Item | Value |
---|---|
geneid | 57082 |
ensemblid | ENSG00000137812.21 |
hgncid | 24054 |
symbol | KNL1 |
name | kinetochore scaffold 1 |
refseq_nuc | NM_144508.5 |
refseq_prot | NP_653091.3 |
ensembl_nuc | ENST00000399668.7 |
ensembl_prot | ENSP00000382576.3 |
mane_status | MANE Select |
chr | chr15 |
start | 40594249 |
end | 40664342 |
strand | + |
ver | v1.2 |
region | chr15:40594249-40664342 |
region5000 | chr15:40589249-40669342 |
regionname0 | KNL1_chr15_40594249_40664342 |
regionname5000 | KNL1_chr15_40589249_40669342 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2316 | 119 | 4 | 20 | 75 | 6 | 13 | 57 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0002 | 0/1 | 2316 | 99 | 8 | 18 | 52 | 2 | 18 | 40 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0003 | 0/0 | 2316 | 48 | 2 | 15 | 18 | 3 | 10 | 9 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0004 | 0/0 | 2316 | 27 | 26 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0005 | 0/0 | 2316 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0006 | 0/0 | 2316 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0007 | 0/0 | 2316 | 7 | 0 | 6 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0008 | 0/0 | 2316 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0009 | 0/0 | 2316 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0010 | 0/0 | 2316 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0011 | 0/0 | 2316 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0012 | 0/0 | 2316 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0013 | 0/0 | 2316 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0014 | 0/0 | 2316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0015 | 0/0 | 2316 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0016 | 0/0 | 2316 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0017 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0018 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0019 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0020 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0021 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0022 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0023 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0024 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0025 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0026 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0027 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0028 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0029 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0030 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0031 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0032 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
a0033 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | MDGVS others(2311): Show |
chr15 | 40589249 | 40669342 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6948 | 102 | 4 | 19 | 59 | 6 | 13 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0001c0006 | 0/0 | 6948 | 15 | 0 | 1 | 14 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0001c0038 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0001c0039 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0002c0002 | 0/1 | 6948 | 95 | 6 | 18 | 51 | 2 | 17 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0002c0022 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0002c0024 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0002c0025 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0002c0028 | 0/0 | 6948 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0003c0003 | 0/0 | 6948 | 48 | 2 | 15 | 18 | 3 | 10 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0004c0004 | 0/0 | 6948 | 23 | 22 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0004c0011 | 0/0 | 6948 | 4 | 4 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0005c0005 | 0/0 | 6948 | 16 | 15 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0005c0015 | 0/0 | 6948 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0006c0007 | 0/0 | 6948 | 9 | 9 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0007c0008 | 0/0 | 6948 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0008c0009 | 0/0 | 6948 | 4 | 3 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0009c0010 | 0/0 | 6948 | 4 | 0 | 0 | 4 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0010c0013 | 0/0 | 6948 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0011c0012 | 0/0 | 6948 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0012c0014 | 0/0 | 6948 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0013c0016 | 0/0 | 6948 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0014c0018 | 0/0 | 6948 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0015c0017 | 0/0 | 6948 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0016c0019 | 0/0 | 6948 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0017c0034 | 0/0 | 6948 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0018c0030 | 0/0 | 6948 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0019c0037 | 0/0 | 6948 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0020c0041 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0021c0021 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0022c0029 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0023c0020 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0024c0033 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0025c0040 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0026c0026 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0027c0036 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0028c0032 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0029c0035 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0030c0027 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0031c0031 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0032c0023 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 | ||
a0033c0042 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | ATGGA others(6943): Show |
chr15 | 40589249 | 40669342 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9266 | 88 | 4 | 6 | 59 | 6 | 12 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0001c0001t0004 | 0/0 | 9266 | 13 | 0 | 13 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0001c0001t0012 | 0/0 | 9320 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9315): Show |
chr15 | 40589249 | 40669342 |
a0001c0006t0001 | 0/0 | 9266 | 15 | 0 | 1 | 14 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0001c0038t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0001c0039t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0002t0001 | 0/1 | 9266 | 35 | 5 | 3 | 20 | 0 | 6 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0002t0003 | 0/0 | 9266 | 58 | 1 | 15 | 29 | 2 | 11 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0002t0008 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0002t0016 | 0/0 | 9206 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9201): Show |
chr15 | 40589249 | 40669342 |
a0002c0022t0015 | 0/0 | 9311 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9306): Show |
chr15 | 40589249 | 40669342 |
a0002c0024t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0025t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0002c0028t0003 | 0/0 | 9266 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0003c0003t0002 | 0/0 | 9266 | 45 | 2 | 15 | 16 | 3 | 9 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0003c0003t0010 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0003c0003t0011 | 0/0 | 9266 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0003c0003t0014 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0004c0004t0001 | 0/0 | 9266 | 23 | 22 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0004c0011t0001 | 0/0 | 9266 | 4 | 4 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0005c0005t0002 | 0/0 | 9266 | 16 | 15 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0005c0015t0002 | 0/0 | 9266 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0006c0007t0001 | 0/0 | 9266 | 9 | 9 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0007c0008t0005 | 0/0 | 9266 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0008c0009t0006 | 0/0 | 9266 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0008c0009t0007 | 0/0 | 9266 | 2 | 1 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0009c0010t0001 | 0/0 | 9266 | 4 | 0 | 0 | 4 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0010c0013t0001 | 0/0 | 9266 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0011c0012t0001 | 0/0 | 9266 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0012c0014t0001 | 0/0 | 9266 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0013c0016t0003 | 0/0 | 9266 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0014c0018t0002 | 0/0 | 9266 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0015c0017t0003 | 0/0 | 9266 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0016c0019t0003 | 0/0 | 9266 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0017c0034t0013 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0018c0030t0002 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0019c0037t0001 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0020c0041t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0021c0021t0002 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0022c0029t0009 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0023c0020t0002 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0024c0033t0017 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0025c0040t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0026c0026t0003 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0027c0036t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0028c0032t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0029c0035t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0030c0027t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0031c0031t0002 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0032c0023t0006 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
a0033c0042t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | AGATT others(9261): Show |
chr15 | 40589249 | 40669342 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0348 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0006t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0038t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0001c0039t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0002t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0022t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0024t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0025t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0002c0028t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0011g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0003c0003t0014g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0004t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0011t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0011t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0011t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0004c0011t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0005t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0015t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0015t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0005c0015t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0006c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0007c0008t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0008c0009t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0008c0009t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0008c0009t0007g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0008c0009t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0009c0010t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0009c0010t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0009c0010t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0009c0010t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0010c0013t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0010c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0010c0013t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0011c0012t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0011c0012t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0011c0012t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0012c0014t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0012c0014t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0012c0014t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0013c0016t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0013c0016t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0014c0018t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0014c0018t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0015c0017t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0015c0017t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0016c0019t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0016c0019t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0017c0034t0013g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0018c0030t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0019c0037t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0020c0041t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0021c0021t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0022c0029t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0023c0020t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0024c0033t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0025c0040t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0026c0026t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0027c0036t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0028c0032t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0029c0035t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0030c0027t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0031c0031t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0032c0023t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
a0033c0042t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0002 | g0169 | EUR | GBR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00099 | hp2 | a0002 | c0002 | t0003 | g0042 | EUR | GBR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0353 | EUR | FIN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0181 | EUR | FIN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00408 | hp2 | a0003 | c0003 | t0002 | g0195 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00544 | hp1 | a0001 | c0039 | t0001 | g0347 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00544 | hp2 | a0013 | c0016 | t0003 | g0036 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0174 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00558 | hp2 | a0001 | c0006 | t0001 | g0228 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00597 | hp2 | a0010 | c0013 | t0001 | g0101 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00609 | hp1 | a0003 | c0003 | t0002 | g0158 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00609 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00639 | hp1 | a0002 | c0002 | t0003 | g0130 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0186 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00642 | hp1 | a0007 | c0008 | t0005 | g0038 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00642 | hp2 | a0004 | c0004 | t0001 | g0260 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00673 | hp2 | a0001 | c0006 | t0001 | g0226 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0156 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00738 | hp1 | a0007 | c0008 | t0005 | g0002 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00738 | hp2 | a0003 | c0003 | t0002 | g0361 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00741 | hp1 | a0017 | c0034 | t0013 | g0015 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0071 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01069 | hp2 | a0007 | c0008 | t0005 | g0054 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0362 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0363 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01071 | hp2 | a0007 | c0008 | t0005 | g0002 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0359 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01081 | hp2 | a0007 | c0008 | t0005 | g0081 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01106 | hp2 | a0002 | c0002 | t0003 | g0050 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0316 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01109 | hp2 | a0008 | c0009 | t0007 | g0007 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0185 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0155 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0313 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0084 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01255 | hp1 | a0005 | c0005 | t0002 | g0166 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01255 | hp2 | a0007 | c0008 | t0005 | g0076 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01256 | hp1 | a0003 | c0003 | t0002 | g0157 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01256 | hp2 | a0019 | c0037 | t0001 | g0268 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0182 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0322 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01358 | hp2 | a0003 | c0003 | t0002 | g0360 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01361 | hp1 | a0003 | c0003 | t0002 | g0202 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0069 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01515 | hp2 | a0007 | c0008 | t0005 | g0053 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01516 | hp2 | a0003 | c0003 | t0002 | g0172 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0199 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01891 | hp2 | a0004 | c0004 | t0001 | g0244 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0056 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01928 | hp2 | a0001 | c0006 | t0001 | g0235 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01952 | hp1 | a0002 | c0002 | t0003 | g0077 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01975 | hp1 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01978 | hp2 | a0003 | c0003 | t0002 | g0194 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01981 | hp1 | a0003 | c0003 | t0002 | g0147 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01993 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02015 | hp2 | a0003 | c0003 | t0002 | g0187 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02027 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02040 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02055 | hp1 | a0004 | c0004 | t0001 | g0253 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02055 | hp2 | a0014 | c0018 | t0002 | g0203 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02056 | hp2 | a0003 | c0003 | t0014 | g0188 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02080 | hp1 | a0001 | c0006 | t0001 | g0224 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02083 | hp2 | a0020 | c0041 | t0001 | g0218 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02132 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02132 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02135 | hp2 | a0003 | c0003 | t0002 | g0149 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02145 | hp1 | a0021 | c0021 | t0002 | g0207 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02145 | hp2 | a0004 | c0011 | t0001 | g0239 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0037 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02165 | hp2 | a0003 | c0003 | t0002 | g0173 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02257 | hp1 | a0022 | c0029 | t0009 | g0191 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02257 | hp2 | a0004 | c0011 | t0001 | g0238 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0289 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0057 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02280 | hp1 | a0023 | c0020 | t0002 | g0209 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0356 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02293 | hp1 | a0015 | c0017 | t0003 | g0067 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02300 | hp2 | a0003 | c0003 | t0002 | g0189 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02451 | hp1 | a0008 | c0009 | t0006 | g0012 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02451 | hp2 | a0006 | c0007 | t0001 | g0019 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0032 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02572 | hp1 | a0004 | c0004 | t0001 | g0357 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02572 | hp2 | a0005 | c0005 | t0002 | g0144 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02602 | hp2 | a0002 | c0002 | t0003 | g0085 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02622 | hp1 | a0004 | c0011 | t0001 | g0261 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02622 | hp2 | a0005 | c0005 | t0002 | g0205 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02630 | hp1 | a0004 | c0004 | t0001 | g0242 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02647 | hp2 | a0004 | c0004 | t0001 | g0254 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0148 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02698 | hp2 | a0002 | c0028 | t0003 | g0073 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02717 | hp1 | a0004 | c0011 | t0001 | g0346 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02717 | hp2 | a0005 | c0005 | t0002 | g0143 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02735 | hp1 | a0003 | c0003 | t0002 | g0168 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0034 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02738 | hp1 | a0002 | c0002 | t0003 | g0024 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02738 | hp2 | a0001 | c0001 | t0012 | g0220 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02818 | hp1 | a0004 | c0004 | t0001 | g0245 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02818 | hp2 | a0003 | c0003 | t0002 | g0163 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02886 | hp2 | a0004 | c0004 | t0001 | g0257 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02895 | hp1 | a0005 | c0015 | t0002 | g0176 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02895 | hp2 | a0011 | c0012 | t0001 | g0127 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02896 | hp1 | a0008 | c0009 | t0006 | g0010 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02896 | hp2 | a0005 | c0005 | t0002 | g0161 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02897 | hp1 | a0011 | c0012 | t0001 | g0128 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02897 | hp2 | a0005 | c0005 | t0002 | g0178 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02922 | hp1 | a0006 | c0007 | t0001 | g0030 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02922 | hp2 | a0005 | c0005 | t0002 | g0206 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02965 | hp1 | a0005 | c0005 | t0002 | g0201 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02965 | hp2 | a0005 | c0005 | t0002 | g0208 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02976 | hp1 | a0004 | c0004 | t0001 | g0355 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03017 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03041 | hp1 | a0006 | c0007 | t0001 | g0020 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0248 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03098 | hp2 | a0005 | c0015 | t0002 | g0145 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03130 | hp1 | a0014 | c0018 | t0002 | g0204 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03130 | hp2 | a0004 | c0004 | t0001 | g0250 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03139 | hp1 | a0006 | c0007 | t0001 | g0139 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03139 | hp2 | a0004 | c0004 | t0001 | g0251 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0256 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03225 | hp1 | a0005 | c0005 | t0002 | g0177 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03225 | hp2 | a0011 | c0012 | t0001 | g0031 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0048 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03453 | hp1 | a0024 | c0033 | t0017 | g0146 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0241 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03486 | hp1 | a0004 | c0004 | t0001 | g0259 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03486 | hp2 | a0005 | c0005 | t0002 | g0200 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03490 | hp1 | a0003 | c0003 | t0011 | g0154 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0033 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03491 | hp1 | a0015 | c0017 | t0003 | g0044 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0240 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03516 | hp2 | a0005 | c0005 | t0002 | g0183 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03540 | hp1 | a0004 | c0004 | t0001 | g0246 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03540 | hp2 | a0006 | c0007 | t0001 | g0029 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03654 | hp1 | a0003 | c0003 | t0002 | g0162 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0045 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03710 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03834 | hp1 | a0003 | c0003 | t0002 | g0164 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0096 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0064 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0159 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0082 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0078 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0193 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18522 | hp1 | a0005 | c0005 | t0002 | g0179 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18522 | hp2 | a0025 | c0040 | t0001 | g0211 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18747 | hp1 | a0001 | c0006 | t0001 | g0225 | EAS | CHB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18944 | hp2 | a0026 | c0026 | t0003 | g0004 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18945 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18945 | hp2 | a0027 | c0036 | t0001 | g0292 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18946 | hp2 | a0012 | c0014 | t0001 | g0133 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18950 | hp1 | a0013 | c0016 | t0003 | g0125 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18950 | hp2 | a0009 | c0010 | t0001 | g0213 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18951 | hp1 | a0003 | c0003 | t0002 | g0165 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18957 | hp2 | a0003 | c0003 | t0002 | g0180 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18960 | hp2 | a0002 | c0024 | t0001 | g0100 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18961 | hp2 | a0003 | c0003 | t0002 | g0197 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18962 | hp1 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18964 | hp2 | a0001 | c0006 | t0001 | g0227 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18965 | hp2 | a0002 | c0002 | t0016 | g0091 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18967 | hp1 | a0003 | c0003 | t0002 | g0151 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18967 | hp2 | a0028 | c0032 | t0001 | g0107 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18970 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18972 | hp1 | a0001 | c0038 | t0001 | g0232 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18973 | hp1 | a0001 | c0006 | t0001 | g0358 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18974 | hp1 | a0029 | c0035 | t0001 | g0266 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18978 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18979 | hp1 | a0012 | c0014 | t0001 | g0086 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18979 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18983 | hp1 | a0009 | c0010 | t0001 | g0215 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18983 | hp2 | a0010 | c0013 | t0001 | g0023 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0074 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18989 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18990 | hp1 | a0002 | c0002 | t0008 | g0013 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18991 | hp1 | a0001 | c0006 | t0001 | g0230 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18993 | hp1 | a0001 | c0006 | t0001 | g0237 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18993 | hp2 | a0012 | c0014 | t0001 | g0097 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18994 | hp2 | a0016 | c0019 | t0003 | g0079 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19001 | hp1 | a0003 | c0003 | t0010 | g0150 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19001 | hp2 | a0030 | c0027 | t0001 | g0109 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19002 | hp1 | a0009 | c0010 | t0001 | g0352 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19003 | hp1 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19005 | hp2 | a0002 | c0002 | t0003 | g0043 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19007 | hp1 | a0010 | c0013 | t0001 | g0105 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19009 | hp2 | a0001 | c0006 | t0001 | g0223 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19010 | hp2 | a0001 | c0006 | t0001 | g0233 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19011 | hp1 | a0003 | c0003 | t0002 | g0190 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19011 | hp2 | a0002 | c0002 | t0003 | g0080 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19012 | hp1 | a0016 | c0019 | t0003 | g0063 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19030 | hp1 | a0004 | c0004 | t0001 | g0252 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19043 | hp1 | a0004 | c0004 | t0001 | g0249 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19043 | hp2 | a0005 | c0005 | t0002 | g0171 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19056 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0129 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19060 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19060 | hp2 | a0031 | c0031 | t0002 | g0001 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19070 | hp1 | a0001 | c0006 | t0001 | g0231 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19075 | hp1 | a0002 | c0002 | t0003 | g0132 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19075 | hp2 | a0001 | c0006 | t0001 | g0234 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19085 | hp2 | a0001 | c0006 | t0001 | g0229 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19090 | hp1 | a0009 | c0010 | t0001 | g0214 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19240 | hp1 | a0032 | c0023 | t0006 | g0011 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA19240 | hp2 | a0033 | c0042 | t0001 | g0258 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20129 | hp1 | a0008 | c0009 | t0007 | g0009 | AFR | ASW | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20129 | hp2 | a0002 | c0025 | t0001 | g0136 | AFR | ASW | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20805 | hp1 | a0002 | c0002 | t0003 | g0022 | EUR | TSI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | GIH | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20905 | hp2 | a0003 | c0003 | t0002 | g0167 | SAS | GIH | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01123 | hp1 | a0018 | c0030 | t0002 | g0192 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02109 | hp2 | a0005 | c0005 | t0002 | g0170 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02486 | hp1 | a0002 | c0022 | t0015 | g0008 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0061 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02559 | hp1 | a0006 | c0007 | t0001 | g0021 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG02559 | hp2 | a0004 | c0004 | t0001 | g0243 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03471 | hp1 | a0006 | c0007 | t0001 | g0138 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG03471 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0247 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
HG06807 | hp2 | a0005 | c0015 | t0002 | g0175 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20300 | hp1 | a0005 | c0005 | t0002 | g0160 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0255 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
NA21309 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0098 | REF | REF | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0348 | REF | REF | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40606445 | G | C | 24 | a0002 a0003 a0005 others(21): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
missense_variant | MODERATE | c.128G>C | p.Arg43Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/26 | 289/9266 | 128/6951 | 43/2316 | chr15 | 40606445 | |||
chr15:40610276 | G | A | 1 | a0023 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.229G>A | p.Val77Met | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/26 | 390/9266 | 229/6951 | 77/2316 | chr15 | 40610276 | |||
chr15:40610292 | T | C | 2 | a0006 a0011 |
12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
missense_variant | MODERATE | c.245T>C | p.Met82Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/26 | 406/9266 | 245/6951 | 82/2316 | chr15 | 40610292 | |||
chr15:40611486 | A | G | 26 | a0002 a0003 a0004 others(23): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
missense_variant | MODERATE | c.259A>G | p.Thr87Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/26 | 420/9266 | 259/6951 | 87/2316 | chr15 | 40611486 | |||
chr15:40620715 | A | G | 1 | a0033 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.451A>G | p.Met151Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 612/9266 | 451/6951 | 151/2316 | chr15 | 40620715 | |||
chr15:40620761 | T | C | 1 | a0021 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.497T>C | p.Leu166Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 658/9266 | 497/6951 | 166/2316 | chr15 | 40620761 | |||
chr15:40620835 | G | A | 1 | a0029 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.571G>A | p.Glu191Lys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 732/9266 | 571/6951 | 191/2316 | chr15 | 40620835 | |||
chr15:40620991 | A | G | 1 | a0017 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.727A>G | p.Ile243Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 888/9266 | 727/6951 | 243/2316 | chr15 | 40620991 | |||
chr15:40621033 | A | G | 1 | a0016 | 2 | NA18994.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.769A>G | p.Met257Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 930/9266 | 769/6951 | 257/2316 | chr15 | 40621033 | |||
chr15:40621076 | C | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.812C>G | p.Thr271Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 973/9266 | 812/6951 | 271/2316 | chr15 | 40621076 | |||
chr15:40621258 | G | C | 1 | a0027 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.994G>C | p.Ala332Pro | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1155/9266 | 994/6951 | 332/2316 | chr15 | 40621258 | |||
chr15:40621393 | A | G | 1 | a0014 | 2 | HG02055.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1129A>G | p.Ile377Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1290/9266 | 1129/6951 | 377/2316 | chr15 | 40621393 | |||
chr15:40621642 | G | T | 24 | a0002 a0003 a0005 others(21): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
missense_variant | MODERATE | c.1378G>T | p.Ala460Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1539/9266 | 1378/6951 | 460/2316 | chr15 | 40621642 | |||
chr15:40621742 | C | T | 1 | a0028 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1478C>T | p.Ala493Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1639/9266 | 1478/6951 | 493/2316 | chr15 | 40621742 | |||
chr15:40621757 | T | A | 3 | a0008 a0011 a0032 |
8 | HG01109.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.1493T>A | p.Ile498Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1654/9266 | 1493/6951 | 498/2316 | chr15 | 40621757 | |||
chr15:40621979 | T | C | 14 | a0002 a0006 a0007 others(11): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
missense_variant | MODERATE | c.1715T>C | p.Met572Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1876/9266 | 1715/6951 | 572/2316 | chr15 | 40621979 | |||
chr15:40622018 | A | G | 1 | a0031 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1754A>G | p.Gln585Arg | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1915/9266 | 1754/6951 | 585/2316 | chr15 | 40622018 | |||
chr15:40622278 | A | C | 1 | a0033 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2014A>C | p.Ile672Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2175/9266 | 2014/6951 | 672/2316 | chr15 | 40622278 | |||
chr15:40622633 | C | G | 1 | a0015 | 2 | HG02293.hp1 HG03491.hp1 |
missense_variant | MODERATE | c.2369C>G | p.Thr790Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2530/9266 | 2369/6951 | 790/2316 | chr15 | 40622633 | |||
chr15:40622992 | A | G | 26 | a0002 a0003 a0004 others(23): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
missense_variant | MODERATE | c.2728A>G | p.Arg910Gly | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2889/9266 | 2728/6951 | 910/2316 | chr15 | 40622992 | |||
chr15:40623079 | A | T | 1 | a0018 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.2815A>T | p.Met939Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2976/9266 | 2815/6951 | 939/2316 | chr15 | 40623079 | |||
chr15:40623171 | A | C | 1 | a0012 | 3 | NA18946.hp2 NA18979.hp1 NA18993.hp2 |
missense_variant | MODERATE | c.2907A>C | p.Arg969Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3068/9266 | 2907/6951 | 969/2316 | chr15 | 40623171 | |||
chr15:40623754 | C | G | 2 | a0008 a0032 |
5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.3490C>G | p.Leu1164Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3651/9266 | 3490/6951 | 1164/2316 | chr15 | 40623754 | |||
chr15:40623923 | G | T | 1 | a0020 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.3659G>T | p.Gly1220Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3820/9266 | 3659/6951 | 1220/2316 | chr15 | 40623923 | |||
chr15:40624013 | C | T | 1 | a0025 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3749C>T | p.Ala1250Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3910/9266 | 3749/6951 | 1250/2316 | chr15 | 40624013 | |||
chr15:40624039 | A | G | 3 | a0003 a0018 a0031 |
50 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(47): Show |
missense_variant | MODERATE | c.3775A>G | p.Lys1259Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3936/9266 | 3775/6951 | 1259/2316 | chr15 | 40624039 | |||
chr15:40624264 | C | T | 1 | a0013 | 2 | HG00544.hp2 NA18950.hp1 |
missense_variant | MODERATE | c.4000C>T | p.Pro1334Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4161/9266 | 4000/6951 | 1334/2316 | chr15 | 40624264 | |||
chr15:40624434 | T | A | 3 | a0010 a0012 a0028 |
7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
missense_variant | MODERATE | c.4170T>A | p.Asp1390Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4331/9266 | 4170/6951 | 1390/2316 | chr15 | 40624434 | |||
chr15:40624603 | A | G | 1 | a0007 | 7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
missense_variant | MODERATE | c.4339A>G | p.Thr1447Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4500/9266 | 4339/6951 | 1447/2316 | chr15 | 40624603 | |||
chr15:40624766 | C | T | 1 | a0016 | 2 | NA18994.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.4502C>T | p.Ala1501Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4663/9266 | 4502/6951 | 1501/2316 | chr15 | 40624766 | |||
chr15:40624837 | A | G | 1 | a0030 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.4573A>G | p.Asn1525Asp | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4734/9266 | 4573/6951 | 1525/2316 | chr15 | 40624837 | |||
chr15:40625036 | A | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.4772A>G | p.Asn1591Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4933/9266 | 4772/6951 | 1591/2316 | chr15 | 40625036 | |||
chr15:40625195 | A | G | 1 | a0017 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.4931A>G | p.Lys1644Arg | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5092/9266 | 4931/6951 | 1644/2316 | chr15 | 40625195 | |||
chr15:40645051 | C | A | 1 | a0026 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.5853C>A | p.Asn1951Lys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/26 | 6014/9266 | 5853/6951 | 1951/2316 | chr15 | 40645051 | |||
chr15:40647014 | A | G | 1 | a0022 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.6034A>G | p.Ile2012Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/26 | 6195/9266 | 6034/6951 | 2012/2316 | chr15 | 40647014 | |||
chr15:40647023 | A | C | 1 | a0009 | 4 | NA18950.hp2 NA18983.hp1 NA19002.hp1 others(1): Show |
missense_variant | MODERATE | c.6043A>C | p.Met2015Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/26 | 6204/9266 | 6043/6951 | 2015/2316 | chr15 | 40647023 | |||
chr15:40662172 | G | A | 1 | a0032 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6935G>A | p.Cys2312Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 7096/9266 | 6935/6951 | 2312/2316 | chr15 | 40662172 | |||
chr15:40662174 | C | T | 1 | a0019 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.6937C>T | p.His2313Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 7098/9266 | 6937/6951 | 2313/2316 | chr15 | 40662174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40621563 | T | C | 1 | a0002c0022 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1299T>C | p.Cys433Cys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1460/9266 | 1299/6951 | 433/2316 | chr15 | 40621563 | |||
chr15:40622532 | A | G | 1 | a0002c0028 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2268A>G | p.Ser756Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2429/9266 | 2268/6951 | 756/2316 | chr15 | 40622532 | |||
chr15:40622574 | C | T | 18 | a0002c0002 a0002c0022 a0002c0024 others(15): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
synonymous_variant | LOW | c.2310C>T | p.Val770Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2471/9266 | 2310/6951 | 770/2316 | chr15 | 40622574 | |||
chr15:40622847 | T | G | 18 | a0002c0002 a0002c0022 a0002c0024 others(15): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
synonymous_variant | LOW | c.2583T>G | p.Thr861Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2744/9266 | 2583/6951 | 861/2316 | chr15 | 40622847 | |||
chr15:40623429 | T | C | 1 | a0002c0024 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.3165T>C | p.Asn1055Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3326/9266 | 3165/6951 | 1055/2316 | chr15 | 40623429 | |||
chr15:40623669 | C | T | 3 | a0010c0013 a0012c0014 a0028c0032 |
7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
synonymous_variant | LOW | c.3405C>T | p.Ala1135Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3566/9266 | 3405/6951 | 1135/2316 | chr15 | 40623669 | |||
chr15:40623696 | T | C | 18 | a0002c0002 a0002c0022 a0002c0024 others(15): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
synonymous_variant | LOW | c.3432T>C | p.Asn1144Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3593/9266 | 3432/6951 | 1144/2316 | chr15 | 40623696 | |||
chr15:40624026 | A | G | 1 | a0001c0039 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.3762A>G | p.Glu1254Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3923/9266 | 3762/6951 | 1254/2316 | chr15 | 40624026 | |||
chr15:40624074 | G | A | 1 | a0005c0015 | 3 | HG02895.hp1 HG03098.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3810G>A | p.Ala1270Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3971/9266 | 3810/6951 | 1270/2316 | chr15 | 40624074 | |||
chr15:40624482 | T | C | 1 | a0002c0025 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.4218T>C | p.Tyr1406Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4379/9266 | 4218/6951 | 1406/2316 | chr15 | 40624482 | |||
chr15:40625415 | T | C | 3 | a0001c0006 a0009c0010 a0020c0041 |
20 | HG00558.hp2 HG00673.hp2 HG01928.hp2 others(17): Show |
synonymous_variant | LOW | c.5151T>C | p.Pro1717Pro | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5312/9266 | 5151/6951 | 1717/2316 | chr15 | 40625415 | |||
chr15:40625535 | C | T | 1 | a0004c0011 | 4 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.5271C>T | p.Cys1757Cys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5432/9266 | 5271/6951 | 1757/2316 | chr15 | 40625535 | |||
chr15:40628126 | A | T | 1 | a0001c0038 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.5433A>T | p.Ile1811Ile | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 11/26 | 5594/9266 | 5433/6951 | 1811/2316 | chr15 | 40628126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40594279 | G | A | 1 | a0002c0002t0008 | 1 | NA18990.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8653 | chr15 | 40594279 | ||||||
chr15:40594355 | G | A | 1 | a0007c0008t0005 | 7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8577 | chr15 | 40594355 | ||||||
chr15:40594381 | T | G | 1 | a0008c0009t0007 | 2 | HG01109.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8551 | chr15 | 40594381 | ||||||
chr15:40662216 | A | G | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 28 | chr15 | 40662216 | ||||||
chr15:40662324 | TATGTTTT others(53): Show |
T | 1 | a0002c0002t0016 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137_*196delATGTTT others(54): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 137 | chr15 | 40662324 | ||||||
chr15:40662393 | A | G | 4 | a0002c0022t0015 a0008c0009t0006 a0008c0009t0007 others(1): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 205 | chr15 | 40662393 | ||||||
chr15:40662538 | A | G | 4 | a0002c0022t0015 a0008c0009t0006 a0008c0009t0007 others(1): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*350A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 350 | chr15 | 40662538 | ||||||
chr15:40662597 | A | G | 1 | a0003c0003t0014 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 409 | chr15 | 40662597 | ||||||
chr15:40662638 | C | T | 1 | a0017c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 450 | chr15 | 40662638 | ||||||
chr15:40662863 | G | C | 1 | a0017c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 675 | chr15 | 40662863 | ||||||
chr15:40662871 | G | A | 12 | a0003c0003t0002 a0003c0003t0010 a0003c0003t0011 others(9): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 683 | chr15 | 40662871 | ||||||
chr15:40662966 | A | G | 1 | a0017c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 778 | chr15 | 40662966 | ||||||
chr15:40663105 | G | GCTGGAGT others(38): Show |
1 | a0002c0022t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922_*966dupAGTGCA others(39): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 967 | INFO_REALIGN_3_PRIME | chr15 | 40663105 | |||||
chr15:40663282 | A | G | 1 | a0003c0003t0011 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1094A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1094 | chr15 | 40663282 | ||||||
chr15:40663441 | T | A | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1253T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1253 | chr15 | 40663441 | ||||||
chr15:40663795 | C | T | 1 | a0003c0003t0010 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1607C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1607 | chr15 | 40663795 | ||||||
chr15:40663862 | G | A | 1 | a0001c0001t0004 | 13 | HG01109.hp1 HG01123.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1674G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1674 | chr15 | 40663862 | ||||||
chr15:40663909 | G | GGTATGTT others(47): Show |
1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721_*1722insGTAT others(50): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1722 | chr15 | 40663909 | ||||||
chr15:40663910 | A | T | 1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1722A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1722 | chr15 | 40663910 | ||||||
chr15:40663911 | G | T | 1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1723G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1723 | chr15 | 40663911 | ||||||
chr15:40664053 | A | C | 1 | a0022c0029t0009 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1865 | chr15 | 40664053 | ||||||
chr15:40664118 | G | A | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1930G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1930 | chr15 | 40664118 | ||||||
chr15:40664154 | G | A | 1 | a0017c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1966G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1966 | chr15 | 40664154 | ||||||
chr15:40664273 | A | C | 7 | a0002c0002t0003 a0002c0028t0003 a0007c0008t0005 others(4): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2085A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 2085 | chr15 | 40664273 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40594423 | T | C | 136 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(133): Show |
138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18+31T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594423 | |||||||
chr15:40594469 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | NA18957.hp1 NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-18+77G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594469 | |||||||
chr15:40594613 | T | C | 1 | a0005c0005t0002g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+221T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594613 | |||||||
chr15:40594625 | C | T | 2 | a0006c0007t0001g0138 a0006c0007t0001g0139 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+233C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594625 | |||||||
chr15:40594643 | C | T | 5 | a0003c0003t0002g0359 a0003c0003t0002g0360 a0003c0003t0002g0361 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+251C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594643 | |||||||
chr15:40594677 | C | A | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+285C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594677 | |||||||
chr15:40594694 | C | G | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+302C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594694 | |||||||
chr15:40594790 | T | C | 1 | a0005c0005t0002g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-18+398T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594790 | |||||||
chr15:40594791 | T | A | 1 | a0002c0002t0008g0013 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18+399T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594791 | |||||||
chr15:40594900 | T | C | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+508T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594900 | |||||||
chr15:40594958 | T | C | 1 | a0002c0002t0003g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18+566T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594958 | |||||||
chr15:40595456 | T | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+1064T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595456 | |||||||
chr15:40595565 | G | T | 1 | a0001c0006t0001g0358 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-18+1173G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595565 | |||||||
chr15:40595603 | T | G | 1 | a0002c0002t0003g0016 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-18+1211T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595603 | |||||||
chr15:40595787 | C | A | 207 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-18+1395C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595787 | |||||||
chr15:40595805 | T | C | 5 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+1413T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595805 | |||||||
chr15:40595813 | A | G | 7 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(4): Show |
7 | HG00741.hp1 HG01109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1421A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595813 | |||||||
chr15:40595836 | G | A | 2 | a0001c0001t0001g0210 a0025c0040t0001g0211 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+1444G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595836 | |||||||
chr15:40596029 | TA | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1644delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40596029 | ||||||
chr15:40596046 | C | T | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+1654C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596046 | |||||||
chr15:40596124 | G | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1732G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596124 | |||||||
chr15:40596401 | G | A | 1 | a0002c0002t0003g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18+2009G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596401 | |||||||
chr15:40596555 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-18+2163T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596555 | |||||||
chr15:40596577 | A | G | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2185A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596577 | |||||||
chr15:40596601 | C | G | 1 | a0003c0003t0002g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-18+2209C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596601 | |||||||
chr15:40596686 | C | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2294C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596686 | |||||||
chr15:40596838 | T | C | 1 | a0010c0013t0001g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18+2446T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596838 | |||||||
chr15:40596993 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18+2601T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596993 | |||||||
chr15:40597000 | CA | C | 86 | a0001c0001t0001g0353 a0001c0001t0001g0354 a0002c0002t0001g0025 others(83): Show |
87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-18+2629delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | ||||||
chr15:40597000 | CAA | C | 116 | a0002c0002t0001g0087 a0002c0002t0001g0088 a0002c0002t0001g0089 others(113): Show |
118 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-18+2628_-18+2629d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | ||||||
chr15:40597000 | CAAA | C | 8 | a0002c0002t0001g0134 a0002c0002t0003g0129 a0002c0002t0003g0130 others(5): Show |
8 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+2627_-18+2629d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | ||||||
chr15:40597021 | A | G | 1 | a0003c0003t0002g0147 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-18+2629A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597021 | |||||||
chr15:40597054 | A | G | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2662A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597054 | |||||||
chr15:40597215 | G | C | 28 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(25): Show |
28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+2823G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597215 | |||||||
chr15:40597240 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+2848C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597240 | |||||||
chr15:40597372 | A | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-18+2980A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597372 | |||||||
chr15:40597411 | T | C | 5 | a0008c0009t0006g0010 a0008c0009t0006g0012 a0008c0009t0007g0007 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+3019T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597411 | |||||||
chr15:40597564 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-18+3172C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597564 | |||||||
chr15:40597626 | T | C | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-18+3234T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597626 | |||||||
chr15:40597632 | A | T | 1 | a0013c0016t0003g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3240A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597632 | |||||||
chr15:40597633 | T | A | 1 | a0013c0016t0003g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3241T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597633 | |||||||
chr15:40597634 | A | T | 1 | a0013c0016t0003g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3242A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597634 | |||||||
chr15:40597796 | T | G | 4 | a0006c0007t0001g0029 a0006c0007t0001g0030 a0006c0007t0001g0138 others(1): Show |
4 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3404T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597796 | |||||||
chr15:40597929 | T | C | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+3537T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597929 | |||||||
chr15:40598078 | G | A | 1 | a0003c0003t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+3686G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598078 | |||||||
chr15:40598099 | A | G | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-18+3707A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598099 | |||||||
chr15:40598143 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-18+3751T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598143 | |||||||
chr15:40598210 | A | G | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+3818A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598210 | |||||||
chr15:40598212 | T | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+3820T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598212 | |||||||
chr15:40598297 | C | T | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-18+3905C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598297 | |||||||
chr15:40598312 | G | T | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-18+3920G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598312 | |||||||
chr15:40598352 | T | G | 1 | a0004c0011t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3960T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598352 | |||||||
chr15:40598439 | G | A | 2 | a0002c0002t0001g0135 a0002c0025t0001g0136 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-18+4047G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598439 | |||||||
chr15:40598589 | A | C | 1 | a0002c0002t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+4197A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598589 | |||||||
chr15:40598599 | A | G | 2 | a0002c0002t0003g0121 a0002c0002t0003g0122 |
2 | NA18969.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-18+4207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598599 | |||||||
chr15:40598609 | T | G | 3 | a0006c0007t0001g0029 a0006c0007t0001g0138 a0006c0007t0001g0139 |
3 | HG03139.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+4217T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598609 | |||||||
chr15:40598629 | T | G | 1 | a0013c0016t0003g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+4237T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598629 | |||||||
chr15:40598632 | A | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18+4240A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598632 | |||||||
chr15:40598809 | T | A | 3 | a0009c0010t0001g0213 a0009c0010t0001g0214 a0009c0010t0001g0215 |
3 | NA18950.hp2 NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-17-4106T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598809 | |||||||
chr15:40598873 | G | A | 73 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(70): Show |
75 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-4042G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598873 | |||||||
chr15:40599120 | A | T | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-17-3795A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599120 | |||||||
chr15:40599121 | T | A | 227 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.-17-3794T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599121 | |||||||
chr15:40599122 | T | A | 4 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-3793T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599122 | |||||||
chr15:40599260 | C | T | 1 | a0002c0002t0003g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-3655C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599260 | |||||||
chr15:40599312 | C | CA | 18 | a0001c0001t0001g0216 a0001c0001t0001g0262 a0001c0001t0001g0263 others(15): Show |
18 | HG01070.hp2 HG02135.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-3585dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599312 | ||||||
chr15:40599404 | G | A | 1 | a0002c0002t0008g0013 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-17-3511G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599404 | |||||||
chr15:40599419 | T | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3496T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599419 | |||||||
chr15:40599426 | C | T | 3 | a0003c0003t0002g0361 a0003c0003t0002g0362 a0003c0003t0002g0363 |
3 | HG00738.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-17-3489C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599426 | |||||||
chr15:40599454 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-17-3461G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599454 | |||||||
chr15:40599487 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3428G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599487 | |||||||
chr15:40599515 | C | T | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-17-3400C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599515 | |||||||
chr15:40599516 | T | C | 1 | a0003c0003t0002g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-17-3399T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599516 | |||||||
chr15:40599571 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3344G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599571 | |||||||
chr15:40599584 | G | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3331G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599584 | |||||||
chr15:40599619 | G | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3296G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599619 | |||||||
chr15:40599661 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-3254G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599661 | |||||||
chr15:40599793 | CT | C | 148 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0210 others(145): Show |
150 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-17-3101delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | ||||||
chr15:40599793 | CTT | C | 203 | a0001c0001t0001g0140 a0001c0001t0001g0217 a0001c0001t0001g0267 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-17-3102_-17-3101d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | ||||||
chr15:40599793 | CTTT | C | 8 | a0002c0002t0001g0087 a0002c0002t0003g0032 a0002c0002t0003g0033 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-3103_-17-3101d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | ||||||
chr15:40600003 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2912C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600003 | |||||||
chr15:40600005 | A | C | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2910A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600005 | |||||||
chr15:40600075 | C | CT | 7 | a0001c0001t0001g0345 a0001c0001t0001g0351 a0001c0039t0001g0347 others(4): Show |
7 | HG00544.hp1 HG00642.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-2822dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40600075 | ||||||
chr15:40600075 | CT | C | 202 | a0001c0001t0001g0272 a0002c0002t0001g0025 a0002c0002t0001g0026 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-17-2822delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40600075 | ||||||
chr15:40600207 | C | G | 1 | a0006c0007t0001g0030 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-2708C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600207 | |||||||
chr15:40600236 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-2679G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600236 | |||||||
chr15:40600364 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2551C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600364 | |||||||
chr15:40600366 | C | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2549C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600366 | |||||||
chr15:40600403 | G | A | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.-17-2512G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600403 | |||||||
chr15:40600478 | T | C | 1 | a0011c0012t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-2437T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600478 | |||||||
chr15:40600499 | A | T | 1 | a0002c0002t0003g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-2416A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600499 | |||||||
chr15:40600523 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-2392A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600523 | |||||||
chr15:40600841 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2074C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600841 | |||||||
chr15:40601023 | C | G | 8 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-1892C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601023 | |||||||
chr15:40601024 | T | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1891T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601024 | |||||||
chr15:40601043 | C | T | 1 | a0007c0008t0005g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-17-1872C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601043 | |||||||
chr15:40601268 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1647C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601268 | |||||||
chr15:40601301 | T | A | 1 | a0002c0002t0001g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1614T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601301 | |||||||
chr15:40601320 | C | A | 209 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-17-1595C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601320 | |||||||
chr15:40601375 | C | A | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.-17-1540C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601375 | |||||||
chr15:40601611 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-1304C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601611 | |||||||
chr15:40601688 | G | T | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-1227G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601688 | |||||||
chr15:40601741 | T | G | 1 | a0013c0016t0003g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-17-1174T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601741 | |||||||
chr15:40601778 | A | C | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-1137A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601778 | |||||||
chr15:40601827 | C | CA | 74 | a0001c0001t0001g0273 a0001c0001t0012g0220 a0002c0002t0001g0088 others(71): Show |
76 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-17-1073dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601827 | ||||||
chr15:40601827 | C | CAA | 8 | a0002c0002t0003g0024 a0002c0002t0003g0037 a0002c0002t0003g0039 others(5): Show |
8 | HG00544.hp2 HG00642.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-1074_-17-1073d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601827 | ||||||
chr15:40601859 | C | CT | 152 | a0001c0001t0001g0140 a0001c0001t0001g0210 a0001c0001t0001g0216 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-17-1030dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | ||||||
chr15:40601859 | C | CTT | 84 | a0001c0001t0001g0342 a0002c0002t0001g0025 a0002c0002t0001g0026 others(81): Show |
85 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-17-1031_-17-1030d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | ||||||
chr15:40601859 | C | CTTT | 24 | a0002c0002t0001g0028 a0002c0002t0001g0087 a0002c0002t0001g0110 others(21): Show |
24 | HG00423.hp1 HG01071.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17-1032_-17-1030d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | ||||||
chr15:40601859 | CTTTTTTT others(4): Show |
C | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-1040_-17-1030d others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | ||||||
chr15:40601955 | C | T | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-960C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601955 | |||||||
chr15:40602053 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-862G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602053 | |||||||
chr15:40602175 | C | T | 1 | a0002c0002t0003g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-17-740C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602175 | |||||||
chr15:40602215 | A | G | 1 | a0006c0007t0001g0139 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-700A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602215 | |||||||
chr15:40602279 | C | T | 1 | a0022c0029t0009g0191 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-636C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602279 | |||||||
chr15:40602303 | A | AT | 63 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(60): Show |
63 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-17-599dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | ||||||
chr15:40602303 | A | ATT | 108 | a0001c0001t0012g0220 a0002c0002t0001g0025 a0002c0002t0001g0026 others(105): Show |
110 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-17-600_-17-599dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | ||||||
chr15:40602303 | A | ATTT | 8 | a0002c0002t0001g0028 a0002c0002t0001g0108 a0002c0002t0001g0115 others(5): Show |
8 | HG00673.hp1 HG02647.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-601_-17-599dup others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | ||||||
chr15:40602338 | G | C | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-577G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602338 | |||||||
chr15:40602363 | C | T | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-17-552C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602363 | |||||||
chr15:40602387 | C | T | 1 | a0002c0002t0003g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-17-528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602387 | |||||||
chr15:40602388 | G | A | 7 | a0001c0001t0001g0262 a0001c0001t0001g0273 a0001c0001t0001g0274 others(4): Show |
7 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-527G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602388 | |||||||
chr15:40602423 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-492A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602423 | |||||||
chr15:40602479 | C | CGTT | 3 | a0002c0022t0015g0008 a0008c0009t0007g0007 a0008c0009t0007g0009 |
3 | HG01109.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17-436_-17-435ins others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602479 | |||||||
chr15:40602479 | C | CGTTT | 3 | a0008c0009t0006g0010 a0008c0009t0006g0012 a0032c0023t0006g0011 |
3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17-436_-17-435ins others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602479 | |||||||
chr15:40602480 | C | CT | 132 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(129): Show |
134 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.-17-413dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | ||||||
chr15:40602480 | C | CTT | 21 | a0001c0006t0001g0231 a0001c0006t0001g0237 a0002c0002t0001g0090 others(18): Show |
21 | HG00741.hp1 HG02602.hp2 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-414_-17-413dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | ||||||
chr15:40602480 | C | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-435C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602480 | |||||||
chr15:40602480 | CT | C | 65 | a0001c0001t0001g0309 a0003c0003t0002g0001 a0003c0003t0002g0147 others(62): Show |
66 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-17-413delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | ||||||
chr15:40602517 | G | A | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-17-398G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602517 | |||||||
chr15:40602559 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-356T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602559 | |||||||
chr15:40602637 | C | A | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-278C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602637 | |||||||
chr15:40602862 | G | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-53G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602862 | |||||||
chr15:40603100 | T | A | 2 | a0003c0003t0002g0184 a0003c0003t0002g0189 |
2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.35+134T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603100 | |||||||
chr15:40603101 | A | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35+135A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603101 | |||||||
chr15:40603242 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.35+276T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603242 | |||||||
chr15:40603402 | A | G | 290 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.35+436A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603402 | |||||||
chr15:40603417 | T | A | 1 | a0002c0002t0003g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.35+451T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603417 | |||||||
chr15:40603432 | T | G | 3 | a0002c0002t0003g0040 a0002c0002t0003g0041 a0002c0002t0003g0066 |
3 | NA18960.hp1 NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.35+466T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603432 | |||||||
chr15:40603573 | A | G | 5 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+607A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603573 | |||||||
chr15:40603610 | A | C | 1 | a0002c0002t0003g0137 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.35+644A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603610 | |||||||
chr15:40603866 | T | C | 12 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(9): Show |
12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.35+900T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603866 | |||||||
chr15:40604090 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.36-1020C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604090 | |||||||
chr15:40604098 | T | C | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.36-1012T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604098 | |||||||
chr15:40604116 | T | TATC | 89 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0310 others(86): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.36-960_36-958dupAT others(1): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604116 | ||||||
chr15:40604116 | TATC | T | 16 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 others(13): Show |
16 | HG00741.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-960_36-958delAT others(1): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604116 | ||||||
chr15:40604193 | TCCTATCT others(45): Show |
T | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.36-873_36-822delAA others(50): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604193 | ||||||
chr15:40604303 | C | T | 1 | a0005c0005t0002g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.36-807C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604303 | |||||||
chr15:40604328 | G | A | 1 | a0002c0002t0003g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.36-782G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604328 | |||||||
chr15:40604590 | C | T | 1 | a0003c0003t0002g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.36-520C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604590 | |||||||
chr15:40604613 | G | A | 10 | a0001c0006t0001g0223 a0001c0006t0001g0224 a0001c0006t0001g0225 others(7): Show |
10 | HG00558.hp2 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.36-497G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604613 | |||||||
chr15:40604907 | A | G | 1 | a0002c0002t0003g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.36-203A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604907 | |||||||
chr15:40604974 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.36-136A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604974 | |||||||
chr15:40605169 | A | G | 1 | a0002c0002t0003g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.75+20A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605169 | |||||||
chr15:40605207 | A | G | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.75+58A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605207 | |||||||
chr15:40605388 | G | A | 71 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(68): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.75+239G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605388 | |||||||
chr15:40605490 | C | T | 9 | a0002c0002t0003g0060 a0002c0002t0003g0062 a0005c0005t0002g0205 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+341C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605490 | |||||||
chr15:40605690 | T | C | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.75+541T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605690 | |||||||
chr15:40605737 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+588A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605737 | |||||||
chr15:40605819 | C | T | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.76-574C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605819 | |||||||
chr15:40605938 | C | G | 1 | a0001c0001t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.76-455C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605938 | |||||||
chr15:40605943 | A | G | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.76-450A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605943 | |||||||
chr15:40605990 | A | T | 1 | a0003c0003t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.76-403A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605990 | |||||||
chr15:40606225 | T | C | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.76-168T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40606225 | |||||||
chr15:40606590 | G | A | 36 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(33): Show |
36 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.135+138G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606590 | |||||||
chr15:40606823 | G | A | 5 | a0005c0005t0002g0206 a0005c0005t0002g0208 a0014c0018t0002g0203 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+371G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606823 | |||||||
chr15:40606850 | C | G | 1 | a0002c0002t0003g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.135+398C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606850 | |||||||
chr15:40606863 | G | A | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.135+411G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606863 | |||||||
chr15:40607055 | C | G | 11 | a0002c0002t0003g0004 a0002c0002t0003g0039 a0002c0002t0003g0055 others(8): Show |
11 | HG01192.hp2 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+603C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607055 | |||||||
chr15:40607246 | G | A | 4 | a0006c0007t0001g0029 a0006c0007t0001g0030 a0006c0007t0001g0138 others(1): Show |
4 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+794G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607246 | |||||||
chr15:40607293 | C | T | 6 | a0007c0008t0005g0002 a0007c0008t0005g0038 a0007c0008t0005g0053 others(3): Show |
7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+841C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607293 | |||||||
chr15:40607297 | T | C | 24 | a0004c0004t0001g0240 a0004c0004t0001g0241 a0004c0004t0001g0242 others(21): Show |
24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.135+845T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607297 | |||||||
chr15:40607361 | A | T | 5 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+909A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607361 | |||||||
chr15:40607495 | A | G | 12 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(9): Show |
12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+1043A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607495 | |||||||
chr15:40607665 | G | T | 1 | a0004c0004t0001g0355 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136-1182G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607665 | |||||||
chr15:40607793 | A | G | 1 | a0001c0038t0001g0232 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.136-1054A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607793 | |||||||
chr15:40607801 | T | A | 1 | a0002c0002t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.136-1046T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607801 | |||||||
chr15:40607894 | C | G | 1 | a0003c0003t0002g0180 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.136-953C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607894 | |||||||
chr15:40608036 | G | A | 1 | a0002c0002t0003g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136-811G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608036 | |||||||
chr15:40608081 | TGTG | T | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.136-763_136-761del others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608081 | ||||||
chr15:40608139 | C | G | 9 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-708C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608139 | |||||||
chr15:40608426 | C | T | 1 | a0002c0002t0003g0052 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.136-421C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608426 | |||||||
chr15:40608433 | G | GA | 10 | a0001c0006t0001g0223 a0001c0038t0001g0232 a0002c0002t0001g0115 others(7): Show |
10 | HG00597.hp2 HG02027.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-392dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608433 | ||||||
chr15:40608433 | GA | G | 24 | a0001c0001t0001g0142 a0002c0002t0001g0126 a0004c0004t0001g0240 others(21): Show |
24 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-392delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608433 | ||||||
chr15:40608511 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.136-336C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608511 | |||||||
chr15:40608521 | C | G | 290 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.136-326C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608521 | |||||||
chr15:40608544 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-303G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608544 | |||||||
chr15:40608606 | G | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-241G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608606 | |||||||
chr15:40608675 | G | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-172G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608675 | |||||||
chr15:40608704 | C | T | 7 | a0001c0006t0001g0223 a0001c0006t0001g0226 a0001c0006t0001g0227 others(4): Show |
7 | HG00558.hp2 HG00673.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-143C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608704 | |||||||
chr15:40608745 | CA | C | 130 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(127): Show |
132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.136-86delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608745 | ||||||
chr15:40609002 | T | C | 1 | a0002c0002t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.197+94T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609002 | |||||||
chr15:40609127 | G | T | 4 | a0002c0002t0003g0039 a0002c0002t0003g0058 a0002c0002t0003g0060 others(1): Show |
4 | NA18970.hp2 NA18999.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+219G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609127 | |||||||
chr15:40609202 | G | A | 1 | a0008c0009t0007g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.197+294G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609202 | |||||||
chr15:40609210 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197+302C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609210 | |||||||
chr15:40609244 | C | CA | 36 | a0001c0001t0001g0212 a0001c0001t0001g0271 a0001c0001t0001g0277 others(33): Show |
36 | HG00408.hp1 HG00621.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.197+357dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr15 | 40609244 | ||||||
chr15:40609244 | CA | C | 13 | a0002c0002t0001g0099 a0002c0002t0001g0108 a0002c0002t0001g0110 others(10): Show |
13 | HG01167.hp2 HG02897.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.197+357delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr15 | 40609244 | ||||||
chr15:40609805 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198-440A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609805 | |||||||
chr15:40609934 | G | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198-311G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609934 | |||||||
chr15:40610438 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.250+141C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40610438 | |||||||
chr15:40610853 | G | A | 8 | a0003c0003t0002g0181 a0005c0005t0002g0205 a0005c0005t0002g0206 others(5): Show |
8 | HG00280.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+556G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40610853 | |||||||
chr15:40611108 | AT | A | 235 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.251-356delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr15 | 40611108 | ||||||
chr15:40611240 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.251-238C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611240 | |||||||
chr15:40611258 | G | A | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251-220G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611258 | |||||||
chr15:40611308 | C | T | 2 | a0011c0012t0001g0127 a0011c0012t0001g0128 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.251-170C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611308 | |||||||
chr15:40611328 | C | T | 1 | a0003c0003t0014g0188 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.251-150C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611328 | |||||||
chr15:40611329 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.251-149G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611329 | |||||||
chr15:40611358 | C | T | 1 | a0002c0002t0003g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.251-120C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611358 | |||||||
chr15:40611392 | C | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0351 |
2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.251-86C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611392 | |||||||
chr15:40611419 | T | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.251-59T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611419 | |||||||
chr15:40611544 | A | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+33A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611544 | |||||||
chr15:40611554 | A | G | 1 | a0003c0003t0002g0180 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.284+43A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611554 | |||||||
chr15:40611616 | C | A | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.284+105C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611616 | |||||||
chr15:40611684 | A | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.284+173A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611684 | |||||||
chr15:40611873 | G | A | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.284+362G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611873 | |||||||
chr15:40611946 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.284+435G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611946 | |||||||
chr15:40611977 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.284+466C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611977 | |||||||
chr15:40611996 | A | G | 9 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+485A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611996 | |||||||
chr15:40612024 | A | G | 1 | a0002c0002t0003g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+513A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612024 | |||||||
chr15:40612039 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.284+528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612039 | |||||||
chr15:40612048 | T | G | 1 | a0001c0006t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.284+537T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612048 | |||||||
chr15:40612323 | C | CA | 7 | a0001c0001t0001g0278 a0001c0001t0001g0311 a0001c0001t0004g0279 others(4): Show |
7 | HG00597.hp2 HG01123.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+820dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40612323 | ||||||
chr15:40612331 | A | C | 68 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(65): Show |
70 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.284+820A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612331 | |||||||
chr15:40612332 | C | A | 42 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0087 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.284+821C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612332 | |||||||
chr15:40612345 | G | A | 6 | a0001c0001t0001g0271 a0001c0001t0001g0305 a0001c0001t0001g0327 others(3): Show |
6 | NA18951.hp2 NA18962.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+834G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612345 | |||||||
chr15:40612407 | G | T | 1 | a0001c0001t0001g0308 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.284+896G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612407 | |||||||
chr15:40612610 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284+1099G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612610 | |||||||
chr15:40612804 | A | C | 1 | a0001c0001t0012g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284+1293A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612804 | |||||||
chr15:40612903 | A | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+1392A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612903 | |||||||
chr15:40612984 | C | T | 1 | a0008c0009t0006g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.284+1473C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612984 | |||||||
chr15:40613104 | A | G | 1 | a0001c0006t0001g0230 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.284+1593A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613104 | |||||||
chr15:40613155 | G | A | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.284+1644G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613155 | |||||||
chr15:40613250 | A | AGT | 5 | a0002c0002t0003g0057 a0008c0009t0006g0010 a0008c0009t0007g0007 others(2): Show |
5 | HG01109.hp2 HG02273.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+1740_284+1741i others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40613250 | ||||||
chr15:40613252 | C | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.284+1741C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613252 | |||||||
chr15:40613359 | T | C | 7 | a0001c0001t0001g0262 a0001c0001t0001g0273 a0001c0001t0001g0274 others(4): Show |
7 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+1848T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613359 | |||||||
chr15:40613442 | A | G | 42 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.285-1899A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613442 | |||||||
chr15:40613461 | TGAAAC | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-1876_285-1872d others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40613461 | ||||||
chr15:40613828 | C | T | 1 | a0002c0002t0003g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.285-1513C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613828 | |||||||
chr15:40613883 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-1458C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613883 | |||||||
chr15:40613943 | G | A | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.285-1398G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613943 | |||||||
chr15:40613999 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.285-1342T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613999 | |||||||
chr15:40614089 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.285-1252C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614089 | |||||||
chr15:40614101 | C | CT | 117 | a0001c0001t0001g0335 a0002c0002t0001g0025 a0002c0002t0001g0026 others(114): Show |
119 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.285-1226dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40614101 | ||||||
chr15:40614101 | C | CTT | 15 | a0001c0001t0001g0219 a0002c0002t0003g0024 a0002c0002t0003g0055 others(12): Show |
15 | HG01975.hp2 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.285-1227_285-1226d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40614101 | ||||||
chr15:40614240 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.285-1101G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614240 | |||||||
chr15:40614295 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285-1046A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614295 | |||||||
chr15:40614435 | G | T | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285-906G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614435 | |||||||
chr15:40614541 | C | G | 1 | a0022c0029t0009g0191 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-800C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614541 | |||||||
chr15:40614895 | A | G | 1 | a0029c0035t0001g0266 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285-446A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614895 | |||||||
chr15:40614932 | C | G | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285-409C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614932 | |||||||
chr15:40615469 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+91C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615469 | |||||||
chr15:40615493 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322+115G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615493 | |||||||
chr15:40615608 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+230A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615608 | |||||||
chr15:40615637 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.322+259C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615637 | |||||||
chr15:40615697 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+319G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615697 | |||||||
chr15:40615721 | C | T | 2 | a0001c0001t0001g0325 a0033c0042t0001g0258 |
2 | HG02056.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.322+343C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615721 | |||||||
chr15:40615762 | C | CT | 7 | a0001c0001t0012g0220 a0001c0006t0001g0231 a0002c0002t0003g0024 others(4): Show |
7 | HG02738.hp1 HG02738.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+399dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40615762 | ||||||
chr15:40615779 | T | G | 28 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(25): Show |
28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.322+401T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615779 | |||||||
chr15:40615853 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0012g0220 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.322+475C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615853 | |||||||
chr15:40616009 | A | C | 290 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.322+631A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616009 | |||||||
chr15:40616057 | G | A | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.322+679G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616057 | |||||||
chr15:40616102 | A | G | 7 | a0001c0001t0001g0269 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG01081.hp1 HG01106.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+724A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616102 | |||||||
chr15:40616125 | C | CT | 72 | a0001c0001t0001g0328 a0003c0003t0002g0001 a0003c0003t0002g0147 others(69): Show |
73 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.322+762dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40616125 | ||||||
chr15:40616498 | C | T | 293 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0216 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.322+1120C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616498 | |||||||
chr15:40616563 | G | A | 1 | a0002c0025t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322+1185G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616563 | |||||||
chr15:40616601 | C | T | 1 | a0002c0002t0003g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322+1223C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616601 | |||||||
chr15:40616706 | A | G | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.322+1328A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616706 | |||||||
chr15:40616794 | A | G | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.322+1416A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616794 | |||||||
chr15:40616920 | T | C | 3 | a0003c0003t0002g0361 a0003c0003t0002g0362 a0003c0003t0002g0363 |
3 | HG00738.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.322+1542T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616920 | |||||||
chr15:40617012 | G | T | 37 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(34): Show |
37 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.322+1634G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617012 | |||||||
chr15:40617073 | C | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.322+1695C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617073 | |||||||
chr15:40617255 | C | T | 1 | a0002c0002t0001g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323-1704C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617255 | |||||||
chr15:40617269 | A | G | 70 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(67): Show |
72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.323-1690A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617269 | |||||||
chr15:40617358 | CAA | C | 9 | a0006c0007t0001g0017 a0006c0007t0001g0018 a0006c0007t0001g0019 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.323-1599_323-1598d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617358 | ||||||
chr15:40617419 | A | G | 2 | a0005c0005t0002g0177 a0005c0005t0002g0183 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.323-1540A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617419 | |||||||
chr15:40617498 | T | C | 71 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(68): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.323-1461T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617498 | |||||||
chr15:40617522 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.323-1437G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617522 | |||||||
chr15:40617750 | C | T | 2 | a0003c0003t0002g0149 a0003c0003t0002g0187 |
2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.323-1209C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617750 | |||||||
chr15:40617808 | A | G | 2 | a0016c0019t0003g0063 a0016c0019t0003g0079 |
2 | NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.323-1151A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617808 | |||||||
chr15:40617918 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.323-1041G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617918 | |||||||
chr15:40617939 | A | G | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.323-1020A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617939 | |||||||
chr15:40617975 | T | TA | 14 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0221 others(11): Show |
14 | HG00597.hp1 HG00673.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.323-945dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | T | TAAAA | 7 | a0001c0001t0001g0262 a0001c0001t0001g0273 a0001c0001t0001g0274 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-948_323-945dup others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TA | T | 55 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0212 others(52): Show |
56 | HG00408.hp1 HG00741.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.323-945delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAA | T | 15 | a0001c0001t0001g0222 a0001c0001t0001g0300 a0001c0001t0001g0336 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.323-946_323-945del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAA | T | 9 | a0003c0003t0002g0156 a0003c0003t0002g0157 a0003c0003t0002g0158 others(6): Show |
9 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.323-947_323-945del others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAA | T | 13 | a0003c0003t0002g0147 a0003c0003t0002g0148 a0003c0003t0002g0151 others(10): Show |
13 | HG00639.hp2 HG00738.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.323-948_323-945del others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAA | T | 27 | a0003c0003t0002g0001 a0003c0003t0002g0149 a0003c0003t0002g0152 others(24): Show |
28 | HG00099.hp1 HG00280.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.323-949_323-945del others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAA | T | 10 | a0003c0003t0002g0172 a0003c0003t0002g0173 a0003c0003t0002g0174 others(7): Show |
10 | HG00558.hp1 HG01516.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-950_323-945del others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(1): Show |
T | 17 | a0002c0002t0001g0089 a0002c0002t0001g0108 a0002c0002t0001g0113 others(14): Show |
17 | HG00597.hp2 HG02135.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.323-952_323-945del others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(2): Show |
T | 48 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(45): Show |
48 | HG00423.hp1 HG01109.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.323-953_323-945del others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0001g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.323-954_323-945del others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(6): Show |
T | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.323-957_323-945del others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(7): Show |
T | 7 | a0001c0001t0001g0264 a0001c0001t0001g0340 a0001c0001t0001g0341 others(4): Show |
7 | HG02895.hp1 HG03098.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-958_323-945del others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(8): Show |
T | 7 | a0001c0001t0001g0297 a0002c0002t0003g0024 a0002c0002t0003g0039 others(4): Show |
7 | HG02738.hp1 HG03688.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-959_323-945del others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(9): Show |
T | 62 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(59): Show |
64 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.323-960_323-945del others(16): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(10): Show |
T | 2 | a0002c0002t0003g0075 a0002c0002t0003g0121 |
2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.323-961_323-945del others(17): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(11): Show |
T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-962_323-945del others(18): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(15): Show |
T | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.323-966_323-945del others(22): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(16): Show |
T | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323-967_323-945del others(23): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(17): Show |
T | 1 | a0001c0001t0001g0324 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.323-968_323-945del others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40617975 | TAAAAAAA others(19): Show |
T | 1 | a0003c0003t0002g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.323-970_323-945del others(26): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | ||||||
chr15:40618237 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-722A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618237 | |||||||
chr15:40618470 | C | T | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.323-489C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618470 | |||||||
chr15:40618472 | C | G | 1 | a0001c0006t0001g0230 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.323-487C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618472 | |||||||
chr15:40618509 | T | C | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.323-450T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618509 | |||||||
chr15:40618705 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-254G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618705 | |||||||
chr15:40618724 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-235A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618724 | |||||||
chr15:40618829 | C | T | 1 | a0003c0003t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.323-130C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618829 | |||||||
chr15:40619102 | A | T | 2 | a0009c0010t0001g0214 a0009c0010t0001g0215 |
2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.375+91A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619102 | |||||||
chr15:40619254 | A | G | 1 | a0002c0002t0003g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.375+243A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619254 | |||||||
chr15:40619328 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.375+317T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619328 | |||||||
chr15:40619355 | A | AAT | 127 | a0001c0001t0001g0219 a0001c0001t0001g0282 a0001c0001t0001g0309 others(124): Show |
129 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.375+365_375+366dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | ||||||
chr15:40619355 | A | AATAT | 13 | a0002c0002t0001g0090 a0002c0002t0001g0112 a0002c0002t0003g0066 others(10): Show |
13 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+363_375+366dup others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | ||||||
chr15:40619355 | A | AATATAT | 4 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(1): Show |
4 | HG02015.hp1 HG02886.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+361_375+366dup others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | ||||||
chr15:40619355 | AAT | A | 62 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(59): Show |
63 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.375+365_375+366del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | ||||||
chr15:40619376 | A | T | 1 | a0003c0003t0002g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+365A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619376 | |||||||
chr15:40619377 | T | TTAGGCTA others(3): Show |
1 | a0003c0003t0002g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+367_375+368ins others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619377 | ||||||
chr15:40619379 | T | A | 1 | a0003c0003t0002g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+368T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619379 | |||||||
chr15:40619725 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.375+714C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619725 | |||||||
chr15:40619872 | C | T | 1 | a0004c0011t0001g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376-768C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619872 | |||||||
chr15:40619902 | A | G | 4 | a0002c0002t0003g0050 a0002c0002t0003g0065 a0002c0002t0003g0069 others(1): Show |
4 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-738A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619902 | |||||||
chr15:40620188 | C | T | 1 | a0003c0003t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.376-452C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620188 | |||||||
chr15:40620216 | A | AT | 126 | a0001c0001t0001g0303 a0002c0002t0001g0026 a0002c0002t0001g0027 others(123): Show |
128 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.376-409dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40620216 | ||||||
chr15:40620216 | ATT | A | 67 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(64): Show |
68 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.376-410_376-409del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40620216 | ||||||
chr15:40620387 | T | C | 2 | a0003c0003t0002g0159 a0003c0003t0002g0164 |
2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.376-253T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620387 | |||||||
chr15:40620413 | A | G | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.376-227A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620413 | |||||||
chr15:40620505 | T | C | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.376-135T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620505 | |||||||
chr15:40620577 | T | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.376-63T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620577 | |||||||
chr15:40620618 | T | C | 1 | a0003c0003t0002g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.376-22T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620618 | |||||||
chr15:40625692 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5376+52G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40625692 | |||||||
chr15:40625931 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+291A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40625931 | |||||||
chr15:40626327 | C | CT | 34 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(31): Show |
34 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.5376+702dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40626327 | ||||||
chr15:40626350 | T | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5376+710T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626350 | |||||||
chr15:40626355 | G | A | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5376+715G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626355 | |||||||
chr15:40626386 | G | A | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5376+746G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626386 | |||||||
chr15:40626386 | G | C | 1 | a0002c0002t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5376+746G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626386 | |||||||
chr15:40626394 | C | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+754C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626394 | |||||||
chr15:40626405 | A | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+765A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626405 | |||||||
chr15:40626563 | G | A | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5376+923G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626563 | |||||||
chr15:40626563 | G | C | 3 | a0004c0004t0001g0246 a0004c0004t0001g0254 a0004c0004t0001g0256 |
3 | HG02647.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5376+923G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626563 | |||||||
chr15:40626628 | G | T | 70 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(67): Show |
72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.5376+988G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626628 | |||||||
chr15:40626648 | C | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5376+1008C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626648 | |||||||
chr15:40626649 | G | T | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5376+1009G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626649 | |||||||
chr15:40626720 | C | T | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5376+1080C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626720 | |||||||
chr15:40626747 | T | G | 24 | a0004c0004t0001g0240 a0004c0004t0001g0241 a0004c0004t0001g0242 others(21): Show |
24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.5376+1107T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626747 | |||||||
chr15:40626781 | C | T | 1 | a0002c0028t0003g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5376+1141C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626781 | |||||||
chr15:40626832 | G | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5376+1192G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626832 | |||||||
chr15:40626888 | T | C | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5377-1182T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626888 | |||||||
chr15:40627087 | G | A | 2 | a0001c0001t0001g0210 a0025c0040t0001g0211 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5377-983G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627087 | |||||||
chr15:40627095 | A | G | 1 | a0008c0009t0007g0007 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5377-975A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627095 | |||||||
chr15:40627513 | CA | C | 8 | a0002c0002t0003g0072 a0002c0022t0015g0008 a0008c0009t0006g0010 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.5377-540delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40627513 | ||||||
chr15:40627536 | CA | C | 43 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(40): Show |
43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5377-530delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40627536 | ||||||
chr15:40627858 | C | T | 1 | a0004c0004t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5377-212C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627858 | |||||||
chr15:40627946 | C | T | 290 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.5377-124C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627946 | |||||||
chr15:40628771 | A | T | 2 | a0001c0001t0001g0310 a0001c0001t0004g0296 |
2 | HG02148.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.5583+93A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628771 | |||||||
chr15:40628772 | T | A | 1 | a0005c0005t0002g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5583+94T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628772 | |||||||
chr15:40628839 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5583+161A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628839 | |||||||
chr15:40628891 | G | A | 1 | a0002c0002t0003g0129 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.5583+213G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628891 | |||||||
chr15:40629380 | AGTTTCTT others(8): Show |
A | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+14_5682+28del others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629380 | ||||||
chr15:40629471 | C | CT | 189 | a0001c0001t0001g0294 a0002c0002t0001g0025 a0002c0002t0001g0026 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.5682+116dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629471 | ||||||
chr15:40629495 | C | CT | 38 | a0001c0001t0001g0142 a0001c0001t0001g0210 a0001c0001t0001g0264 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.5682+150dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | ||||||
chr15:40629495 | C | CTT | 6 | a0001c0001t0001g0271 a0001c0001t0001g0299 a0001c0001t0001g0305 others(3): Show |
6 | HG02717.hp1 HG03492.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.5682+149_5682+150d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | ||||||
chr15:40629495 | CT | C | 14 | a0001c0001t0001g0273 a0001c0006t0001g0234 a0002c0022t0015g0008 others(11): Show |
14 | HG01516.hp2 HG01978.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5682+150delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | ||||||
chr15:40629495 | CTTTTTTT others(6): Show |
C | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.5682+138_5682+150d others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | ||||||
chr15:40629500 | T | C | 2 | a0003c0003t0002g0194 a0029c0035t0001g0266 |
2 | HG01978.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.5682+129T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629500 | |||||||
chr15:40629506 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5682+135T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629506 | |||||||
chr15:40629736 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5682+365C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629736 | |||||||
chr15:40629779 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5682+408G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629779 | |||||||
chr15:40629793 | G | A | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+422G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629793 | |||||||
chr15:40629800 | C | T | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+429C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629800 | |||||||
chr15:40629862 | A | G | 3 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0003c0003t0002g0182 |
3 | HG01346.hp1 NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.5682+491A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629862 | |||||||
chr15:40629970 | C | CT | 134 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(131): Show |
136 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.5682+604dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629970 | ||||||
chr15:40630204 | T | A | 1 | a0003c0003t0002g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5682+833T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630204 | |||||||
chr15:40630205 | T | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5682+834T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630205 | |||||||
chr15:40630326 | ATT | A | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5682+960_5682+961d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40630326 | ||||||
chr15:40630330 | T | A | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5682+959T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630330 | |||||||
chr15:40630331 | T | A | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5682+960T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630331 | |||||||
chr15:40630332 | T | A | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5682+961T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630332 | |||||||
chr15:40630468 | C | T | 1 | a0006c0007t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5682+1097C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630468 | |||||||
chr15:40630567 | A | G | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5682+1196A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630567 | |||||||
chr15:40630717 | G | C | 214 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.5682+1346G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630717 | |||||||
chr15:40630787 | A | G | 1 | a0002c0002t0003g0037 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5682+1416A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630787 | |||||||
chr15:40630899 | C | T | 1 | a0004c0004t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5682+1528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630899 | |||||||
chr15:40630917 | C | T | 1 | a0003c0003t0002g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5682+1546C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630917 | |||||||
chr15:40630975 | G | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5682+1604G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630975 | |||||||
chr15:40631141 | AAAAAT | A | 8 | a0002c0002t0003g0032 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
8 | HG02523.hp2 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.5682+1780_5682+178 others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40631141 | ||||||
chr15:40631157 | CAAGG | C | 44 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(41): Show |
44 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.5682+1790_5682+179 others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40631157 | ||||||
chr15:40631485 | A | G | 7 | a0010c0013t0001g0023 a0010c0013t0001g0101 a0010c0013t0001g0105 others(4): Show |
7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.5682+2114A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631485 | |||||||
chr15:40631561 | C | A | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5682+2190C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631561 | |||||||
chr15:40631714 | G | A | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5682+2343G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631714 | |||||||
chr15:40631740 | G | A | 6 | a0003c0003t0002g0156 a0003c0003t0002g0157 a0003c0003t0002g0162 others(3): Show |
6 | HG00639.hp2 HG00733.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+2369G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631740 | |||||||
chr15:40631898 | A | G | 1 | a0005c0005t0002g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5682+2527A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631898 | |||||||
chr15:40631914 | T | G | 70 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(67): Show |
72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.5682+2543T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631914 | |||||||
chr15:40632008 | C | CA | 11 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0312 others(8): Show |
11 | HG00280.hp2 HG02080.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.5682+2653dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632008 | ||||||
chr15:40632109 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0354 |
2 | NA19003.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5682+2738C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632109 | |||||||
chr15:40632210 | A | AC | 76 | a0001c0001t0001g0221 a0001c0001t0001g0265 a0001c0001t0001g0333 others(73): Show |
78 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.5682+2848dupC | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | ||||||
chr15:40632210 | A | ACC | 38 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0087 others(35): Show |
38 | HG00597.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.5682+2847_5682+284 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | ||||||
chr15:40632210 | A | ACCC | 18 | a0002c0002t0001g0025 a0002c0002t0001g0028 a0002c0002t0001g0088 others(15): Show |
18 | HG00423.hp1 HG01109.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.5682+2846_5682+284 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | ||||||
chr15:40632220 | A | C | 1 | a0011c0012t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5682+2849A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632220 | |||||||
chr15:40632380 | A | G | 266 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.5682+3009A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632380 | |||||||
chr15:40632589 | C | T | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+3218C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632589 | |||||||
chr15:40633005 | C | T | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+3634C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633005 | |||||||
chr15:40633016 | T | A | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5682+3645T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633016 | |||||||
chr15:40633029 | C | T | 1 | a0002c0002t0016g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5682+3658C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633029 | |||||||
chr15:40633200 | G | A | 42 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5682+3829G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633200 | |||||||
chr15:40633201 | T | C | 1 | a0002c0002t0003g0122 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5682+3830T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633201 | |||||||
chr15:40633258 | C | T | 1 | a0002c0002t0016g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5682+3887C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633258 | |||||||
chr15:40633262 | G | A | 4 | a0004c0011t0001g0238 a0004c0011t0001g0239 a0004c0011t0001g0261 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.5682+3891G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633262 | |||||||
chr15:40633310 | C | CA | 78 | a0001c0001t0001g0265 a0001c0001t0001g0329 a0001c0001t0004g0313 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.5682+3959dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | ||||||
chr15:40633310 | C | CAA | 120 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(117): Show |
121 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.5682+3958_5682+395 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | ||||||
chr15:40633310 | C | CAAA | 9 | a0002c0002t0001g0025 a0002c0002t0001g0113 a0002c0002t0001g0118 others(6): Show |
9 | HG03471.hp2 HG03831.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.5682+3957_5682+395 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | ||||||
chr15:40633443 | G | A | 3 | a0003c0003t0002g0155 a0003c0003t0002g0185 a0003c0003t0002g0194 |
3 | HG01167.hp1 HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.5682+4072G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633443 | |||||||
chr15:40633461 | T | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5682+4090T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633461 | |||||||
chr15:40633666 | A | C | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5682+4295A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633666 | |||||||
chr15:40633703 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5682+4332G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633703 | |||||||
chr15:40633738 | G | A | 74 | a0002c0002t0001g0028 a0003c0003t0002g0001 a0003c0003t0002g0147 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.5682+4367G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633738 | |||||||
chr15:40633750 | A | G | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+4379A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633750 | |||||||
chr15:40634085 | T | TTTG | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5682+4732_5682+473 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40634085 | ||||||
chr15:40634189 | C | G | 1 | a0002c0002t0001g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5682+4818C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634189 | |||||||
chr15:40634398 | C | T | 3 | a0006c0007t0001g0017 a0006c0007t0001g0029 a0006c0007t0001g0139 |
3 | HG03139.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5682+5027C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634398 | |||||||
chr15:40634423 | T | C | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+5052T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634423 | |||||||
chr15:40634426 | G | A | 1 | a0010c0013t0001g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5682+5055G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634426 | |||||||
chr15:40634456 | C | G | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.5682+5085C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634456 | |||||||
chr15:40634509 | G | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5682+5138G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634509 | |||||||
chr15:40634552 | AATTGGGA others(18): Show |
A | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5682+5182_5682+520 others(29): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634552 | |||||||
chr15:40634740 | A | G | 1 | a0003c0003t0002g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5682+5369A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634740 | |||||||
chr15:40634781 | A | G | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5682+5410A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634781 | |||||||
chr15:40634957 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5682+5586A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634957 | |||||||
chr15:40635025 | C | T | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5682+5654C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635025 | |||||||
chr15:40635050 | A | AT | 6 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0038t0001g0232 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+5695dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40635050 | ||||||
chr15:40635050 | AT | A | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.5682+5695delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40635050 | ||||||
chr15:40635288 | G | C | 7 | a0001c0001t0001g0269 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG01081.hp1 HG01106.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.5683-5624G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635288 | |||||||
chr15:40635524 | T | C | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5683-5388T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635524 | |||||||
chr15:40635553 | C | T | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5683-5359C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635553 | |||||||
chr15:40635628 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5683-5284A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635628 | |||||||
chr15:40635743 | A | G | 1 | a0018c0030t0002g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5683-5169A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635743 | |||||||
chr15:40635977 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-4935G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635977 | |||||||
chr15:40635995 | G | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-4917G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635995 | |||||||
chr15:40636012 | A | G | 2 | a0005c0005t0002g0177 a0005c0005t0002g0183 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5683-4900A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636012 | |||||||
chr15:40636127 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5683-4785C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636127 | |||||||
chr15:40636205 | G | A | 1 | a0002c0002t0001g0102 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5683-4707G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636205 | |||||||
chr15:40636415 | T | C | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-4497T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636415 | |||||||
chr15:40636458 | T | C | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5683-4454T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636458 | |||||||
chr15:40636486 | G | A | 3 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0090 |
3 | NA18955.hp2 NA18972.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.5683-4426G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636486 | |||||||
chr15:40636754 | C | A | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-4158C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636754 | |||||||
chr15:40637004 | T | A | 42 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5683-3908T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637004 | |||||||
chr15:40637037 | C | A | 1 | a0004c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5683-3875C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637037 | |||||||
chr15:40637047 | C | CT | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5683-3855dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637047 | ||||||
chr15:40637135 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5683-3777C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637135 | |||||||
chr15:40637175 | C | CT | 76 | a0001c0001t0001g0295 a0001c0006t0001g0230 a0002c0002t0001g0092 others(73): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.5683-3724dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637175 | ||||||
chr15:40637256 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-3656G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637256 | |||||||
chr15:40637323 | C | CT | 132 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(129): Show |
134 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.5683-3578dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637323 | ||||||
chr15:40637368 | G | GT | 67 | a0001c0001t0001g0272 a0001c0001t0001g0311 a0001c0001t0001g0330 others(64): Show |
69 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.5683-3532dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637368 | ||||||
chr15:40637368 | G | GTT | 60 | a0002c0002t0001g0025 a0002c0002t0001g0028 a0002c0002t0001g0087 others(57): Show |
60 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.5683-3533_5683-353 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637368 | ||||||
chr15:40637596 | G | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-3316G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637596 | |||||||
chr15:40637616 | T | C | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5683-3296T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637616 | |||||||
chr15:40637625 | A | G | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5683-3287A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637625 | |||||||
chr15:40637873 | G | GA | 12 | a0001c0001t0004g0279 a0003c0003t0002g0151 a0006c0007t0001g0017 others(9): Show |
12 | HG01123.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.5683-3029dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637873 | ||||||
chr15:40637885 | C | G | 1 | a0001c0001t0001g0303 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5683-3027C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637885 | |||||||
chr15:40638167 | G | C | 20 | a0002c0002t0003g0004 a0002c0002t0003g0039 a0002c0002t0003g0049 others(17): Show |
20 | HG00609.hp2 HG01192.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.5683-2745G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638167 | |||||||
chr15:40638250 | A | AG | 25 | a0001c0001t0001g0140 a0001c0001t0001g0217 a0001c0001t0001g0267 others(22): Show |
25 | HG00408.hp1 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.5683-2656dupG | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638250 | ||||||
chr15:40638251 | GGGGGGA | G | 119 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(116): Show |
121 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5683-2648_5683-264 others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638251 | ||||||
chr15:40638252 | GGGGGA | G | 9 | a0002c0002t0001g0090 a0002c0002t0001g0099 a0002c0002t0001g0106 others(6): Show |
9 | HG01496.hp2 HG02738.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5683-2655_5683-265 others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638252 | ||||||
chr15:40638257 | A | G | 2 | a0001c0001t0001g0354 a0003c0003t0002g0148 |
2 | HG02698.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.5683-2655A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638257 | |||||||
chr15:40638512 | G | T | 1 | a0004c0004t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5683-2400G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638512 | |||||||
chr15:40638669 | T | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-2243T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638669 | |||||||
chr15:40638670 | T | C | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5683-2242T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638670 | |||||||
chr15:40638709 | T | C | 1 | a0003c0003t0002g0198 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5683-2203T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638709 | |||||||
chr15:40638782 | C | T | 1 | a0001c0006t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5683-2130C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638782 | |||||||
chr15:40638784 | C | T | 3 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0090 |
3 | NA18955.hp2 NA18972.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.5683-2128C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638784 | |||||||
chr15:40638816 | C | CT | 12 | a0005c0005t0002g0143 a0005c0005t0002g0160 a0005c0005t0002g0161 others(9): Show |
12 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5683-2084dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638816 | ||||||
chr15:40638950 | T | C | 1 | a0003c0003t0002g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5683-1962T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638950 | |||||||
chr15:40639089 | A | G | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5683-1823A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639089 | |||||||
chr15:40639159 | C | CT | 68 | a0002c0002t0001g0124 a0002c0002t0003g0037 a0003c0003t0002g0001 others(65): Show |
69 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.5683-1740dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40639159 | ||||||
chr15:40639234 | C | T | 1 | a0005c0005t0002g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5683-1678C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639234 | |||||||
chr15:40639414 | C | T | 2 | a0007c0008t0005g0002 a0007c0008t0005g0054 |
3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5683-1498C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639414 | |||||||
chr15:40639425 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5683-1487A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639425 | |||||||
chr15:40639483 | G | A | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-1429G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639483 | |||||||
chr15:40639510 | A | G | 212 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.5683-1402A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639510 | |||||||
chr15:40639585 | CA | C | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5683-1314delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40639585 | ||||||
chr15:40639610 | A | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-1302A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639610 | |||||||
chr15:40639704 | G | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-1208G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639704 | |||||||
chr15:40639710 | G | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-1202G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639710 | |||||||
chr15:40639872 | C | T | 3 | a0008c0009t0006g0010 a0008c0009t0006g0012 a0032c0023t0006g0011 |
3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5683-1040C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639872 | |||||||
chr15:40639936 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5683-976G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639936 | |||||||
chr15:40640082 | T | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-830T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640082 | |||||||
chr15:40640085 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0330 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5683-819_5683-798d others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640085 | ||||||
chr15:40640098 | C | CT | 14 | a0001c0001t0001g0264 a0001c0001t0001g0294 a0001c0001t0001g0332 others(11): Show |
14 | HG00621.hp2 HG01978.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.5683-798dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | ||||||
chr15:40640098 | C | CTT | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-799_5683-798d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | ||||||
chr15:40640098 | CT | C | 8 | a0001c0001t0001g0312 a0002c0002t0001g0090 a0002c0002t0003g0041 others(5): Show |
8 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.5683-798delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | ||||||
chr15:40640103 | T | C | 1 | a0002c0002t0003g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5683-809T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640103 | |||||||
chr15:40640157 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-755C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640157 | |||||||
chr15:40640182 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5683-730C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640182 | |||||||
chr15:40640245 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-667C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640245 | |||||||
chr15:40640330 | A | T | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.5683-582A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640330 | |||||||
chr15:40640331 | A | G | 2 | a0003c0003t0002g0184 a0003c0003t0002g0189 |
2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.5683-581A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640331 | |||||||
chr15:40640445 | T | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-467T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640445 | |||||||
chr15:40640515 | G | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0340 a0001c0001t0001g0341 others(1): Show |
4 | NA18970.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.5683-397G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640515 | |||||||
chr15:40640731 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-181C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640731 | |||||||
chr15:40641347 | G | A | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5798+320G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641347 | |||||||
chr15:40641397 | A | T | 6 | a0003c0003t0002g0156 a0003c0003t0002g0157 a0003c0003t0002g0162 others(3): Show |
6 | HG00639.hp2 HG00733.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.5798+370A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641397 | |||||||
chr15:40641454 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5798+427G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641454 | |||||||
chr15:40641483 | G | A | 24 | a0004c0004t0001g0240 a0004c0004t0001g0241 a0004c0004t0001g0242 others(21): Show |
24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.5798+456G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641483 | |||||||
chr15:40641779 | A | T | 1 | a0008c0009t0007g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5798+752A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641779 | |||||||
chr15:40641838 | A | G | 17 | a0002c0002t0003g0004 a0002c0002t0003g0039 a0002c0002t0003g0049 others(14): Show |
17 | HG00609.hp2 HG01192.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.5798+811A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641838 | |||||||
chr15:40641842 | A | G | 1 | a0003c0003t0002g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5798+815A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641842 | |||||||
chr15:40641927 | A | ACCCCTCC others(3): Show |
1 | a0003c0003t0010g0150 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5798+900_5798+901i others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641927 | |||||||
chr15:40641928 | T | C | 1 | a0003c0003t0010g0150 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5798+901T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641928 | |||||||
chr15:40641976 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0335 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5798+949A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641976 | |||||||
chr15:40642002 | A | C | 1 | a0002c0002t0003g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5798+975A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642002 | |||||||
chr15:40642030 | G | T | 1 | a0004c0004t0001g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5798+1003G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642030 | |||||||
chr15:40642142 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5798+1115G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642142 | |||||||
chr15:40642259 | C | T | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5798+1232C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642259 | |||||||
chr15:40642291 | C | T | 28 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(25): Show |
28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.5798+1264C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642291 | |||||||
chr15:40642316 | G | A | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5798+1289G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642316 | |||||||
chr15:40642422 | C | T | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5798+1395C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642422 | |||||||
chr15:40642423 | G | A | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5798+1396G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642423 | |||||||
chr15:40642794 | A | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5798+1767A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642794 | |||||||
chr15:40642876 | C | T | 1 | a0005c0005t0002g0183 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5798+1849C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642876 | |||||||
chr15:40642880 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5798+1853G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642880 | |||||||
chr15:40642993 | C | T | 3 | a0006c0007t0001g0017 a0006c0007t0001g0029 a0006c0007t0001g0139 |
3 | HG03139.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5798+1966C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642993 | |||||||
chr15:40643165 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5799-1832T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643165 | |||||||
chr15:40643353 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5799-1644C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643353 | |||||||
chr15:40643366 | T | C | 2 | a0003c0003t0002g0149 a0003c0003t0002g0187 |
2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.5799-1631T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643366 | |||||||
chr15:40643456 | G | A | 3 | a0002c0002t0001g0106 a0002c0002t0001g0112 a0002c0002t0001g0115 |
3 | HG01496.hp2 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.5799-1541G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643456 | |||||||
chr15:40643489 | A | T | 2 | a0016c0019t0003g0063 a0016c0019t0003g0079 |
2 | NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.5799-1508A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643489 | |||||||
chr15:40643515 | C | T | 134 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(131): Show |
136 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.5799-1482C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643515 | |||||||
chr15:40643517 | C | T | 3 | a0002c0002t0001g0106 a0002c0002t0001g0112 a0002c0002t0001g0115 |
3 | HG01496.hp2 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.5799-1480C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643517 | |||||||
chr15:40643519 | C | G | 1 | a0002c0002t0008g0013 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.5799-1478C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643519 | |||||||
chr15:40643646 | C | T | 2 | a0017c0034t0013g0015 a0024c0033t0017g0146 |
2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5799-1351C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643646 | |||||||
chr15:40643824 | A | G | 42 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5799-1173A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643824 | |||||||
chr15:40644390 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0351 |
2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.5799-607C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644390 | |||||||
chr15:40644408 | A | G | 290 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.5799-589A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644408 | |||||||
chr15:40644470 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5799-527C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644470 | |||||||
chr15:40644614 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5799-383C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644614 | |||||||
chr15:40644646 | C | T | 3 | a0008c0009t0006g0010 a0008c0009t0006g0012 a0032c0023t0006g0011 |
3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5799-351C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644646 | |||||||
chr15:40644655 | T | C | 15 | a0002c0002t0003g0016 a0002c0002t0003g0032 a0002c0002t0003g0040 others(12): Show |
15 | HG02027.hp1 HG02523.hp2 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.5799-342T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644655 | |||||||
chr15:40644810 | T | G | 2 | a0003c0003t0002g0184 a0003c0003t0002g0189 |
2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.5799-187T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644810 | |||||||
chr15:40644914 | C | T | 2 | a0011c0012t0001g0127 a0011c0012t0001g0128 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5799-83C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644914 | |||||||
chr15:40644917 | CT | C | 41 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.5799-77delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr15 | 40644917 | ||||||
chr15:40644984 | T | C | 1 | a0001c0006t0001g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5799-13T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644984 | |||||||
chr15:40645139 | T | C | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5889+52T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645139 | |||||||
chr15:40645214 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5889+127G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645214 | |||||||
chr15:40645377 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5890-279G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645377 | |||||||
chr15:40645384 | T | C | 2 | a0011c0012t0001g0127 a0011c0012t0001g0128 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5890-272T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645384 | |||||||
chr15:40645444 | C | G | 1 | a0001c0001t0004g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5890-212C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645444 | |||||||
chr15:40645449 | A | G | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5890-207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645449 | |||||||
chr15:40645529 | C | T | 351 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(348): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.5890-127C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645529 | |||||||
chr15:40645603 | C | T | 1 | a0003c0003t0002g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5890-53C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645603 | |||||||
chr15:40645615 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5890-41G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645615 | |||||||
chr15:40645796 | TAGAA | T | 11 | a0005c0005t0002g0143 a0005c0005t0002g0160 a0005c0005t0002g0161 others(8): Show |
11 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6006+28_6006+31del others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40645796 | ||||||
chr15:40645841 | A | T | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6006+69A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645841 | |||||||
chr15:40645938 | C | T | 3 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 |
3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.6006+166C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645938 | |||||||
chr15:40645979 | A | G | 1 | a0001c0001t0004g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6006+207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645979 | |||||||
chr15:40646141 | G | A | 1 | a0004c0004t0001g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6006+369G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646141 | |||||||
chr15:40646347 | A | G | 1 | a0001c0038t0001g0232 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.6006+575A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646347 | |||||||
chr15:40646646 | G | A | 8 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(5): Show |
8 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.6007-341G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646646 | |||||||
chr15:40646685 | A | G | 1 | a0001c0006t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6007-302A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646685 | |||||||
chr15:40646714 | A | T | 2 | a0002c0002t0001g0135 a0002c0025t0001g0136 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6007-273A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646714 | |||||||
chr15:40646718 | A | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6007-269A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646718 | |||||||
chr15:40646725 | C | T | 1 | a0006c0007t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6007-262C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646725 | |||||||
chr15:40646856 | C | CA | 24 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0012g0220 others(21): Show |
24 | HG00609.hp2 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.6007-109dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40646856 | ||||||
chr15:40646856 | CA | C | 15 | a0001c0001t0001g0269 a0001c0001t0001g0305 a0001c0001t0001g0341 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.6007-109delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40646856 | ||||||
chr15:40646896 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6007-91T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646896 | |||||||
chr15:40646920 | A | G | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6007-67A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646920 | |||||||
chr15:40647155 | C | T | 1 | a0002c0002t0003g0137 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.6094+81C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647155 | |||||||
chr15:40647213 | G | A | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6094+139G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647213 | |||||||
chr15:40647250 | G | A | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.6094+176G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647250 | |||||||
chr15:40647454 | G | A | 238 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.6094+380G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647454 | |||||||
chr15:40647489 | A | T | 1 | a0002c0002t0003g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6094+415A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647489 | |||||||
chr15:40647515 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6094+441C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647515 | |||||||
chr15:40647528 | C | T | 1 | a0002c0025t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6094+454C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647528 | |||||||
chr15:40647628 | C | T | 1 | a0004c0004t0001g0256 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6094+554C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647628 | |||||||
chr15:40647769 | G | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6094+695G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647769 | |||||||
chr15:40647915 | T | G | 2 | a0002c0002t0003g0048 a0002c0002t0003g0064 |
2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.6094+841T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647915 | |||||||
chr15:40647950 | A | G | 71 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(68): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.6094+876A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647950 | |||||||
chr15:40648041 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.6094+967G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648041 | |||||||
chr15:40648077 | TAA | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6094+1007_6094+100 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648077 | ||||||
chr15:40648244 | G | A | 4 | a0001c0001t0001g0264 a0001c0001t0001g0340 a0001c0001t0001g0341 others(1): Show |
4 | NA18970.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.6094+1170G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648244 | |||||||
chr15:40648442 | AT | A | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6094+1369delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648442 | |||||||
chr15:40648495 | T | G | 1 | a0006c0007t0001g0017 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6094+1421T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648495 | |||||||
chr15:40648508 | G | T | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6094+1434G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648508 | |||||||
chr15:40648611 | G | A | 1 | a0004c0004t0001g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6094+1537G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648611 | |||||||
chr15:40648829 | CT | C | 202 | a0001c0001t0001g0210 a0001c0001t0001g0271 a0001c0001t0001g0284 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.6095-1454delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648829 | ||||||
chr15:40648843 | T | G | 1 | a0002c0002t0003g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6095-1458T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648843 | |||||||
chr15:40648864 | G | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.6095-1437G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648864 | |||||||
chr15:40648869 | TACCCAGG others(9): Show |
T | 1 | a0001c0001t0001g0331 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1430_6095-141 others(20): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648869 | ||||||
chr15:40648888 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1413G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648888 | |||||||
chr15:40648889 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1412G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648889 | |||||||
chr15:40648916 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.6095-1385G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648916 | |||||||
chr15:40648964 | G | A | 1 | a0001c0006t0001g0230 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6095-1337G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648964 | |||||||
chr15:40648970 | C | T | 1 | a0005c0005t0002g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6095-1331C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648970 | |||||||
chr15:40648988 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6095-1313C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648988 | |||||||
chr15:40648996 | A | AT | 128 | a0001c0001t0001g0269 a0001c0001t0001g0301 a0001c0001t0001g0302 others(125): Show |
130 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.6095-1292dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648996 | ||||||
chr15:40648996 | A | ATT | 11 | a0002c0002t0001g0124 a0002c0002t0003g0046 a0006c0007t0001g0017 others(8): Show |
11 | HG01256.hp2 HG02895.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.6095-1293_6095-129 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648996 | ||||||
chr15:40649044 | G | A | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6095-1257G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649044 | |||||||
chr15:40649115 | G | T | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6095-1186G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649115 | |||||||
chr15:40649130 | G | A | 3 | a0004c0004t0001g0246 a0004c0004t0001g0254 a0004c0004t0001g0256 |
3 | HG02647.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6095-1171G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649130 | |||||||
chr15:40649180 | A | G | 4 | a0002c0002t0001g0088 a0002c0002t0001g0094 a0002c0002t0001g0104 others(1): Show |
4 | HG01168.hp2 HG02293.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.6095-1121A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649180 | |||||||
chr15:40649197 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6095-1104T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649197 | |||||||
chr15:40649549 | C | T | 1 | a0001c0006t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6095-752C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649549 | |||||||
chr15:40649616 | A | G | 2 | a0002c0002t0003g0046 a0002c0002t0003g0131 |
2 | NA18962.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.6095-685A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649616 | |||||||
chr15:40649700 | G | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6095-601G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649700 | |||||||
chr15:40649762 | C | T | 12 | a0002c0002t0003g0004 a0002c0002t0003g0039 a0002c0002t0003g0051 others(9): Show |
12 | HG01192.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.6095-539C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649762 | |||||||
chr15:40649811 | C | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6095-490C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649811 | |||||||
chr15:40650125 | GA | G | 45 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(42): Show |
45 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.6095-161delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40650125 | ||||||
chr15:40650517 | G | GT | 13 | a0001c0001t0001g0280 a0001c0001t0004g0279 a0001c0001t0012g0220 others(10): Show |
13 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.6173-13dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr15 | 40650517 | ||||||
chr15:40650517 | GT | G | 102 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(99): Show |
104 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.6173-13delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr15 | 40650517 | ||||||
chr15:40650588 | G | A | 2 | a0005c0005t0002g0179 a0005c0005t0002g0201 |
2 | HG02965.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.6212+5G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650588 | |||||||
chr15:40650852 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.6212+269A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650852 | |||||||
chr15:40650922 | A | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6212+339A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650922 | |||||||
chr15:40651075 | C | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6213-396C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651075 | |||||||
chr15:40651075 | C | CA | 15 | a0001c0001t0001g0264 a0001c0001t0004g0316 a0001c0038t0001g0232 others(12): Show |
15 | HG00099.hp2 HG01109.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.6213-383dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651075 | ||||||
chr15:40651124 | A | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6213-347A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651124 | |||||||
chr15:40651290 | TTA | T | 67 | a0002c0002t0001g0087 a0002c0002t0001g0110 a0002c0002t0001g0124 others(64): Show |
68 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.6213-176_6213-175d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651290 | ||||||
chr15:40651292 | A | T | 1 | a0004c0004t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6213-179A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651292 | |||||||
chr15:40651293 | TATA | T | 71 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(68): Show |
71 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.6213-176_6213-174d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651293 | ||||||
chr15:40651293 | TATAA | T | 69 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(66): Show |
71 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.6213-176_6213-173d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651293 | ||||||
chr15:40651295 | T | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6213-176T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651295 | |||||||
chr15:40651295 | TA | T | 12 | a0001c0001t0001g0271 a0001c0001t0001g0305 a0001c0001t0001g0327 others(9): Show |
12 | HG01928.hp2 NA18951.hp2 NA18962.hp2 others(9): Show |
intron_variant | MODIFIER | c.6213-159delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651295 | ||||||
chr15:40651413 | A | C | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6213-58A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651413 | |||||||
chr15:40651905 | C | T | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6315-100C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651905 | |||||||
chr15:40651906 | A | T | 1 | a0004c0004t0001g0256 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6315-99A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651906 | |||||||
chr15:40651945 | A | T | 1 | a0002c0002t0003g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6315-60A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651945 | |||||||
chr15:40652133 | T | A | 1 | a0002c0002t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6415+28T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652133 | |||||||
chr15:40652186 | A | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6415+81A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652186 | |||||||
chr15:40652196 | C | T | 3 | a0011c0012t0001g0031 a0011c0012t0001g0127 a0011c0012t0001g0128 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6415+91C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652196 | |||||||
chr15:40652211 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6415+106G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652211 | |||||||
chr15:40652250 | A | G | 2 | a0001c0001t0001g0210 a0025c0040t0001g0211 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6415+145A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652250 | |||||||
chr15:40652455 | CT | C | 202 | a0001c0001t0001g0286 a0002c0002t0001g0025 a0002c0002t0001g0026 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.6415+367delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652455 | ||||||
chr15:40652455 | CTT | C | 8 | a0002c0002t0001g0094 a0002c0002t0003g0024 a0002c0002t0003g0057 others(5): Show |
8 | HG01109.hp2 HG01168.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.6415+366_6415+367d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652455 | ||||||
chr15:40652508 | G | A | 1 | a0015c0017t0003g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6415+403G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652508 | |||||||
chr15:40652583 | C | A | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6415+478C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652583 | |||||||
chr15:40652583 | C | T | 9 | a0001c0001t0001g0280 a0001c0001t0001g0291 a0001c0001t0001g0308 others(6): Show |
9 | HG00621.hp1 HG02056.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.6415+478C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652583 | |||||||
chr15:40652750 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6415+645A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652750 | |||||||
chr15:40652753 | A | ACT | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6415+649_6415+650d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652753 | ||||||
chr15:40652760 | C | CAA | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.6415+672_6415+673d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652760 | ||||||
chr15:40652760 | C | CAAA | 78 | a0002c0002t0001g0089 a0002c0002t0001g0090 a0002c0002t0001g0113 others(75): Show |
80 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.6415+671_6415+673d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652760 | ||||||
chr15:40652771 | A | G | 1 | a0004c0004t0001g0245 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6415+666A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652771 | |||||||
chr15:40652791 | A | T | 1 | a0001c0001t0001g0286 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6415+686A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652791 | |||||||
chr15:40652861 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+756G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652861 | |||||||
chr15:40653071 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+966G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653071 | |||||||
chr15:40653073 | G | A | 2 | a0015c0017t0003g0044 a0015c0017t0003g0067 |
2 | HG02293.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.6415+968G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653073 | |||||||
chr15:40653205 | T | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+1100T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653205 | |||||||
chr15:40653350 | G | T | 2 | a0011c0012t0001g0127 a0011c0012t0001g0128 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6415+1245G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653350 | |||||||
chr15:40653547 | T | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6416-1362T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653547 | |||||||
chr15:40653701 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6416-1208G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653701 | |||||||
chr15:40653702 | T | C | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6416-1207T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653702 | |||||||
chr15:40653760 | G | A | 1 | a0033c0042t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6416-1149G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653760 | |||||||
chr15:40653862 | C | A | 1 | a0001c0001t0004g0315 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6416-1047C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653862 | |||||||
chr15:40653864 | C | T | 1 | a0008c0009t0007g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6416-1045C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653864 | |||||||
chr15:40653868 | C | T | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6416-1041C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653868 | |||||||
chr15:40653872 | GT | G | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6416-1033delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40653872 | ||||||
chr15:40654003 | G | A | 2 | a0002c0002t0001g0092 a0002c0002t0001g0093 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6416-906G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654003 | |||||||
chr15:40654036 | T | G | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6416-873T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654036 | |||||||
chr15:40654095 | T | A | 71 | a0002c0002t0003g0003 a0002c0002t0003g0004 a0002c0002t0003g0014 others(68): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.6416-814T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654095 | |||||||
chr15:40654249 | T | G | 1 | a0002c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6416-660T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654249 | |||||||
chr15:40654423 | GTAGTTGA others(6): Show |
G | 11 | a0005c0005t0002g0143 a0005c0005t0002g0160 a0005c0005t0002g0161 others(8): Show |
11 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6416-484_6416-472d others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654423 | ||||||
chr15:40654573 | T | TA | 9 | a0001c0001t0001g0217 a0001c0001t0001g0303 a0002c0002t0001g0090 others(6): Show |
9 | HG01256.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.6416-322dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | ||||||
chr15:40654573 | T | TAA | 65 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(62): Show |
66 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.6416-323_6416-322d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | ||||||
chr15:40654573 | T | TAAA | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6416-324_6416-322d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | ||||||
chr15:40654597 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0275 |
2 | HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.6416-312C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654597 | |||||||
chr15:40654706 | A | G | 3 | a0002c0002t0003g0083 a0013c0016t0003g0036 a0013c0016t0003g0125 |
3 | HG00544.hp2 NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.6416-203A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654706 | |||||||
chr15:40654730 | G | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6416-179G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654730 | |||||||
chr15:40654825 | C | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6416-84C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654825 | |||||||
chr15:40654833 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.6416-76C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654833 | |||||||
chr15:40654856 | G | A | 1 | a0002c0022t0015g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6416-53G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654856 | |||||||
chr15:40655126 | C | T | 2 | a0007c0008t0005g0002 a0007c0008t0005g0054 |
3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.6484+149C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655126 | |||||||
chr15:40655188 | C | T | 1 | a0020c0041t0001g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6484+211C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655188 | |||||||
chr15:40655210 | A | G | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+233A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655210 | |||||||
chr15:40655230 | G | A | 1 | a0001c0006t0001g0231 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6484+253G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655230 | |||||||
chr15:40655288 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0281 a0001c0001t0001g0334 |
3 | NA18946.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.6484+311C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655288 | |||||||
chr15:40655505 | C | T | 358 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(355): Show |
363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.6484+528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655505 | |||||||
chr15:40655540 | G | A | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+563G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655540 | |||||||
chr15:40655590 | C | CA | 7 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0297 others(4): Show |
7 | HG03098.hp1 HG03453.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.6484+634dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | ||||||
chr15:40655590 | CAA | C | 73 | a0002c0002t0003g0074 a0003c0003t0002g0001 a0003c0003t0002g0147 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6484+633_6484+634d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | ||||||
chr15:40655590 | CAAAA | C | 130 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(127): Show |
132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.6484+631_6484+634d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | ||||||
chr15:40655636 | C | T | 4 | a0002c0002t0003g0014 a0002c0002t0003g0048 a0002c0002t0003g0061 others(1): Show |
4 | HG01074.hp1 HG02486.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.6484+659C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655636 | |||||||
chr15:40655915 | C | CA | 11 | a0001c0006t0001g0227 a0002c0002t0001g0090 a0002c0002t0001g0113 others(8): Show |
11 | HG02055.hp2 HG02293.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.6484+955dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655915 | ||||||
chr15:40655915 | CA | C | 6 | a0001c0001t0001g0336 a0002c0002t0003g0055 a0002c0002t0003g0083 others(3): Show |
6 | HG01975.hp2 HG02572.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.6484+955delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655915 | ||||||
chr15:40656006 | G | A | 2 | a0005c0005t0002g0179 a0005c0005t0002g0201 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6484+1029G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656006 | |||||||
chr15:40656006 | G | C | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+1029G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656006 | |||||||
chr15:40656055 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0312 a0024c0033t0017g0146 |
3 | HG02040.hp1 HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.6485-987C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656055 | |||||||
chr15:40656293 | C | CATTGTGG others(30): Show |
1 | a0001c0001t0001g0297 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.6485-730_6485-729i others(39): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40656293 | ||||||
chr15:40656346 | T | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6485-696T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656346 | |||||||
chr15:40656444 | T | C | 1 | a0005c0005t0002g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6485-598T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656444 | |||||||
chr15:40656688 | G | C | 210 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.6485-354G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656688 | |||||||
chr15:40656733 | A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-309A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656733 | |||||||
chr15:40656734 | A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-308A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656734 | |||||||
chr15:40656735 | A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-307A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656735 | |||||||
chr15:40656736 | A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-306A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656736 | |||||||
chr15:40656743 | G | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-299G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656743 | |||||||
chr15:40656745 | G | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-297G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656745 | |||||||
chr15:40656749 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-293G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656749 | |||||||
chr15:40656750 | G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-292G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656750 | |||||||
chr15:40656758 | C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-284C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656758 | |||||||
chr15:40656759 | G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-283G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656759 | |||||||
chr15:40656771 | A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-271A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656771 | |||||||
chr15:40656773 | C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-269C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656773 | |||||||
chr15:40656775 | A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-267A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656775 | |||||||
chr15:40656776 | C | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-266C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656776 | |||||||
chr15:40656777 | T | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-265T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656777 | |||||||
chr15:40656785 | C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-257C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656785 | |||||||
chr15:40656786 | T | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-256T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656786 | |||||||
chr15:40656787 | G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-255G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656787 | |||||||
chr15:40656789 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-253G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656789 | |||||||
chr15:40656790 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-252G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656790 | |||||||
chr15:40656794 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-248G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656794 | |||||||
chr15:40656801 | G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-241G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656801 | |||||||
chr15:40656803 | T | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-239T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656803 | |||||||
chr15:40656804 | T | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-238T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656804 | |||||||
chr15:40656805 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-237G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656805 | |||||||
chr15:40656808 | C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-234C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656808 | |||||||
chr15:40656812 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-230G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656812 | |||||||
chr15:40656813 | A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-229A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656813 | |||||||
chr15:40656817 | C | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-225C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656817 | |||||||
chr15:40656824 | T | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-218T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656824 | |||||||
chr15:40656825 | G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-217G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656825 | |||||||
chr15:40656826 | C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-216C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656826 | |||||||
chr15:40656843 | G | A | 1 | a0002c0002t0003g0083 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6485-199G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656843 | |||||||
chr15:40656850 | T | C | 2 | a0005c0005t0002g0160 a0005c0005t0002g0166 |
2 | HG01255.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6485-192T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656850 | |||||||
chr15:40657303 | G | A | 1 | a0008c0009t0006g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6595-52G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 23/25 | chr15 | 40657303 | |||||||
chr15:40657328 | C | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6595-27C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 23/25 | chr15 | 40657328 | |||||||
chr15:40657596 | G | T | 1 | a0001c0001t0001g0326 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.6713+123G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657596 | |||||||
chr15:40657705 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6713+232G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657705 | |||||||
chr15:40657903 | G | T | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6713+430G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657903 | |||||||
chr15:40657957 | T | C | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6713+484T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657957 | |||||||
chr15:40657965 | T | A | 213 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.6713+492T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657965 | |||||||
chr15:40658177 | A | G | 16 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0001g0299 others(13): Show |
16 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.6713+704A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658177 | |||||||
chr15:40658247 | A | G | 2 | a0015c0017t0003g0044 a0015c0017t0003g0067 |
2 | HG02293.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.6713+774A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658247 | |||||||
chr15:40658269 | C | T | 1 | a0002c0002t0001g0090 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6713+796C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658269 | |||||||
chr15:40658290 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6713+817G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658290 | |||||||
chr15:40658335 | C | T | 2 | a0003c0003t0002g0173 a0003c0003t0002g0174 |
2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6713+862C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658335 | |||||||
chr15:40658375 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0335 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.6713+902A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658375 | |||||||
chr15:40658485 | C | T | 1 | a0002c0002t0003g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6714-854C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658485 | |||||||
chr15:40658523 | ATCTCAAA others(27): Show |
A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0343 |
2 | HG00423.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.6714-793_6714-760d others(36): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658523 | ||||||
chr15:40658527 | C | CA | 9 | a0001c0001t0001g0338 a0001c0001t0001g0354 a0003c0003t0002g0182 others(6): Show |
9 | HG01346.hp1 HG02056.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.6714-793dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658527 | ||||||
chr15:40658527 | CA | C | 7 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0276 others(4): Show |
7 | HG01256.hp2 HG01516.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6714-793delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658527 | ||||||
chr15:40658544 | AAAG | A | 130 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(127): Show |
130 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.6714-793_6714-791d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658544 | ||||||
chr15:40658561 | CA | C | 202 | a0001c0001t0001g0269 a0001c0001t0001g0281 a0001c0001t0001g0317 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.6714-760delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658561 | ||||||
chr15:40658561 | CAA | C | 15 | a0002c0002t0003g0130 a0004c0004t0001g0249 a0005c0005t0002g0143 others(12): Show |
15 | HG00639.hp1 HG01255.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.6714-761_6714-760d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658561 | ||||||
chr15:40658576 | A | G | 35 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 others(32): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.6714-763A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658576 | |||||||
chr15:40658590 | A | C | 1 | a0024c0033t0017g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6714-749A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658590 | |||||||
chr15:40658711 | C | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6714-628C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658711 | |||||||
chr15:40658788 | G | T | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6714-551G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658788 | |||||||
chr15:40658929 | C | CA | 7 | a0001c0001t0001g0271 a0001c0001t0001g0305 a0001c0001t0001g0327 others(4): Show |
7 | HG00741.hp1 NA18951.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.6714-397dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658929 | ||||||
chr15:40658939 | A | AAAAG | 131 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(128): Show |
133 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.6714-396_6714-393d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658939 | ||||||
chr15:40658982 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6714-357C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658982 | |||||||
chr15:40659017 | G | A | 3 | a0008c0009t0006g0010 a0008c0009t0006g0012 a0032c0023t0006g0011 |
3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6714-322G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659017 | |||||||
chr15:40659061 | C | A | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6714-278C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659061 | |||||||
chr15:40659241 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6714-98G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659241 | |||||||
chr15:40659482 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6836+21G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659482 | |||||||
chr15:40659630 | C | A | 1 | a0007c0008t0005g0053 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6836+169C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659630 | |||||||
chr15:40659892 | T | TTGTGTGT others(3): Show |
25 | a0003c0003t0002g0149 a0003c0003t0002g0156 a0003c0003t0002g0157 others(22): Show |
25 | HG00733.hp2 HG01123.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | ||||||
chr15:40659892 | T | TTGTGTGT others(5): Show |
7 | a0003c0003t0002g0152 a0003c0003t0002g0155 a0003c0003t0002g0162 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | ||||||
chr15:40659892 | T | TTGTGTGT others(7): Show |
27 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0151 others(24): Show |
28 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(16): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | ||||||
chr15:40659892 | T | TTGTGTGT others(9): Show |
6 | a0003c0003t0002g0159 a0003c0003t0002g0164 a0003c0003t0002g0168 others(3): Show |
6 | HG02735.hp1 HG02895.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(18): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | ||||||
chr15:40659892 | T | TTGTGTGT others(15): Show |
3 | a0003c0003t0002g0180 a0003c0003t0002g0195 a0003c0003t0014g0188 |
3 | HG00408.hp2 HG02056.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.6836+432_6836+433i others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | ||||||
chr15:40659894 | A | ATG | 30 | a0001c0001t0001g0269 a0001c0001t0001g0274 a0001c0001t0001g0276 others(27): Show |
30 | HG00423.hp2 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.6836+465_6836+466d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | ATGTG | 40 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(37): Show |
40 | HG00423.hp1 HG00673.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.6836+463_6836+466d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | ATGTGTG | 52 | a0002c0002t0001g0113 a0002c0002t0001g0120 a0002c0002t0003g0003 others(49): Show |
53 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.6836+461_6836+466d others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | ATGTGTGT others(1): Show |
12 | a0002c0002t0001g0089 a0002c0002t0003g0034 a0002c0002t0003g0040 others(9): Show |
12 | HG00639.hp1 HG00642.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.6836+459_6836+466d others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | ATGTGTGT others(3): Show |
15 | a0002c0002t0003g0042 a0002c0002t0003g0050 a0002c0002t0003g0062 others(12): Show |
16 | HG00099.hp2 HG00738.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.6836+457_6836+466d others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | ATGTGTGT others(5): Show |
7 | a0002c0002t0001g0126 a0002c0002t0003g0080 a0006c0007t0001g0017 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.6836+455_6836+466d others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | ||||||
chr15:40659894 | A | G | 73 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6836+433A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659894 | |||||||
chr15:40659927 | T | TGTGTGTG others(4): Show |
1 | a0007c0008t0005g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6836+466_6836+467i others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | |||||||
chr15:40659927 | T | TGTGTGTG others(8): Show |
1 | a0003c0003t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6836+466_6836+467i others(17): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | |||||||
chr15:40659927 | T | TGTGTGTG others(10): Show |
2 | a0005c0005t0002g0144 a0005c0015t0002g0145 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6836+466_6836+467i others(19): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | |||||||
chr15:40659948 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6836+487G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659948 | |||||||
chr15:40660063 | C | T | 32 | a0002c0002t0003g0003 a0002c0002t0003g0014 a0002c0002t0003g0022 others(29): Show |
34 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.6836+602C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660063 | |||||||
chr15:40660100 | T | G | 1 | a0002c0002t0003g0083 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6836+639T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660100 | |||||||
chr15:40660122 | A | G | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6836+661A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660122 | |||||||
chr15:40660392 | C | T | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6836+931C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660392 | |||||||
chr15:40660464 | A | T | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1003A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660464 | |||||||
chr15:40660506 | A | T | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1045A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660506 | |||||||
chr15:40660508 | T | C | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1047T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660508 | |||||||
chr15:40660510 | C | A | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1049C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660510 | |||||||
chr15:40660664 | C | CA | 260 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0216 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.6836+1224dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40660664 | ||||||
chr15:40660664 | C | CAA | 29 | a0001c0001t0001g0221 a0001c0001t0012g0220 a0002c0002t0001g0087 others(26): Show |
29 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.6836+1223_6836+122 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40660664 | ||||||
chr15:40660793 | T | C | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-1281T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660793 | |||||||
chr15:40660871 | G | A | 1 | a0002c0002t0003g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6837-1203G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660871 | |||||||
chr15:40660886 | C | G | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-1188C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660886 | |||||||
chr15:40660987 | G | A | 66 | a0003c0003t0002g0001 a0003c0003t0002g0147 a0003c0003t0002g0148 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6837-1087G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660987 | |||||||
chr15:40661038 | T | C | 4 | a0004c0004t0001g0355 a0004c0004t0001g0356 a0004c0004t0001g0357 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.6837-1036T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661038 | |||||||
chr15:40661086 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-988C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661086 | |||||||
chr15:40661095 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6837-979C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661095 | |||||||
chr15:40661127 | A | T | 4 | a0009c0010t0001g0213 a0009c0010t0001g0214 a0009c0010t0001g0215 others(1): Show |
4 | NA18950.hp2 NA18983.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.6837-947A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661127 | |||||||
chr15:40661129 | T | A | 1 | a0001c0001t0001g0317 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.6837-945T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661129 | |||||||
chr15:40661165 | T | G | 135 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.6837-909T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661165 | |||||||
chr15:40661218 | C | T | 3 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6837-856C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661218 | |||||||
chr15:40661259 | G | A | 4 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0002t0001g0111 others(1): Show |
4 | HG00423.hp1 HG02155.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.6837-815G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661259 | |||||||
chr15:40661293 | C | CCATCCTG others(78): Show |
1 | a0002c0002t0016g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-773_6837-772i others(87): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40661293 | ||||||
chr15:40661327 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-747C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661327 | |||||||
chr15:40661352 | C | G | 1 | a0002c0002t0016g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-722C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661352 | |||||||
chr15:40661352 | C | T | 7 | a0005c0005t0002g0205 a0005c0005t0002g0206 a0005c0005t0002g0208 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-722C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661352 | |||||||
chr15:40661353 | G | C | 1 | a0002c0002t0016g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-721G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661353 | |||||||
chr15:40661363 | G | C | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6837-711G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661363 | |||||||
chr15:40661380 | T | C | 1 | a0002c0002t0003g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6837-694T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661380 | |||||||
chr15:40661387 | G | A | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-687G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661387 | |||||||
chr15:40661388 | A | G | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-686A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661388 | |||||||
chr15:40661452 | A | G | 42 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.6837-622A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661452 | |||||||
chr15:40661770 | C | T | 129 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(126): Show |
131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.6837-304C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661770 | |||||||
chr15:40661809 | G | C | 38 | a0002c0002t0001g0025 a0002c0002t0001g0087 a0002c0002t0001g0088 others(35): Show |
38 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.6837-265G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661809 | |||||||
chr15:40661844 | C | T | 1 | a0018c0030t0002g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.6837-230C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661844 | |||||||
chr15:40661852 | G | C | 6 | a0002c0022t0015g0008 a0008c0009t0006g0010 a0008c0009t0006g0012 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6837-222G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661852 | |||||||
chr15:40661903 | T | G | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-171T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661903 | |||||||
chr15:40661904 | G | T | 1 | a0002c0002t0003g0074 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-170G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661904 | |||||||
chr15:40661944 | G | A | 1 | a0017c0034t0013g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6837-130G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661944 |