59 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3153_*3157delCTTT others(1): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3153 | INFO_REALIGN_3_PRIME | chr10 | 42834244 | |||||
chr10:42834291 | T | G | 1 | a0003c0002t0012 | 3 | HG02155.hp1 NA18951.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3195T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3195 | chr10 | 42834291 | ||||||
chr10:42834322 | A | G | 7 | a0004c0006t0005 a0004c0006t0031 a0004c0010t0005 others(4): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3226A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3226 | chr10 | 42834322 | ||||||
chr10:42834381 | T | C | 1 | a0002c0001t0022 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3285T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3285 | chr10 | 42834381 | ||||||
chr10:42834396 | GA | G | 40 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0018 others(37): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*3305delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3305 | INFO_REALIGN_3_PRIME | chr10 | 42834396 | |||||
chr10:42834430 | G | A | 34 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0018 others(31): Show |
206 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*3334G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3334 | chr10 | 42834430 | ||||||
chr10:42834579 | C | T | 1 | a0001c0003t0023 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3483C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3483 | chr10 | 42834579 | ||||||
chr10:42834628 | GT | G | 4 | a0001c0005t0004 a0001c0005t0025 a0001c0005t0026 others(1): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3536delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 23/23 | 3536 | INFO_REALIGN_3_PRIME | chr10 | 42834628 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:42782834 | C | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
splice_region_variant&intron_variant | LOW | c.-34+4C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42782834 | |||||||
chr10:42782926 | G | C | 2 | a0007c0014t0011g0040 a0007c0014t0011g0041 |
2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-34+96G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42782926 | |||||||
chr10:42782927 | G | A | 1 | a0011c0017t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-34+97G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42782927 | |||||||
chr10:42782936 | G | T | 1 | a0001c0026t0013g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-34+106G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42782936 | |||||||
chr10:42783086 | T | C | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-34+256T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783086 | |||||||
chr10:42783120 | C | T | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.-34+290C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783120 | |||||||
chr10:42783169 | G | A | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-34+339G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783169 | |||||||
chr10:42783211 | C | T | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.-34+381C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783211 | |||||||
chr10:42783388 | A | G | 1 | a0001c0004t0003g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+558A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783388 | |||||||
chr10:42783561 | C | CT | 8 | a0001c0004t0003g0026 a0001c0004t0003g0146 a0001c0004t0003g0147 others(5): Show |
9 | HG01106.hp1 HG01167.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+742dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr10 | 42783561 | ||||||
chr10:42783739 | A | T | 1 | a0003c0002t0002g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-33-623A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783739 | |||||||
chr10:42783755 | A | G | 2 | a0001c0008t0015g0158 a0001c0008t0015g0159 |
2 | HG00735.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-33-607A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783755 | |||||||
chr10:42783914 | T | C | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-448T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783914 | |||||||
chr10:42783917 | A | G | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-445A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42783917 | |||||||
chr10:42784002 | T | G | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-33-360T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42784002 | |||||||
chr10:42784024 | G | T | 150 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(147): Show |
201 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-33-338G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42784024 | |||||||
chr10:42784145 | C | T | 1 | a0001c0013t0008g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-33-217C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42784145 | |||||||
chr10:42784354 | C | T | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.-33-8C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 1/22 | chr10 | 42784354 | |||||||
chr10:42784671 | C | A | 1 | a0002c0001t0001g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.176+101C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784671 | |||||||
chr10:42784737 | C | T | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.176+167C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784737 | |||||||
chr10:42784842 | A | C | 6 | a0002c0001t0001g0039 a0002c0001t0001g0255 a0002c0001t0001g0256 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.176+272A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784842 | |||||||
chr10:42784865 | A | G | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.176+295A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784865 | |||||||
chr10:42784873 | C | T | 1 | a0003c0002t0002g0141 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.176+303C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784873 | |||||||
chr10:42784901 | A | G | 30 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(27): Show |
37 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(34): Show |
intron_variant | MODIFIER | c.176+331A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42784901 | |||||||
chr10:42785114 | C | T | 1 | a0001c0005t0004g0140 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.177-368C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785114 | |||||||
chr10:42785132 | C | T | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.177-350C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785132 | |||||||
chr10:42785148 | C | T | 30 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(27): Show |
37 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(34): Show |
intron_variant | MODIFIER | c.177-334C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785148 | |||||||
chr10:42785205 | A | G | 151 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(148): Show |
202 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.177-277A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785205 | |||||||
chr10:42785275 | A | G | 1 | a0003c0002t0002g0023 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.177-207A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785275 | |||||||
chr10:42785382 | A | G | 5 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(2): Show |
7 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.177-100A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785382 | |||||||
chr10:42785388 | G | A | 1 | a0002c0001t0001g0183 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.177-94G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785388 | |||||||
chr10:42785461 | T | C | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.177-21T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785461 | |||||||
chr10:42785471 | T | G | 1 | a0001c0026t0013g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177-11T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 2/22 | chr10 | 42785471 | |||||||
chr10:42785705 | G | A | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.367+33G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42785705 | |||||||
chr10:42785735 | C | A | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.367+63C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42785735 | |||||||
chr10:42785979 | C | T | 1 | a0002c0001t0001g0254 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.367+307C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42785979 | |||||||
chr10:42785987 | G | A | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.367+315G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42785987 | |||||||
chr10:42786083 | C | G | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.367+411C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786083 | |||||||
chr10:42786155 | C | T | 7 | a0001c0004t0003g0026 a0001c0004t0003g0146 a0001c0004t0003g0147 others(4): Show |
8 | HG01106.hp1 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+483C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786155 | |||||||
chr10:42786417 | A | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.367+745A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786417 | |||||||
chr10:42786471 | G | C | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.368-697G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786471 | |||||||
chr10:42786563 | C | T | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.368-605C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786563 | |||||||
chr10:42786619 | T | A | 1 | a0003c0002t0002g0010 | 4 | HG03017.hp2 HG03239.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-549T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786619 | |||||||
chr10:42786779 | T | G | 1 | a0001c0005t0004g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.368-389T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786779 | |||||||
chr10:42786906 | C | CAGTCAGA others(31): Show |
1 | a0004c0006t0005g0160 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.368-261_368-224dup others(38): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr10 | 42786906 | ||||||
chr10:42786971 | T | G | 1 | a0001c0003t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.368-197T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42786971 | |||||||
chr10:42787048 | T | C | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368-120T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42787048 | |||||||
chr10:42787080 | A | G | 47 | a0003c0002t0002g0001 a0003c0002t0002g0010 a0003c0002t0002g0022 others(44): Show |
76 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.368-88A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42787080 | |||||||
chr10:42787081 | T | C | 1 | a0003c0002t0002g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.368-87T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 3/22 | chr10 | 42787081 | |||||||
chr10:42787305 | T | G | 1 | a0002c0001t0001g0185 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.447+58T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787305 | |||||||
chr10:42787315 | G | A | 46 | a0003c0002t0002g0001 a0003c0002t0002g0010 a0003c0002t0002g0022 others(43): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.447+68G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787315 | |||||||
chr10:42787374 | C | T | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.447+127C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787374 | |||||||
chr10:42787380 | A | G | 2 | a0003c0002t0002g0115 a0003c0031t0002g0116 |
2 | HG00558.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.447+133A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787380 | |||||||
chr10:42787419 | T | C | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+172T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787419 | |||||||
chr10:42787495 | A | G | 1 | a0001c0026t0013g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.447+248A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787495 | |||||||
chr10:42787497 | C | A | 3 | a0001c0005t0004g0011 a0001c0005t0004g0024 a0001c0005t0004g0118 |
6 | HG02809.hp2 HG02895.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+250C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787497 | |||||||
chr10:42787536 | A | G | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.447+289A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787536 | |||||||
chr10:42787538 | A | G | 2 | a0001c0004t0003g0076 a0001c0004t0003g0077 |
2 | HG01123.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.447+291A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787538 | |||||||
chr10:42787578 | T | C | 30 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(27): Show |
37 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(34): Show |
intron_variant | MODIFIER | c.447+331T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787578 | |||||||
chr10:42787618 | A | G | 1 | a0001c0004t0003g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.447+371A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787618 | |||||||
chr10:42787838 | C | T | 1 | a0003c0002t0002g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.447+591C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787838 | |||||||
chr10:42787945 | A | G | 79 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(76): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.447+698A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42787945 | |||||||
chr10:42788044 | G | A | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.447+797G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788044 | |||||||
chr10:42788049 | CAA | C | 79 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(76): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.447+804_447+805del others(2): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42788049 | ||||||
chr10:42788150 | CTAAA | C | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.447+907_447+910del others(4): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42788150 | ||||||
chr10:42788214 | C | T | 2 | a0009c0011t0002g0112 a0009c0011t0002g0113 |
2 | HG02056.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.447+967C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788214 | |||||||
chr10:42788232 | A | T | 4 | a0001c0004t0003g0071 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
4 | HG01099.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+985A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788232 | |||||||
chr10:42788271 | G | T | 1 | a0002c0001t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.447+1024G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788271 | |||||||
chr10:42788306 | C | T | 219 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(216): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.447+1059C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788306 | |||||||
chr10:42788316 | T | C | 1 | a0002c0001t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.447+1069T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788316 | |||||||
chr10:42788338 | T | C | 1 | a0001c0004t0003g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.447+1091T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788338 | |||||||
chr10:42788480 | T | G | 1 | a0002c0001t0001g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.447+1233T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788480 | |||||||
chr10:42788583 | TTATTC | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.447+1339_447+1343d others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42788583 | ||||||
chr10:42788678 | T | C | 1 | a0002c0001t0001g0206 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.447+1431T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788678 | |||||||
chr10:42788722 | C | T | 1 | a0001c0004t0003g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.447+1475C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788722 | |||||||
chr10:42788769 | G | A | 1 | a0001c0003t0020g0186 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.447+1522G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788769 | |||||||
chr10:42788931 | G | T | 1 | a0004c0006t0005g0180 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.448-1392G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788931 | |||||||
chr10:42788935 | ATAATCAG others(4): Show |
A | 1 | a0003c0002t0002g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448-1385_448-1375d others(13): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42788935 | ||||||
chr10:42788941 | A | G | 3 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0178 |
3 | NA18950.hp1 NA18986.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.448-1382A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42788941 | |||||||
chr10:42789072 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.448-1251A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789072 | |||||||
chr10:42789187 | C | G | 1 | a0001c0005t0004g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.448-1136C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789187 | |||||||
chr10:42789311 | A | G | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.448-1012A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789311 | |||||||
chr10:42789342 | A | G | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.448-981A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789342 | |||||||
chr10:42789394 | G | A | 18 | a0001c0005t0004g0012 a0001c0005t0004g0013 a0001c0005t0004g0117 others(15): Show |
21 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.448-929G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789394 | |||||||
chr10:42789408 | A | AT | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.448-907dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42789408 | ||||||
chr10:42789432 | C | T | 1 | a0001c0003t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.448-891C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789432 | |||||||
chr10:42789498 | A | C | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-825A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789498 | |||||||
chr10:42789592 | GT | G | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.448-720delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr10 | 42789592 | ||||||
chr10:42789961 | C | T | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.448-362C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42789961 | |||||||
chr10:42790145 | T | C | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-178T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42790145 | |||||||
chr10:42790173 | T | C | 2 | a0003c0002t0002g0080 a0003c0002t0002g0081 |
2 | HG00544.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.448-150T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42790173 | |||||||
chr10:42790265 | T | C | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.448-58T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 4/22 | chr10 | 42790265 | |||||||
chr10:42790575 | C | T | 1 | a0009c0011t0002g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.636+64C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42790575 | |||||||
chr10:42790647 | G | C | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.636+136G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42790647 | |||||||
chr10:42790718 | C | T | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.636+207C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42790718 | |||||||
chr10:42790719 | G | A | 2 | a0012c0015t0003g0051 a0012c0015t0003g0052 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.636+208G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42790719 | |||||||
chr10:42790722 | C | T | 1 | a0001c0003t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.636+211C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42790722 | |||||||
chr10:42790850 | CA | C | 27 | a0001c0030t0032g0043 a0004c0006t0005g0003 a0004c0006t0005g0015 others(24): Show |
36 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.636+351delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr10 | 42790850 | ||||||
chr10:42791157 | G | A | 4 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(1): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-470G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791157 | |||||||
chr10:42791189 | G | A | 1 | a0001c0005t0004g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.637-438G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791189 | |||||||
chr10:42791209 | G | A | 4 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(1): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-418G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791209 | |||||||
chr10:42791236 | C | T | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.637-391C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791236 | |||||||
chr10:42791248 | G | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-379G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791248 | |||||||
chr10:42791379 | T | G | 2 | a0007c0014t0011g0040 a0007c0014t0011g0041 |
2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.637-248T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791379 | |||||||
chr10:42791410 | C | G | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.637-217C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791410 | |||||||
chr10:42791426 | G | C | 4 | a0001c0026t0013g0260 a0001c0030t0032g0043 a0008c0016t0013g0046 others(1): Show |
4 | HG01978.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-201G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791426 | |||||||
chr10:42791438 | G | A | 1 | a0003c0002t0002g0082 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.637-189G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791438 | |||||||
chr10:42791476 | A | G | 154 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(151): Show |
205 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.637-151A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791476 | |||||||
chr10:42791579 | A | G | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-48A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 5/22 | chr10 | 42791579 | |||||||
chr10:42791836 | G | A | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.779+67G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42791836 | |||||||
chr10:42791912 | T | C | 1 | a0001c0004t0003g0053 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.779+143T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42791912 | |||||||
chr10:42791975 | G | A | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.779+206G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42791975 | |||||||
chr10:42792088 | C | G | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.779+319C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42792088 | |||||||
chr10:42792114 | C | T | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.779+345C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42792114 | |||||||
chr10:42792149 | A | T | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.780-344A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42792149 | |||||||
chr10:42792257 | G | A | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.780-236G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42792257 | |||||||
chr10:42792441 | G | T | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.780-52G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 6/22 | chr10 | 42792441 | |||||||
chr10:42793157 | C | T | 4 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(1): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+13C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793157 | |||||||
chr10:42793178 | T | G | 25 | a0001c0003t0001g0002 a0001c0003t0001g0016 a0001c0003t0001g0017 others(22): Show |
36 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1089+34T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793178 | |||||||
chr10:42793194 | A | C | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1089+50A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793194 | |||||||
chr10:42793278 | A | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1089+134A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793278 | |||||||
chr10:42793368 | A | G | 26 | a0001c0003t0001g0002 a0001c0003t0001g0016 a0001c0003t0001g0017 others(23): Show |
37 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1089+224A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793368 | |||||||
chr10:42793414 | A | C | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1089+270A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793414 | |||||||
chr10:42793502 | T | C | 39 | a0002c0001t0001g0004 a0002c0001t0001g0005 a0002c0001t0001g0008 others(36): Show |
63 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1090-350T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793502 | |||||||
chr10:42793812 | T | C | 3 | a0001c0026t0013g0260 a0008c0016t0013g0046 a0008c0016t0013g0047 |
3 | HG01978.hp1 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1090-40T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793812 | |||||||
chr10:42793826 | G | A | 1 | a0003c0002t0002g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1090-26G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 8/22 | chr10 | 42793826 | |||||||
chr10:42794122 | T | C | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1229+131T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794122 | |||||||
chr10:42794200 | A | C | 155 | a0001c0003t0020g0186 a0001c0004t0003g0007 a0001c0004t0003g0021 others(152): Show |
206 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1229+209A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794200 | |||||||
chr10:42794286 | C | G | 5 | a0001c0003t0001g0038 a0001c0003t0001g0249 a0001c0003t0001g0251 others(2): Show |
6 | HG02572.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229+295C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794286 | |||||||
chr10:42794415 | A | G | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1229+424A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794415 | |||||||
chr10:42794457 | T | C | 3 | a0001c0004t0003g0021 a0001c0004t0003g0076 a0001c0004t0003g0077 |
4 | HG01123.hp1 HG01192.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1229+466T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794457 | |||||||
chr10:42794469 | T | A | 9 | a0002c0001t0001g0004 a0002c0001t0001g0207 a0002c0001t0001g0208 others(6): Show |
18 | HG00438.hp1 HG00597.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1229+478T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794469 | |||||||
chr10:42794576 | G | C | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1229+585G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794576 | |||||||
chr10:42794577 | C | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1229+586C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794577 | |||||||
chr10:42794664 | T | G | 1 | a0011c0017t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1229+673T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794664 | |||||||
chr10:42794764 | C | CT | 41 | a0001c0003t0001g0200 a0002c0001t0001g0004 a0002c0001t0001g0005 others(38): Show |
65 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1229+784dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr10 | 42794764 | ||||||
chr10:42794764 | CT | C | 8 | a0001c0004t0011g0048 a0001c0026t0013g0260 a0001c0030t0032g0043 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1229+784delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr10 | 42794764 | ||||||
chr10:42794766 | T | C | 1 | a0001c0003t0001g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1229+775T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794766 | |||||||
chr10:42794891 | C | T | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1229+900C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42794891 | |||||||
chr10:42795032 | T | C | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+1041T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795032 | |||||||
chr10:42795097 | C | T | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+1106C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795097 | |||||||
chr10:42795098 | C | A | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+1107C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795098 | |||||||
chr10:42795133 | T | C | 61 | a0002c0001t0001g0004 a0002c0001t0001g0005 a0002c0001t0001g0008 others(58): Show |
87 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1229+1142T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795133 | |||||||
chr10:42795135 | T | G | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+1144T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795135 | |||||||
chr10:42795152 | C | G | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+1161C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795152 | |||||||
chr10:42795486 | AT | A | 7 | a0001c0004t0003g0054 a0001c0004t0011g0048 a0002c0001t0001g0239 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230-973delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr10 | 42795486 | ||||||
chr10:42795504 | A | G | 3 | a0001c0026t0013g0260 a0008c0016t0013g0046 a0008c0016t0013g0047 |
3 | HG01978.hp1 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1230-970A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795504 | |||||||
chr10:42795528 | C | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1230-946C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795528 | |||||||
chr10:42795547 | C | T | 4 | a0001c0026t0013g0260 a0001c0030t0032g0043 a0008c0016t0013g0046 others(1): Show |
4 | HG01978.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230-927C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795547 | |||||||
chr10:42795595 | A | G | 1 | a0001c0005t0004g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1230-879A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795595 | |||||||
chr10:42795647 | G | A | 5 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(2): Show |
7 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230-827G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795647 | |||||||
chr10:42795761 | T | A | 2 | a0002c0001t0001g0207 a0002c0001t0001g0208 |
2 | NA19072.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1230-713T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795761 | |||||||
chr10:42795823 | T | G | 1 | a0002c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1230-651T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795823 | |||||||
chr10:42795833 | G | A | 1 | a0006c0009t0002g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1230-641G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42795833 | |||||||
chr10:42796192 | T | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1230-282T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42796192 | |||||||
chr10:42796193 | C | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1230-281C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42796193 | |||||||
chr10:42796227 | GT | G | 2 | a0001c0003t0001g0016 a0027c0038t0001g0016 |
3 | HG00639.hp1 HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1230-241delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr10 | 42796227 | ||||||
chr10:42796364 | A | C | 1 | a0004c0006t0005g0179 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1230-110A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42796364 | |||||||
chr10:42796413 | A | G | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1230-61A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 9/22 | chr10 | 42796413 | |||||||
chr10:42797263 | A | G | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1987+32A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/22 | chr10 | 42797263 | |||||||
chr10:42797348 | G | A | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1988-74G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/22 | chr10 | 42797348 | |||||||
chr10:42797382 | A | G | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1988-40A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 10/22 | chr10 | 42797382 | |||||||
chr10:42797601 | G | A | 1 | a0003c0002t0002g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2089+78G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42797601 | |||||||
chr10:42797909 | G | T | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2089+386G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42797909 | |||||||
chr10:42798031 | A | G | 6 | a0002c0001t0001g0039 a0002c0001t0001g0255 a0002c0001t0001g0256 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-437A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798031 | |||||||
chr10:42798136 | C | G | 1 | a0002c0001t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2090-332C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798136 | |||||||
chr10:42798143 | G | T | 1 | a0001c0005t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2090-325G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798143 | |||||||
chr10:42798154 | A | G | 25 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(22): Show |
34 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.2090-314A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798154 | |||||||
chr10:42798170 | C | A | 1 | a0001c0003t0001g0249 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2090-298C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798170 | |||||||
chr10:42798235 | G | A | 2 | a0003c0002t0002g0080 a0003c0002t0002g0081 |
2 | HG00544.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.2090-233G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798235 | |||||||
chr10:42798356 | A | C | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2090-112A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 11/22 | chr10 | 42798356 | |||||||
chr10:42798636 | G | T | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2247+11G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42798636 | |||||||
chr10:42798675 | T | C | 1 | a0002c0001t0001g0215 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2247+50T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42798675 | |||||||
chr10:42798725 | A | C | 2 | a0003c0002t0002g0109 a0003c0002t0002g0110 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2247+100A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42798725 | |||||||
chr10:42798822 | A | G | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2247+197A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42798822 | |||||||
chr10:42798934 | A | G | 1 | a0001c0005t0004g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2247+309A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42798934 | |||||||
chr10:42799021 | C | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2247+396C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799021 | |||||||
chr10:42799126 | A | G | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2247+501A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799126 | |||||||
chr10:42799311 | T | C | 3 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 |
4 | HG00735.hp1 HG01243.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+686T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799311 | |||||||
chr10:42799435 | C | T | 1 | a0022c0033t0001g0230 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2247+810C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799435 | |||||||
chr10:42799446 | A | G | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2247+821A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799446 | |||||||
chr10:42799836 | C | G | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2247+1211C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799836 | |||||||
chr10:42799995 | C | T | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+1370C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42799995 | |||||||
chr10:42800289 | G | T | 1 | a0003c0002t0002g0108 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2247+1664G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800289 | |||||||
chr10:42800441 | G | A | 2 | a0001c0004t0003g0026 a0001c0004t0003g0146 |
3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2248-1696G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800441 | |||||||
chr10:42800443 | A | G | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2248-1694A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800443 | |||||||
chr10:42800525 | A | AT | 14 | a0001c0003t0001g0036 a0001c0003t0001g0237 a0001c0003t0001g0238 others(11): Show |
15 | HG00408.hp2 HG01123.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2248-1593dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr10 | 42800525 | ||||||
chr10:42800525 | AT | A | 46 | a0001c0003t0001g0187 a0001c0003t0006g0201 a0003c0002t0002g0001 others(43): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2248-1593delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr10 | 42800525 | ||||||
chr10:42800570 | A | G | 1 | a0001c0005t0004g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2248-1567A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800570 | |||||||
chr10:42800676 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2248-1461A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800676 | |||||||
chr10:42800731 | G | A | 1 | a0006c0009t0002g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2248-1406G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800731 | |||||||
chr10:42800892 | T | G | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2248-1245T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800892 | |||||||
chr10:42800929 | G | T | 1 | a0001c0003t0001g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2248-1208G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800929 | |||||||
chr10:42800996 | T | C | 3 | a0002c0001t0001g0248 a0002c0001t0017g0242 a0002c0001t0017g0243 |
3 | HG01167.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2248-1141T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42800996 | |||||||
chr10:42801071 | G | A | 1 | a0002c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2248-1066G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801071 | |||||||
chr10:42801072 | C | A | 1 | a0002c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2248-1065C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801072 | |||||||
chr10:42801073 | G | A | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2248-1064G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801073 | |||||||
chr10:42801105 | T | C | 1 | a0004c0006t0005g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2248-1032T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801105 | |||||||
chr10:42801138 | C | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2248-999C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801138 | |||||||
chr10:42801220 | A | G | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2248-917A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801220 | |||||||
chr10:42801237 | A | G | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2248-900A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801237 | |||||||
chr10:42801509 | C | T | 4 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 others(1): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2248-628C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801509 | |||||||
chr10:42801710 | A | G | 4 | a0001c0003t0001g0036 a0001c0003t0001g0237 a0001c0003t0001g0238 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-427A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801710 | |||||||
chr10:42801742 | G | A | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2248-395G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801742 | |||||||
chr10:42801757 | G | T | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2248-380G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801757 | |||||||
chr10:42801824 | G | A | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2248-313G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801824 | |||||||
chr10:42801891 | G | C | 2 | a0002c0001t0001g0207 a0002c0001t0001g0208 |
2 | NA19072.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2248-246G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42801891 | |||||||
chr10:42802116 | G | A | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2248-21G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 12/22 | chr10 | 42802116 | |||||||
chr10:42802283 | T | C | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2329+65T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802283 | |||||||
chr10:42802298 | T | C | 18 | a0001c0004t0003g0007 a0001c0004t0003g0050 a0001c0004t0003g0053 others(15): Show |
22 | HG01070.hp1 HG01081.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.2329+80T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802298 | |||||||
chr10:42802322 | A | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+104A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802322 | |||||||
chr10:42802402 | T | C | 2 | a0001c0004t0003g0050 a0001c0004t0003g0055 |
2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2329+184T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802402 | |||||||
chr10:42802416 | C | T | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2329+198C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802416 | |||||||
chr10:42802467 | G | C | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+249G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802467 | |||||||
chr10:42802647 | A | G | 1 | a0004c0006t0005g0175 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2329+429A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802647 | |||||||
chr10:42802724 | T | A | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2329+506T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802724 | |||||||
chr10:42802797 | AAT | A | 27 | a0003c0025t0002g0142 a0004c0006t0005g0003 a0004c0006t0005g0015 others(24): Show |
36 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.2329+581_2329+582d others(4): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42802797 | ||||||
chr10:42802800 | A | T | 27 | a0003c0025t0002g0142 a0004c0006t0005g0003 a0004c0006t0005g0015 others(24): Show |
36 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.2329+582A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42802800 | |||||||
chr10:42803225 | A | G | 2 | a0008c0016t0013g0046 a0008c0016t0013g0047 |
2 | HG01978.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2329+1007A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803225 | |||||||
chr10:42803564 | C | T | 1 | a0002c0001t0001g0183 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2329+1346C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803564 | |||||||
chr10:42803575 | T | C | 1 | a0003c0002t0002g0086 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2329+1357T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803575 | |||||||
chr10:42803590 | C | A | 1 | a0004c0006t0005g0163 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2329+1372C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803590 | |||||||
chr10:42803635 | T | C | 8 | a0002c0001t0001g0039 a0002c0001t0001g0244 a0002c0001t0001g0245 others(5): Show |
9 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2329+1417T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803635 | |||||||
chr10:42803660 | C | T | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+1442C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803660 | |||||||
chr10:42803702 | C | T | 1 | a0001c0005t0004g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2329+1484C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803702 | |||||||
chr10:42803704 | G | T | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+1486G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803704 | |||||||
chr10:42803817 | T | C | 3 | a0002c0001t0001g0031 a0002c0001t0001g0216 a0025c0036t0001g0031 |
3 | HG00673.hp1 NA18961.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2329+1599T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803817 | |||||||
chr10:42803847 | A | T | 2 | a0001c0008t0015g0158 a0001c0008t0015g0159 |
2 | HG00735.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2329+1629A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803847 | |||||||
chr10:42803854 | C | T | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2329+1636C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42803854 | |||||||
chr10:42804030 | G | A | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2329+1812G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804030 | |||||||
chr10:42804070 | A | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+1852A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804070 | |||||||
chr10:42804191 | T | C | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2329+1973T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804191 | |||||||
chr10:42804269 | G | T | 1 | a0001c0004t0003g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2329+2051G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804269 | |||||||
chr10:42804277 | A | T | 9 | a0001c0005t0004g0013 a0001c0005t0004g0119 a0001c0005t0004g0124 others(6): Show |
11 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2329+2059A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804277 | |||||||
chr10:42804357 | T | G | 1 | a0020c0037t0001g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2329+2139T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804357 | |||||||
chr10:42804414 | T | C | 1 | a0001c0003t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2329+2196T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804414 | |||||||
chr10:42804465 | T | G | 1 | a0001c0013t0008g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2329+2247T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804465 | |||||||
chr10:42804483 | G | A | 2 | a0011c0017t0001g0042 a0011c0017t0001g0231 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2329+2265G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804483 | |||||||
chr10:42804622 | T | C | 150 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(147): Show |
201 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2329+2404T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804622 | |||||||
chr10:42804649 | G | A | 3 | a0012c0015t0003g0051 a0012c0015t0003g0052 a0026c0020t0008g0153 |
3 | HG02895.hp1 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2329+2431G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804649 | |||||||
chr10:42804671 | T | G | 1 | a0002c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2329+2453T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804671 | |||||||
chr10:42804730 | AT | A | 163 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(160): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2329+2525delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42804730 | ||||||
chr10:42804743 | T | G | 1 | a0002c0001t0001g0254 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2329+2525T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804743 | |||||||
chr10:42804752 | G | T | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2329+2534G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804752 | |||||||
chr10:42804776 | G | A | 1 | a0004c0006t0005g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2329+2558G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804776 | |||||||
chr10:42804832 | C | T | 1 | a0001c0005t0004g0123 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2329+2614C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804832 | |||||||
chr10:42804874 | C | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2329+2656C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804874 | |||||||
chr10:42804945 | T | A | 2 | a0001c0008t0015g0158 a0001c0008t0015g0159 |
2 | HG00735.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2329+2727T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42804945 | |||||||
chr10:42805079 | A | G | 34 | a0001c0004t0033g0143 a0001c0005t0004g0011 a0001c0005t0004g0012 others(31): Show |
41 | HG01928.hp2 HG01943.hp2 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.2329+2861A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805079 | |||||||
chr10:42805146 | T | A | 1 | a0003c0002t0002g0087 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2329+2928T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805146 | |||||||
chr10:42805152 | T | C | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2329+2934T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805152 | |||||||
chr10:42805179 | G | A | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2329+2961G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805179 | |||||||
chr10:42805347 | C | T | 1 | a0004c0006t0005g0174 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2329+3129C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805347 | |||||||
chr10:42805404 | A | G | 1 | a0003c0002t0030g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2329+3186A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805404 | |||||||
chr10:42805437 | G | A | 1 | a0003c0002t0002g0088 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2329+3219G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805437 | |||||||
chr10:42805829 | T | C | 2 | a0011c0017t0001g0042 a0011c0017t0001g0231 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2329+3611T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805829 | |||||||
chr10:42805956 | C | T | 1 | a0004c0006t0005g0173 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2329+3738C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42805956 | |||||||
chr10:42806040 | G | A | 14 | a0002c0001t0001g0037 a0002c0001t0001g0039 a0002c0001t0001g0239 others(11): Show |
16 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2329+3822G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806040 | |||||||
chr10:42806124 | TTTC | T | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2329+3909_2329+391 others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806124 | ||||||
chr10:42806177 | A | G | 1 | a0001c0003t0001g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2329+3959A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806177 | |||||||
chr10:42806243 | T | C | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+4025T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806243 | |||||||
chr10:42806348 | G | C | 158 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(155): Show |
209 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.2329+4130G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806348 | |||||||
chr10:42806691 | C | T | 55 | a0002c0001t0001g0004 a0002c0001t0001g0005 a0002c0001t0001g0008 others(52): Show |
81 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2329+4473C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806691 | |||||||
chr10:42806737 | G | GA | 127 | a0001c0003t0001g0202 a0001c0003t0001g0233 a0001c0003t0001g0234 others(124): Show |
156 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.2329+4541dupA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806737 | ||||||
chr10:42806737 | G | GAA | 21 | a0001c0004t0003g0056 a0001c0004t0003g0057 a0001c0004t0003g0066 others(18): Show |
21 | HG00741.hp1 HG01261.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.2329+4540_2329+454 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806737 | ||||||
chr10:42806737 | GA | G | 12 | a0001c0008t0007g0014 a0001c0008t0007g0155 a0001c0008t0007g0157 others(9): Show |
16 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2329+4541delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806737 | ||||||
chr10:42806869 | G | GA | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2329+4660dupA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806869 | ||||||
chr10:42806869 | GA | G | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2329+4660delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42806869 | ||||||
chr10:42806891 | A | T | 1 | a0001c0003t0009g0035 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2329+4673A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806891 | |||||||
chr10:42806960 | T | C | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2329+4742T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42806960 | |||||||
chr10:42807000 | C | G | 1 | a0001c0026t0013g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2329+4782C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807000 | |||||||
chr10:42807094 | CAT | C | 6 | a0001c0005t0004g0011 a0001c0005t0004g0024 a0001c0005t0004g0118 others(3): Show |
9 | HG02145.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2329+4877_2329+487 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807094 | |||||||
chr10:42807222 | G | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+5004G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807222 | |||||||
chr10:42807293 | A | G | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2329+5075A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807293 | |||||||
chr10:42807296 | CTA | C | 3 | a0001c0026t0013g0260 a0008c0016t0013g0046 a0008c0016t0013g0047 |
3 | HG01978.hp1 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2329+5081_2329+508 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42807296 | ||||||
chr10:42807420 | C | T | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2329+5202C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807420 | |||||||
chr10:42807455 | G | T | 2 | a0001c0004t0003g0050 a0001c0004t0003g0055 |
2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2329+5237G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807455 | |||||||
chr10:42807755 | A | G | 3 | a0001c0004t0018g0044 a0001c0004t0018g0045 a0001c0004t0029g0078 |
3 | HG01891.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2329+5537A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807755 | |||||||
chr10:42807850 | T | C | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+5632T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807850 | |||||||
chr10:42807852 | GCA | G | 14 | a0001c0003t0001g0006 a0001c0003t0001g0038 a0001c0003t0001g0232 others(11): Show |
22 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2329+5637_2329+563 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42807852 | ||||||
chr10:42807863 | T | C | 3 | a0001c0008t0008g0027 a0001c0008t0015g0158 a0001c0008t0015g0159 |
4 | HG00735.hp1 HG01243.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2329+5645T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807863 | |||||||
chr10:42807926 | G | A | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+5708G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42807926 | |||||||
chr10:42808050 | A | G | 1 | a0001c0003t0001g0200 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2329+5832A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808050 | |||||||
chr10:42808122 | T | C | 2 | a0001c0003t0001g0016 a0027c0038t0001g0016 |
3 | HG00639.hp1 HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2329+5904T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808122 | |||||||
chr10:42808244 | C | A | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2329+6026C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808244 | |||||||
chr10:42808270 | TTTTA | T | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+6075_2329+607 others(8): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42808270 | ||||||
chr10:42808360 | G | A | 1 | a0003c0002t0002g0108 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2329+6142G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808360 | |||||||
chr10:42808361 | C | T | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2329+6143C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808361 | |||||||
chr10:42808362 | G | A | 1 | a0001c0003t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2329+6144G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808362 | |||||||
chr10:42808534 | C | T | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2329+6316C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808534 | |||||||
chr10:42808550 | T | C | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+6332T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808550 | |||||||
chr10:42808579 | G | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2329+6361G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808579 | |||||||
chr10:42808616 | A | G | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2329+6398A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808616 | |||||||
chr10:42808732 | G | A | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2329+6514G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808732 | |||||||
chr10:42808797 | C | A | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2329+6579C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808797 | |||||||
chr10:42808848 | A | G | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2329+6630A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42808848 | |||||||
chr10:42809195 | C | T | 1 | a0002c0028t0001g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2329+6977C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42809195 | |||||||
chr10:42809401 | A | G | 1 | a0001c0003t0001g0198 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2329+7183A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42809401 | |||||||
chr10:42809414 | C | CT | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2330-7175dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42809414 | ||||||
chr10:42809423 | T | C | 1 | a0001c0003t0001g0249 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2330-7176T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42809423 | |||||||
chr10:42809809 | A | G | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2330-6790A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42809809 | |||||||
chr10:42809952 | AT | A | 49 | a0001c0003t0001g0018 a0001c0004t0003g0007 a0001c0004t0003g0021 others(46): Show |
57 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2330-6625delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42809952 | ||||||
chr10:42809952 | ATT | A | 109 | a0001c0004t0003g0072 a0001c0004t0018g0044 a0001c0004t0018g0045 others(106): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2330-6626_2330-662 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42809952 | ||||||
chr10:42809993 | G | C | 1 | a0001c0013t0008g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2330-6606G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42809993 | |||||||
chr10:42810010 | C | G | 1 | a0001c0004t0003g0151 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2330-6589C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810010 | |||||||
chr10:42810032 | G | A | 1 | a0001c0004t0033g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2330-6567G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810032 | |||||||
chr10:42810150 | C | T | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2330-6449C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810150 | |||||||
chr10:42810198 | GTGT | G | 60 | a0002c0001t0001g0004 a0002c0001t0001g0005 a0002c0001t0001g0008 others(57): Show |
86 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.2330-6399_2330-639 others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42810198 | ||||||
chr10:42810212 | T | C | 47 | a0003c0002t0002g0001 a0003c0002t0002g0010 a0003c0002t0002g0022 others(44): Show |
76 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2330-6387T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810212 | |||||||
chr10:42810273 | C | T | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2330-6326C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810273 | |||||||
chr10:42810470 | T | G | 166 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(163): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2330-6129T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810470 | |||||||
chr10:42810501 | G | C | 1 | a0003c0002t0002g0105 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2330-6098G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810501 | |||||||
chr10:42810688 | C | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2330-5911C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810688 | |||||||
chr10:42810743 | G | A | 6 | a0001c0004t0028g0049 a0001c0008t0007g0014 a0001c0008t0007g0154 others(3): Show |
8 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2330-5856G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810743 | |||||||
chr10:42810886 | T | G | 1 | a0002c0001t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2330-5713T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42810886 | |||||||
chr10:42811049 | AT | A | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-5540delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42811049 | ||||||
chr10:42811052 | T | A | 1 | a0001c0003t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2330-5547T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811052 | |||||||
chr10:42811071 | T | C | 1 | a0003c0002t0002g0092 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2330-5528T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811071 | |||||||
chr10:42811323 | A | G | 164 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(161): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.2330-5276A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811323 | |||||||
chr10:42811332 | C | G | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2330-5267C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811332 | |||||||
chr10:42811334 | C | T | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2330-5265C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811334 | |||||||
chr10:42811506 | A | G | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2330-5093A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811506 | |||||||
chr10:42811520 | C | CT | 8 | a0003c0002t0002g0092 a0003c0002t0002g0107 a0003c0025t0002g0142 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.2330-5074dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42811520 | ||||||
chr10:42811520 | C | CTT | 69 | a0001c0004t0003g0066 a0001c0004t0011g0048 a0001c0004t0033g0143 others(66): Show |
107 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2330-5075_2330-507 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42811520 | ||||||
chr10:42811520 | C | CTTT | 61 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(58): Show |
74 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.2330-5076_2330-507 others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42811520 | ||||||
chr10:42811520 | C | CTTTT | 10 | a0001c0004t0003g0054 a0001c0004t0003g0073 a0001c0004t0003g0077 others(7): Show |
10 | HG01123.hp1 HG01891.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.2330-5077_2330-507 others(8): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42811520 | ||||||
chr10:42811525 | TC | T | 6 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.2330-5073delC | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811525 | |||||||
chr10:42811526 | C | T | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2330-5073C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811526 | |||||||
chr10:42811549 | G | A | 1 | a0002c0001t0001g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2330-5050G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811549 | |||||||
chr10:42811617 | T | C | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-4982T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811617 | |||||||
chr10:42811682 | G | A | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2330-4917G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811682 | |||||||
chr10:42811759 | C | G | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2330-4840C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811759 | |||||||
chr10:42811760 | G | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2330-4839G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811760 | |||||||
chr10:42811766 | C | T | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2330-4833C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42811766 | |||||||
chr10:42812020 | T | C | 2 | a0003c0002t0002g0111 a0021c0022t0002g0094 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2330-4579T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812020 | |||||||
chr10:42812445 | C | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2330-4154C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812445 | |||||||
chr10:42812470 | G | A | 1 | a0001c0004t0003g0053 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2330-4129G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812470 | |||||||
chr10:42812472 | G | A | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-4127G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812472 | |||||||
chr10:42812482 | A | G | 1 | a0001c0004t0003g0053 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2330-4117A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812482 | |||||||
chr10:42812530 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2330-4069G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812530 | |||||||
chr10:42812610 | G | A | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2330-3989G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812610 | |||||||
chr10:42812610 | G | T | 2 | a0003c0002t0002g0115 a0003c0031t0002g0116 |
2 | HG00558.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2330-3989G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812610 | |||||||
chr10:42812765 | C | T | 1 | a0003c0002t0002g0101 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2330-3834C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812765 | |||||||
chr10:42812927 | G | T | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2330-3672G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812927 | |||||||
chr10:42812931 | G | A | 1 | a0001c0005t0025g0133 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2330-3668G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42812931 | |||||||
chr10:42813035 | C | T | 1 | a0001c0005t0004g0127 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2330-3564C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813035 | |||||||
chr10:42813261 | G | T | 3 | a0001c0004t0003g0053 a0001c0004t0003g0063 a0001c0004t0003g0064 |
3 | HG02683.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2330-3338G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813261 | |||||||
chr10:42813539 | G | C | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2330-3060G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813539 | |||||||
chr10:42813598 | G | A | 1 | a0001c0003t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2330-3001G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813598 | |||||||
chr10:42813625 | G | A | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2330-2974G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813625 | |||||||
chr10:42813768 | C | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2330-2831C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813768 | |||||||
chr10:42813806 | C | G | 15 | a0002c0001t0001g0037 a0002c0001t0001g0039 a0002c0001t0001g0239 others(12): Show |
17 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2330-2793C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813806 | |||||||
chr10:42813826 | T | A | 1 | a0006c0009t0002g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2330-2773T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813826 | |||||||
chr10:42813987 | C | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2330-2612C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42813987 | |||||||
chr10:42814068 | G | A | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2330-2531G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814068 | |||||||
chr10:42814147 | A | G | 1 | a0001c0003t0001g0197 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2330-2452A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814147 | |||||||
chr10:42814183 | C | T | 2 | a0005c0007t0001g0195 a0005c0007t0001g0196 |
2 | NA18952.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2330-2416C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814183 | |||||||
chr10:42814360 | G | A | 1 | a0003c0002t0002g0103 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2330-2239G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814360 | |||||||
chr10:42814380 | G | C | 1 | a0001c0005t0004g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2330-2219G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814380 | |||||||
chr10:42814396 | A | AT | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.2330-2194dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr10 | 42814396 | ||||||
chr10:42814525 | T | G | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2330-2074T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814525 | |||||||
chr10:42814586 | T | C | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2330-2013T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814586 | |||||||
chr10:42814593 | T | G | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2330-2006T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814593 | |||||||
chr10:42814614 | T | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-1985T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814614 | |||||||
chr10:42814628 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-1971A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814628 | |||||||
chr10:42814818 | G | A | 33 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(30): Show |
40 | HG01928.hp2 HG01943.hp2 HG01978.hp1 others(37): Show |
intron_variant | MODIFIER | c.2330-1781G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814818 | |||||||
chr10:42814824 | G | A | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2330-1775G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814824 | |||||||
chr10:42814857 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-1742A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814857 | |||||||
chr10:42814918 | C | T | 2 | a0003c0002t0002g0010 a0003c0002t0002g0104 |
5 | HG00642.hp2 HG03017.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2330-1681C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42814918 | |||||||
chr10:42815155 | G | A | 1 | a0002c0001t0001g0219 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2330-1444G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815155 | |||||||
chr10:42815165 | G | A | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.2330-1434G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815165 | |||||||
chr10:42815295 | G | A | 2 | a0008c0016t0013g0046 a0008c0016t0013g0047 |
2 | HG01978.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2330-1304G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815295 | |||||||
chr10:42815488 | T | C | 2 | a0003c0002t0002g0089 a0003c0002t0002g0096 |
2 | HG00621.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2330-1111T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815488 | |||||||
chr10:42815941 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-658A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815941 | |||||||
chr10:42815966 | A | G | 1 | a0001c0003t0006g0201 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2330-633A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42815966 | |||||||
chr10:42816041 | G | C | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2330-558G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816041 | |||||||
chr10:42816100 | G | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2330-499G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816100 | |||||||
chr10:42816173 | C | T | 1 | a0002c0001t0001g0226 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2330-426C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816173 | |||||||
chr10:42816311 | A | G | 1 | a0005c0007t0001g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2330-288A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816311 | |||||||
chr10:42816328 | T | G | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2330-271T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816328 | |||||||
chr10:42816340 | A | G | 1 | a0001c0004t0003g0056 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2330-259A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816340 | |||||||
chr10:42816379 | G | A | 1 | a0001c0008t0007g0155 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2330-220G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816379 | |||||||
chr10:42816388 | A | C | 1 | a0002c0001t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2330-211A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816388 | |||||||
chr10:42816530 | G | C | 1 | a0002c0001t0001g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2330-69G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816530 | |||||||
chr10:42816547 | C | T | 1 | a0001c0004t0003g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2330-52C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816547 | |||||||
chr10:42816556 | C | T | 2 | a0002c0001t0017g0242 a0002c0001t0017g0243 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2330-43C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 13/22 | chr10 | 42816556 | |||||||
chr10:42816730 | T | C | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2403+58T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42816730 | |||||||
chr10:42816757 | G | A | 1 | a0022c0033t0001g0230 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2403+85G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42816757 | |||||||
chr10:42816779 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2403+107A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42816779 | |||||||
chr10:42816915 | C | T | 1 | a0005c0007t0001g0189 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2403+243C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42816915 | |||||||
chr10:42816965 | T | C | 41 | a0001c0003t0001g0200 a0002c0001t0001g0004 a0002c0001t0001g0005 others(38): Show |
65 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.2403+293T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42816965 | |||||||
chr10:42817006 | G | A | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2404-312G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 14/22 | chr10 | 42817006 | |||||||
chr10:42817522 | C | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2580+28C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817522 | |||||||
chr10:42817543 | C | T | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2580+49C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817543 | |||||||
chr10:42817548 | G | T | 1 | a0001c0004t0003g0021 | 2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2580+54G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817548 | |||||||
chr10:42817619 | C | T | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2580+125C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817619 | |||||||
chr10:42817648 | G | T | 1 | a0001c0003t0001g0234 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2580+154G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817648 | |||||||
chr10:42817684 | T | C | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2580+190T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817684 | |||||||
chr10:42817842 | A | G | 1 | a0004c0006t0005g0167 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2580+348A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42817842 | |||||||
chr10:42818001 | T | C | 1 | a0001c0008t0008g0027 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2580+507T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818001 | |||||||
chr10:42818076 | C | T | 12 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2580+582C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818076 | |||||||
chr10:42818108 | G | T | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2580+614G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818108 | |||||||
chr10:42818359 | G | A | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2580+865G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818359 | |||||||
chr10:42818437 | C | T | 2 | a0001c0004t0003g0060 a0001c0004t0003g0061 |
2 | HG01070.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2580+943C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818437 | |||||||
chr10:42818491 | G | A | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2580+997G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818491 | |||||||
chr10:42818660 | G | A | 1 | a0004c0006t0005g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2580+1166G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818660 | |||||||
chr10:42818772 | G | A | 1 | a0003c0002t0002g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2580+1278G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818772 | |||||||
chr10:42818812 | T | C | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2580+1318T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818812 | |||||||
chr10:42818889 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2581-1347A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818889 | |||||||
chr10:42818979 | G | A | 1 | a0001c0003t0009g0035 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2581-1257G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818979 | |||||||
chr10:42818982 | C | G | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2581-1254C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818982 | |||||||
chr10:42818989 | G | A | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2581-1247G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42818989 | |||||||
chr10:42819048 | C | T | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2581-1188C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819048 | |||||||
chr10:42819068 | A | G | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2581-1168A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819068 | |||||||
chr10:42819084 | G | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.2581-1152G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819084 | |||||||
chr10:42819112 | G | C | 1 | a0003c0002t0002g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2581-1124G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819112 | |||||||
chr10:42819242 | C | T | 15 | a0002c0001t0001g0037 a0002c0001t0001g0039 a0002c0001t0001g0239 others(12): Show |
17 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2581-994C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819242 | |||||||
chr10:42819274 | C | T | 1 | a0001c0004t0003g0053 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2581-962C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819274 | |||||||
chr10:42819289 | G | T | 1 | a0015c0035t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2581-947G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819289 | |||||||
chr10:42819295 | TC | T | 3 | a0002c0001t0001g0248 a0002c0001t0017g0242 a0002c0001t0017g0243 |
3 | HG01167.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2581-940delC | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819295 | |||||||
chr10:42819435 | A | G | 1 | a0015c0035t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2581-801A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819435 | |||||||
chr10:42819649 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2581-587A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819649 | |||||||
chr10:42819695 | A | G | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.2581-541A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819695 | |||||||
chr10:42819695 | A | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2581-541A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819695 | |||||||
chr10:42819896 | A | G | 1 | a0002c0001t0001g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2581-340A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819896 | |||||||
chr10:42819901 | C | G | 1 | a0001c0004t0003g0061 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2581-335C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819901 | |||||||
chr10:42819980 | C | T | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2581-256C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42819980 | |||||||
chr10:42820041 | C | G | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2581-195C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 15/22 | chr10 | 42820041 | |||||||
chr10:42820473 | C | G | 1 | a0011c0017t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2770-35C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 16/22 | chr10 | 42820473 | |||||||
chr10:42820722 | A | G | 165 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(162): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2950+34A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/22 | chr10 | 42820722 | |||||||
chr10:42820724 | G | A | 1 | a0002c0001t0001g0220 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2950+36G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/22 | chr10 | 42820724 | |||||||
chr10:42820735 | A | G | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2950+47A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/22 | chr10 | 42820735 | |||||||
chr10:42820824 | G | A | 1 | a0001c0004t0028g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2951-110G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/22 | chr10 | 42820824 | |||||||
chr10:42820915 | T | C | 2 | a0004c0006t0005g0174 a0004c0006t0031g0168 |
2 | NA19063.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2951-19T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 17/22 | chr10 | 42820915 | |||||||
chr10:42821539 | C | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.3010-523C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | chr10 | 42821539 | |||||||
chr10:42821542 | C | CT | 48 | a0001c0004t0003g0021 a0001c0004t0003g0026 a0001c0004t0003g0066 others(45): Show |
60 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.3010-492dupT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821542 | C | CTT | 22 | a0001c0004t0003g0007 a0001c0004t0003g0056 a0001c0004t0003g0057 others(19): Show |
27 | HG01070.hp1 HG01081.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.3010-493_3010-492d others(4): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821542 | C | CTTT | 10 | a0001c0004t0003g0050 a0001c0004t0003g0054 a0001c0004t0003g0055 others(7): Show |
10 | HG01934.hp1 HG02145.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.3010-494_3010-492d others(5): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821542 | CT | C | 83 | a0001c0003t0001g0002 a0001c0003t0001g0006 a0001c0003t0001g0016 others(80): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.3010-492delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821542 | CTTT | C | 5 | a0001c0008t0007g0014 a0001c0008t0007g0155 a0001c0008t0007g0157 others(2): Show |
7 | HG00099.hp1 HG01516.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.3010-494_3010-492d others(5): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821542 | CTTTTTTT others(3): Show |
C | 3 | a0001c0005t0004g0132 a0001c0005t0004g0135 a0001c0005t0004g0137 |
3 | HG02647.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3010-501_3010-492d others(12): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr10 | 42821542 | ||||||
chr10:42821601 | G | A | 1 | a0003c0002t0002g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3010-461G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | chr10 | 42821601 | |||||||
chr10:42821655 | C | T | 1 | a0015c0035t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3010-407C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | chr10 | 42821655 | |||||||
chr10:42821814 | A | G | 2 | a0001c0004t0018g0044 a0001c0004t0018g0045 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3010-248A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | chr10 | 42821814 | |||||||
chr10:42822051 | G | A | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.3010-11G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 18/22 | chr10 | 42822051 | |||||||
chr10:42822278 | T | G | 247 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(244): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.3132+94T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | chr10 | 42822278 | |||||||
chr10:42822332 | C | A | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.3132+148C>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | chr10 | 42822332 | |||||||
chr10:42822406 | TC | T | 4 | a0001c0026t0013g0260 a0001c0030t0032g0043 a0008c0016t0013g0046 others(1): Show |
4 | HG01978.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3132+224delC | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr10 | 42822406 | ||||||
chr10:42822740 | C | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3133-378C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | chr10 | 42822740 | |||||||
chr10:42822763 | T | C | 29 | a0001c0005t0004g0011 a0001c0005t0004g0012 a0001c0005t0004g0013 others(26): Show |
36 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.3133-355T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | chr10 | 42822763 | |||||||
chr10:42822774 | G | T | 2 | a0001c0004t0003g0059 a0001c0004t0003g0075 |
2 | HG02273.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3133-344G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 19/22 | chr10 | 42822774 | |||||||
chr10:42823296 | G | A | 1 | a0003c0002t0002g0099 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3280+31G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823296 | |||||||
chr10:42823306 | T | A | 1 | a0003c0002t0002g0105 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3280+41T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823306 | |||||||
chr10:42823316 | C | G | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3280+51C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823316 | |||||||
chr10:42823329 | T | G | 1 | a0001c0004t0003g0053 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3280+64T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823329 | |||||||
chr10:42823498 | C | T | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-111C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823498 | |||||||
chr10:42823559 | G | T | 1 | a0001c0005t0004g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3281-50G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823559 | |||||||
chr10:42823606 | C | T | 2 | a0005c0007t0001g0029 a0005c0007t0001g0193 |
3 | HG00673.hp2 NA18984.hp1 NA18998.hp1 |
splice_region_variant&intron_variant | LOW | c.3281-3C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 20/22 | chr10 | 42823606 | |||||||
chr10:42823807 | T | C | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3456+23T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42823807 | |||||||
chr10:42823838 | A | C | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3456+54A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42823838 | |||||||
chr10:42823898 | A | G | 1 | a0003c0002t0002g0001 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3456+114A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42823898 | |||||||
chr10:42823901 | G | A | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3456+117G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42823901 | |||||||
chr10:42824059 | A | G | 1 | a0001c0013t0008g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3456+275A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824059 | |||||||
chr10:42824534 | C | T | 4 | a0001c0026t0013g0260 a0001c0030t0032g0043 a0008c0016t0013g0046 others(1): Show |
4 | HG01978.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3456+750C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824534 | |||||||
chr10:42824557 | A | G | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3456+773A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824557 | |||||||
chr10:42824586 | G | C | 1 | a0001c0005t0004g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3456+802G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824586 | |||||||
chr10:42824686 | A | G | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.3456+902A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824686 | |||||||
chr10:42824710 | T | C | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.3456+926T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824710 | |||||||
chr10:42824801 | T | C | 2 | a0008c0016t0013g0046 a0008c0016t0013g0047 |
2 | HG01978.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3456+1017T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42824801 | |||||||
chr10:42825282 | C | G | 1 | a0001c0030t0032g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3456+1498C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825282 | |||||||
chr10:42825299 | G | A | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3456+1515G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825299 | |||||||
chr10:42825312 | T | G | 1 | a0001c0003t0001g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3456+1528T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825312 | |||||||
chr10:42825374 | A | G | 1 | a0002c0001t0001g0211 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3456+1590A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825374 | |||||||
chr10:42825411 | T | G | 1 | a0001c0005t0004g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3456+1627T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825411 | |||||||
chr10:42825502 | A | G | 1 | a0002c0001t0001g0223 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3456+1718A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825502 | |||||||
chr10:42825510 | CCTT | C | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3456+1730_3456+173 others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42825510 | ||||||
chr10:42825552 | C | T | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3456+1768C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825552 | |||||||
chr10:42825693 | T | A | 17 | a0001c0005t0004g0012 a0001c0005t0004g0013 a0001c0005t0004g0117 others(14): Show |
20 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.3456+1909T>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825693 | |||||||
chr10:42825774 | T | C | 1 | a0001c0004t0003g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3456+1990T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825774 | |||||||
chr10:42825945 | A | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.3456+2161A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825945 | |||||||
chr10:42825969 | A | G | 2 | a0001c0004t0003g0150 a0001c0004t0003g0151 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3456+2185A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42825969 | |||||||
chr10:42826119 | C | T | 1 | a0002c0001t0001g0222 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3456+2335C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826119 | |||||||
chr10:42826191 | A | G | 1 | a0026c0020t0008g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3456+2407A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826191 | |||||||
chr10:42826216 | T | C | 1 | a0005c0007t0001g0192 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3456+2432T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826216 | |||||||
chr10:42826237 | T | TTG | 15 | a0001c0004t0011g0048 a0001c0005t0004g0011 a0001c0005t0004g0024 others(12): Show |
16 | HG00741.hp1 HG01109.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.3456+2495_3456+249 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | T | TTGTG | 6 | a0001c0005t0004g0130 a0001c0005t0004g0137 a0001c0005t0004g0140 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.3456+2493_3456+249 others(8): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | T | TTGTGTGT others(1): Show |
4 | a0001c0008t0007g0154 a0001c0008t0015g0159 a0001c0008t0019g0156 others(1): Show |
4 | HG00140.hp1 HG02280.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3456+2489_3456+249 others(12): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | T | TTGTGTGT others(3): Show |
2 | a0001c0008t0007g0014 a0001c0008t0007g0155 |
3 | HG00099.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.3456+2487_3456+249 others(14): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | T | TTGTGTGT others(5): Show |
1 | a0001c0008t0015g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3456+2485_3456+249 others(16): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTG | T | 83 | a0001c0003t0001g0002 a0001c0003t0001g0006 a0001c0003t0001g0016 others(80): Show |
117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.3456+2495_3456+249 others(6): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTG | T | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0232 others(9): Show |
12 | HG00642.hp1 HG02055.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.3456+2493_3456+249 others(8): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTGTG | T | 23 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0033 others(20): Show |
29 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.3456+2491_3456+249 others(10): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTGTGT others(1): Show |
T | 78 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(75): Show |
111 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.3456+2489_3456+249 others(12): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTGTGT others(3): Show |
T | 25 | a0001c0004t0029g0078 a0003c0002t0002g0114 a0004c0006t0005g0003 others(22): Show |
34 | HG00544.hp2 HG00609.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.3456+2487_3456+249 others(14): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTGTGT others(5): Show |
T | 3 | a0003c0002t0002g0104 a0012c0015t0003g0051 a0012c0015t0003g0052 |
3 | HG00642.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3456+2485_3456+249 others(16): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826237 | TTGTGTGT others(7): Show |
T | 1 | a0001c0005t0004g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3456+2483_3456+249 others(18): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826237 | ||||||
chr10:42826246 | T | G | 2 | a0003c0002t0002g0115 a0003c0031t0002g0116 |
2 | HG00558.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3456+2462T>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826246 | |||||||
chr10:42826253 | G | T | 2 | a0003c0002t0002g0115 a0003c0031t0002g0116 |
2 | HG00558.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3456+2469G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826253 | |||||||
chr10:42826279 | GT | G | 3 | a0001c0003t0001g0202 a0005c0007t0001g0029 a0013c0018t0004g0139 |
3 | HG04115.hp1 NA18984.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.3456+2499delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42826279 | ||||||
chr10:42826538 | G | A | 4 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(1): Show |
6 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3456+2754G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826538 | |||||||
chr10:42826562 | T | C | 1 | a0001c0003t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3456+2778T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826562 | |||||||
chr10:42826699 | G | A | 2 | a0001c0003t0009g0034 a0001c0003t0009g0035 |
4 | HG01168.hp1 HG01169.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3456+2915G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826699 | |||||||
chr10:42826722 | C | G | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3456+2938C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826722 | |||||||
chr10:42826877 | C | T | 153 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(150): Show |
204 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3456+3093C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826877 | |||||||
chr10:42826932 | C | T | 2 | a0004c0006t0005g0161 a0023c0024t0005g0171 |
2 | NA18747.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3456+3148C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42826932 | |||||||
chr10:42827069 | G | T | 1 | a0003c0002t0002g0105 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3457-3192G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827069 | |||||||
chr10:42827074 | G | A | 1 | a0002c0001t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3457-3187G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827074 | |||||||
chr10:42827138 | G | A | 1 | a0003c0002t0002g0090 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3457-3123G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827138 | |||||||
chr10:42827153 | G | A | 1 | a0006c0009t0002g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3457-3108G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827153 | |||||||
chr10:42827275 | A | C | 1 | a0001c0004t0029g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3457-2986A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827275 | |||||||
chr10:42827284 | G | A | 1 | a0003c0002t0002g0141 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3457-2977G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827284 | |||||||
chr10:42827321 | G | A | 1 | a0001c0005t0004g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3457-2940G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827321 | |||||||
chr10:42827343 | G | A | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3457-2918G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827343 | |||||||
chr10:42827515 | C | T | 1 | a0001c0003t0006g0030 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3457-2746C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827515 | |||||||
chr10:42827539 | G | C | 1 | a0001c0003t0006g0201 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3457-2722G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827539 | |||||||
chr10:42827827 | G | A | 1 | a0004c0006t0005g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3457-2434G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827827 | |||||||
chr10:42827848 | C | G | 1 | a0001c0005t0004g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3457-2413C>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42827848 | |||||||
chr10:42828109 | C | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3457-2152C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828109 | |||||||
chr10:42828110 | G | A | 3 | a0001c0005t0004g0138 a0002c0001t0001g0210 a0002c0001t0001g0212 |
3 | HG03041.hp2 NA18942.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3457-2151G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828110 | |||||||
chr10:42828187 | C | T | 2 | a0001c0008t0015g0158 a0001c0008t0015g0159 |
2 | HG00735.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3457-2074C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828187 | |||||||
chr10:42828326 | G | T | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3457-1935G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828326 | |||||||
chr10:42828546 | TCCA | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.3457-1708_3457-170 others(7): Show |
BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42828546 | ||||||
chr10:42828552 | A | G | 15 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0038 others(12): Show |
24 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.3457-1709A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828552 | |||||||
chr10:42828613 | GT | G | 26 | a0004c0006t0005g0003 a0004c0006t0005g0015 a0004c0006t0005g0160 others(23): Show |
35 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.3457-1635delT | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42828613 | ||||||
chr10:42828773 | G | A | 19 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0036 others(16): Show |
28 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3457-1488G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828773 | |||||||
chr10:42828779 | G | A | 1 | a0001c0005t0026g0125 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3457-1482G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828779 | |||||||
chr10:42828884 | A | T | 2 | a0010c0012t0014g0261 a0010c0012t0014g0262 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3457-1377A>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42828884 | |||||||
chr10:42829033 | G | C | 46 | a0003c0002t0002g0001 a0003c0002t0002g0010 a0003c0002t0002g0022 others(43): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3457-1228G>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829033 | |||||||
chr10:42829114 | G | T | 3 | a0001c0004t0011g0048 a0007c0014t0011g0040 a0007c0014t0011g0041 |
3 | HG01109.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3457-1147G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829114 | |||||||
chr10:42829185 | G | A | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3457-1076G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829185 | |||||||
chr10:42829297 | C | T | 46 | a0003c0002t0002g0001 a0003c0002t0002g0010 a0003c0002t0002g0022 others(43): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3457-964C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829297 | |||||||
chr10:42829322 | A | C | 10 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(7): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3457-939A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829322 | |||||||
chr10:42829407 | G | A | 1 | a0002c0001t0001g0221 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3457-854G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829407 | |||||||
chr10:42829763 | A | C | 1 | a0003c0025t0002g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3457-498A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829763 | |||||||
chr10:42829770 | G | A | 2 | a0003c0002t0002g0108 a0004c0006t0005g0169 |
2 | NA18942.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3457-491G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829770 | |||||||
chr10:42829838 | CA | C | 159 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(156): Show |
212 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.3457-415delA | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr10 | 42829838 | ||||||
chr10:42829882 | G | A | 1 | a0001c0003t0001g0234 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3457-379G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42829882 | |||||||
chr10:42830027 | G | T | 5 | a0002c0001t0001g0005 a0002c0001t0001g0185 a0002c0001t0001g0205 others(2): Show |
5 | HG01261.hp1 HG01358.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.3457-234G>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42830027 | |||||||
chr10:42830110 | A | C | 1 | a0010c0012t0014g0262 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3457-151A>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42830110 | |||||||
chr10:42830145 | C | T | 39 | a0001c0004t0003g0007 a0001c0004t0003g0021 a0001c0004t0003g0026 others(36): Show |
45 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.3457-116C>T | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42830145 | |||||||
chr10:42830158 | A | G | 167 | a0001c0003t0001g0198 a0001c0004t0003g0007 a0001c0004t0003g0021 others(164): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.3457-103A>G | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42830158 | |||||||
chr10:42830216 | T | C | 5 | a0001c0008t0007g0014 a0001c0008t0007g0154 a0001c0008t0007g0155 others(2): Show |
7 | HG00099.hp1 HG00140.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.3457-45T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 21/22 | chr10 | 42830216 | |||||||
chr10:42830497 | T | C | 1 | a0003c0027t0002g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3618+75T>C | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 22/22 | chr10 | 42830497 | |||||||
chr10:42830779 | G | A | 17 | a0001c0005t0004g0012 a0001c0005t0004g0013 a0001c0005t0004g0117 others(14): Show |
20 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.3619-87G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 22/22 | chr10 | 42830779 | |||||||
chr10:42830848 | G | A | 2 | a0004c0006t0005g0161 a0023c0024t0005g0171 |
2 | NA18747.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3619-18G>A | BMS1 | ENSG00000165733.8 | transcript | ENST00000374518.6 | protein_coding | 22/22 | chr10 | 42830848 |