Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 988 |
| ensemblid | ENSG00000096401.8 |
| hgncid | 1743 |
| symbol | CDC5L |
| name | cell division cycle 5 like |
| refseq_nuc | NM_001253.4 |
| refseq_prot | NP_001244.1 |
| ensembl_nuc | ENST00000371477.4 |
| ensembl_prot | ENSP00000360532.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 44387706 |
| end | 44450425 |
| strand | + |
| ver | v1.2 |
| region | chr6:44387706-44450425 |
| region5000 | chr6:44382706-44455425 |
| regionname0 | CDC5L_chr6_44387706_44450425 |
| regionname5000 | CDC5L_chr6_44382706_44455425 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 802 | 351 | 83 | 54 | 176 | 8 | 28 | 142 | CDC5L_chr6_44382706_44455425 | CDC5L | MPRIM others(797): Show |
chr6 | 44382706 | 44455425 |
| a0002 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | MPRIM others(797): Show |
chr6 | 44382706 | 44455425 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2406 | 166 | 52 | 30 | 65 | 5 | 12 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0002 | 0/0 | 2406 | 92 | 1 | 8 | 70 | 1 | 12 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0003 | 0/0 | 2406 | 43 | 3 | 14 | 21 | 2 | 3 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0004 | 0/0 | 2406 | 30 | 14 | 0 | 15 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0005 | 0/0 | 2406 | 8 | 6 | 2 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0006 | 0/0 | 2406 | 3 | 3 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0007 | 0/0 | 2406 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0008 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0009 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0010 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0011 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0012 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0013 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0001c0014 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 | ||
| a0002c0015 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | ATGCC others(2401): Show |
chr6 | 44382706 | 44455425 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6241 | 124 | 38 | 23 | 47 | 3 | 11 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0003 | 0/0 | 6230 | 3 | 0 | 2 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6225): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0005 | 0/0 | 6241 | 7 | 7 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0006 | 0/0 | 6238 | 9 | 1 | 0 | 8 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6233): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0008 | 0/0 | 6239 | 6 | 0 | 1 | 5 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6234): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0013 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6235): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0014 | 0/0 | 6242 | 2 | 0 | 1 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6237): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0016 | 0/0 | 6239 | 2 | 1 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6234): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0017 | 0/0 | 6241 | 2 | 2 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0018 | 0/0 | 6241 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0020 | 0/0 | 6241 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0023 | 0/0 | 6241 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0024 | 0/0 | 6241 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0025 | 0/0 | 6241 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0026 | 0/0 | 6239 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6234): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0030 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6227): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0034 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6235): Show |
chr6 | 44382706 | 44455425 |
| a0001c0001t0035 | 0/0 | 6241 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0002 | 0/0 | 6237 | 77 | 0 | 7 | 61 | 1 | 8 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0004 | 0/0 | 6231 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6226): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0005 | 0/0 | 6241 | 5 | 0 | 0 | 1 | 0 | 4 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0011 | 0/0 | 6236 | 3 | 0 | 1 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6231): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0015 | 0/0 | 6237 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0021 | 0/0 | 6236 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6231): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0027 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0002t0029 | 0/0 | 6230 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6225): Show |
chr6 | 44382706 | 44455425 |
| a0001c0003t0003 | 0/0 | 6230 | 40 | 0 | 14 | 21 | 2 | 3 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6225): Show |
chr6 | 44382706 | 44455425 |
| a0001c0003t0010 | 0/0 | 6242 | 3 | 3 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6237): Show |
chr6 | 44382706 | 44455425 |
| a0001c0004t0004 | 0/0 | 6231 | 13 | 0 | 0 | 13 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6226): Show |
chr6 | 44382706 | 44455425 |
| a0001c0004t0007 | 0/0 | 6237 | 8 | 8 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0004t0009 | 0/0 | 6239 | 6 | 5 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6234): Show |
chr6 | 44382706 | 44455425 |
| a0001c0004t0019 | 0/0 | 6241 | 2 | 0 | 0 | 1 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0004t0028 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0005t0002 | 0/0 | 6237 | 7 | 5 | 2 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0005t0031 | 0/0 | 6241 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0006t0012 | 0/0 | 6241 | 3 | 3 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0007t0002 | 0/0 | 6237 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0008t0022 | 0/0 | 6235 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6230): Show |
chr6 | 44382706 | 44455425 |
| a0001c0009t0001 | 0/0 | 6241 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0010t0033 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6235): Show |
chr6 | 44382706 | 44455425 |
| a0001c0011t0002 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0012t0002 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6232): Show |
chr6 | 44382706 | 44455425 |
| a0001c0013t0032 | 0/0 | 6241 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0001c0014t0001 | 0/0 | 6241 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6236): Show |
chr6 | 44382706 | 44455425 |
| a0002c0015t0013 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | CTTCA others(6235): Show |
chr6 | 44382706 | 44455425 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0016g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0017g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0018g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0020g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0023g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0025g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0026g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0030g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0034g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0001t0035g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0011g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0011g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0011g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0015g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0015g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0027g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0002t0029g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0003t0010g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0019g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0004t0028g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0005t0031g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0006t0012g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0007t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0007t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0008t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0009t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0010t0033g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0011t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0012t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0013t0032g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0001c0014t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| a0002c0015t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | GBR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0156 | EUR | FIN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00323 | hp1 | a0001 | c0001 | t0035 | g0123 | EUR | FIN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00323 | hp2 | a0001 | c0003 | t0003 | g0197 | EUR | FIN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00423 | hp2 | a0001 | c0001 | t0030 | g0098 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00438 | hp1 | a0001 | c0002 | t0015 | g0327 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00544 | hp2 | a0001 | c0002 | t0015 | g0283 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00558 | hp2 | a0001 | c0003 | t0003 | g0172 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00597 | hp2 | a0001 | c0004 | t0004 | g0017 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00639 | hp1 | a0001 | c0003 | t0003 | g0204 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00673 | hp2 | a0001 | c0004 | t0019 | g0193 | EAS | CHS | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00741 | hp1 | a0001 | c0005 | t0002 | g0231 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0171 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0202 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0192 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0325 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0232 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01255 | hp2 | a0001 | c0001 | t0016 | g0137 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01256 | hp2 | a0001 | c0001 | t0034 | g0124 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0211 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0186 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01884 | hp1 | a0001 | c0001 | t0024 | g0027 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01884 | hp2 | a0001 | c0003 | t0010 | g0161 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01891 | hp1 | a0001 | c0004 | t0007 | g0229 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0167 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0203 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01975 | hp1 | a0001 | c0001 | t0020 | g0117 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01975 | hp2 | a0001 | c0002 | t0011 | g0310 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0207 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0188 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01993 | hp2 | a0001 | c0001 | t0008 | g0081 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0293 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02004 | hp2 | a0001 | c0001 | t0014 | g0125 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02083 | hp2 | a0001 | c0002 | t0027 | g0324 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0322 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02145 | hp1 | a0001 | c0004 | t0028 | g0225 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0173 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0210 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0212 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0190 | AMR | PEL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02451 | hp2 | a0001 | c0006 | t0012 | g0002 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | KHV | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02622 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02630 | hp1 | a0001 | c0013 | t0032 | g0146 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0199 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02647 | hp2 | a0001 | c0010 | t0033 | g0153 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0265 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02717 | hp1 | a0001 | c0005 | t0031 | g0257 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02717 | hp2 | a0001 | c0004 | t0007 | g0227 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02723 | hp2 | a0001 | c0005 | t0002 | g0256 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0290 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02886 | hp1 | a0001 | c0004 | t0007 | g0238 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02896 | hp1 | a0001 | c0005 | t0002 | g0236 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02896 | hp2 | a0001 | c0001 | t0023 | g0336 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02897 | hp1 | a0001 | c0005 | t0002 | g0255 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02922 | hp1 | a0001 | c0004 | t0007 | g0241 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02965 | hp1 | a0002 | c0015 | t0013 | g0142 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02965 | hp2 | a0001 | c0004 | t0007 | g0226 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02976 | hp2 | a0001 | c0003 | t0010 | g0338 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03041 | hp1 | a0001 | c0005 | t0002 | g0258 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0084 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03139 | hp2 | a0001 | c0003 | t0010 | g0337 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03195 | hp1 | a0001 | c0004 | t0009 | g0242 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03195 | hp2 | a0001 | c0004 | t0007 | g0239 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03209 | hp1 | a0001 | c0004 | t0009 | g0250 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03239 | hp1 | a0001 | c0004 | t0019 | g0160 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03486 | hp1 | a0001 | c0004 | t0009 | g0252 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0237 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0254 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03492 | hp2 | a0001 | c0001 | t0025 | g0072 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03540 | hp2 | a0001 | c0009 | t0001 | g0145 | AFR | GWD | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0168 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0268 | SAS | BEB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0318 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0200 | SAS | BEB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0157 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0267 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04204 | hp1 | a0001 | c0002 | t0005 | g0234 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0291 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0253 | SAS | STU | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | CHB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | CHB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | CHB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18906 | hp2 | a0001 | c0006 | t0012 | g0002 | AFR | YRI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18945 | hp1 | a0001 | c0004 | t0004 | g0010 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0312 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18948 | hp2 | a0001 | c0003 | t0003 | g0159 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18949 | hp2 | a0001 | c0001 | t0014 | g0106 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18952 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18953 | hp2 | a0001 | c0002 | t0011 | g0321 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18959 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0169 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18962 | hp1 | a0001 | c0014 | t0001 | g0007 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18962 | hp2 | a0001 | c0004 | t0009 | g0248 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0213 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18964 | hp2 | a0001 | c0004 | t0004 | g0182 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18970 | hp1 | a0001 | c0004 | t0004 | g0245 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18972 | hp2 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18973 | hp2 | a0001 | c0004 | t0004 | g0247 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18975 | hp2 | a0001 | c0001 | t0026 | g0219 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18978 | hp1 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0205 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18984 | hp1 | a0001 | c0004 | t0004 | g0220 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18985 | hp1 | a0001 | c0004 | t0004 | g0243 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18985 | hp2 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18993 | hp2 | a0001 | c0004 | t0004 | g0184 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19000 | hp1 | a0001 | c0012 | t0002 | g0301 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19001 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19003 | hp1 | a0001 | c0004 | t0004 | g0246 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19003 | hp2 | a0001 | c0001 | t0018 | g0108 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0209 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0133 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19043 | hp1 | a0001 | c0004 | t0007 | g0240 | AFR | LWK | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19062 | hp2 | a0001 | c0004 | t0004 | g0244 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19066 | hp1 | a0001 | c0003 | t0003 | g0191 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19072 | hp1 | a0001 | c0007 | t0002 | g0147 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19075 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19080 | hp1 | a0001 | c0007 | t0002 | g0040 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19085 | hp1 | a0001 | c0002 | t0004 | g0309 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19086 | hp2 | a0001 | c0002 | t0029 | g0333 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19087 | hp2 | a0001 | c0004 | t0004 | g0183 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19088 | hp1 | a0001 | c0004 | t0004 | g0010 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19089 | hp1 | a0001 | c0004 | t0004 | g0181 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19089 | hp2 | a0001 | c0002 | t0011 | g0280 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19090 | hp1 | a0001 | c0011 | t0002 | g0166 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19091 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20129 | hp1 | a0001 | c0002 | t0021 | g0311 | AFR | ASW | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20129 | hp2 | a0001 | c0006 | t0012 | g0002 | AFR | ASW | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0270 | EUR | TSI | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0319 | SAS | GIH | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0174 | AMR | CLM | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02486 | hp1 | a0001 | c0004 | t0007 | g0228 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG02559 | hp2 | a0001 | c0008 | t0022 | g0144 | AFR | ACB | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| HG06807 | hp2 | a0001 | c0004 | t0009 | g0249 | AFR | USA | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| NA21309 | hp2 | a0001 | c0004 | t0009 | g0251 | AFR | LWK | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0195 | REF | REF | CDC5L_chr6_44382706_44455425 | CDC5L | chr6 | 44382706 | 44455425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44422781 | A | G | 1 | a0002 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1376A>G | p.Tyr459Cys | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/16 | 1494/6241 | 1376/2409 | 459/802 | chr6 | 44422781 | |||
| chr6:44445723 | G | C | 1 | a0002 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2160G>C | p.Leu720Phe | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/16 | 2278/6241 | 2160/2409 | 720/802 | chr6 | 44445723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44390270 | T | C | 2 | a0001c0008 a0001c0009 |
2 | HG02559.hp2 HG03540.hp2 |
splice_region_variant&synonymous_variant | LOW | c.48T>C | p.Asp16Asp | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/16 | 166/6241 | 48/2409 | 16/802 | chr6 | 44390270 | |||
| chr6:44390288 | G | A | 1 | a0001c0010 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.66G>A | p.Ala22Ala | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/16 | 184/6241 | 66/2409 | 22/802 | chr6 | 44390288 | |||
| chr6:44392796 | G | A | 3 | a0001c0003 a0001c0011 a0001c0012 |
45 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
synonymous_variant | LOW | c.279G>A | p.Ala93Ala | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/16 | 397/6241 | 279/2409 | 93/802 | chr6 | 44392796 | |||
| chr6:44403953 | T | C | 3 | a0001c0006 a0001c0010 a0001c0013 |
5 | HG02451.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.684T>C | p.Ser228Ser | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/16 | 802/6241 | 684/2409 | 228/802 | chr6 | 44403953 | |||
| chr6:44403977 | C | T | 5 | a0001c0002 a0001c0004 a0001c0005 others(2): Show |
132 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(129): Show |
synonymous_variant | LOW | c.708C>T | p.Asp236Asp | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/16 | 826/6241 | 708/2409 | 236/802 | chr6 | 44403977 | |||
| chr6:44408455 | A | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.915A>G | p.Ala305Ala | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/16 | 1033/6241 | 915/2409 | 305/802 | chr6 | 44408455 | |||
| chr6:44419568 | T | C | 1 | a0001c0005 | 8 | HG00741.hp1 HG01243.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.1212T>C | p.Thr404Thr | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/16 | 1330/6241 | 1212/2409 | 404/802 | chr6 | 44419568 | |||
| chr6:44422716 | T | C | 1 | a0001c0014 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.1311T>C | p.Ser437Ser | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/16 | 1429/6241 | 1311/2409 | 437/802 | chr6 | 44422716 | |||
| chr6:44426685 | T | C | 1 | a0001c0006 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1854T>C | p.His618His | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/16 | 1972/6241 | 1854/2409 | 618/802 | chr6 | 44426685 | |||
| chr6:44445726 | T | A | 4 | a0001c0002 a0001c0005 a0001c0007 others(1): Show |
103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
synonymous_variant | LOW | c.2163T>A | p.Leu721Leu | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/16 | 2281/6241 | 2163/2409 | 721/802 | chr6 | 44445726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44446722 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG00323.hp1 HG01256.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 11 | chr6 | 44446722 | ||||||
| chr6:44447015 | T | G | 1 | a0001c0001t0020 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 304 | chr6 | 44447015 | ||||||
| chr6:44447266 | AT | A | 3 | a0001c0001t0003 a0001c0002t0021 a0001c0003t0003 |
44 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*565delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 565 | INFO_REALIGN_3_PRIME | chr6 | 44447266 | |||||
| chr6:44447364 | C | G | 1 | a0001c0004t0019 | 2 | HG00673.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 653 | chr6 | 44447364 | ||||||
| chr6:44447507 | T | C | 1 | a0001c0008t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 796 | chr6 | 44447507 | ||||||
| chr6:44448048 | C | G | 2 | a0001c0010t0033 a0001c0013t0032 |
2 | HG02630.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1337C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1337 | chr6 | 44448048 | ||||||
| chr6:44448066 | C | T | 1 | a0001c0005t0031 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1355C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1355 | chr6 | 44448066 | ||||||
| chr6:44448118 | CAT | C | 11 | a0001c0001t0003 a0001c0001t0030 a0001c0002t0004 others(8): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1408_*1409delAT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1408 | chr6 | 44448118 | ||||||
| chr6:44448340 | A | G | 1 | a0001c0006t0012 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1629A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1629 | chr6 | 44448340 | ||||||
| chr6:44448382 | C | T | 1 | a0001c0001t0018 | 2 | NA18952.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1671 | chr6 | 44448382 | ||||||
| chr6:44448637 | AAGTT | A | 6 | a0001c0001t0003 a0001c0001t0030 a0001c0002t0004 others(3): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1930delAGTT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 1927 | chr6 | 44448637 | ||||||
| chr6:44448899 | G | T | 1 | a0001c0001t0017 | 2 | HG01891.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2188 | chr6 | 44448899 | ||||||
| chr6:44448915 | C | T | 1 | a0001c0002t0027 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2204C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2204 | chr6 | 44448915 | ||||||
| chr6:44449081 | C | T | 2 | a0001c0001t0017 a0001c0006t0012 |
5 | HG01891.hp2 HG02451.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2370C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2370 | chr6 | 44449081 | ||||||
| chr6:44449181 | TAAA | T | 21 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0016 others(18): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*2475_*2477delAAA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2475 | INFO_REALIGN_3_PRIME | chr6 | 44449181 | |||||
| chr6:44449302 | T | G | 1 | a0001c0003t0010 | 3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2591T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2591 | chr6 | 44449302 | ||||||
| chr6:44449513 | A | T | 1 | a0001c0001t0025 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2802A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2802 | chr6 | 44449513 | ||||||
| chr6:44449601 | C | T | 1 | a0001c0010t0033 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2890C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2890 | chr6 | 44449601 | ||||||
| chr6:44449700 | A | G | 1 | a0001c0001t0024 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2989A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2989 | chr6 | 44449700 | ||||||
| chr6:44449705 | A | T | 6 | a0001c0001t0003 a0001c0001t0030 a0001c0002t0004 others(3): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2994A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 2994 | chr6 | 44449705 | ||||||
| chr6:44449748 | T | C | 1 | a0001c0004t0028 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3037T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3037 | chr6 | 44449748 | ||||||
| chr6:44449864 | C | CT | 5 | a0001c0001t0014 a0001c0001t0026 a0001c0001t0030 others(2): Show |
8 | HG00423.hp2 HG01884.hp2 HG02004.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3171dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3172 | INFO_REALIGN_3_PRIME | chr6 | 44449864 | |||||
| chr6:44449864 | C | CTT | 3 | a0001c0001t0016 a0001c0004t0007 a0001c0004t0028 |
11 | HG01255.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3170_*3171dupTT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3172 | INFO_REALIGN_3_PRIME | chr6 | 44449864 | |||||
| chr6:44449864 | CT | C | 5 | a0001c0001t0013 a0001c0001t0034 a0001c0002t0011 others(2): Show |
7 | HG01256.hp2 HG01975.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3171delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3171 | INFO_REALIGN_3_PRIME | chr6 | 44449864 | |||||
| chr6:44449924 | G | A | 3 | a0001c0001t0016 a0001c0004t0007 a0001c0004t0028 |
11 | HG01255.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3213G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3213 | chr6 | 44449924 | ||||||
| chr6:44449993 | A | G | 1 | a0001c0001t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3282A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3282 | chr6 | 44449993 | ||||||
| chr6:44450021 | AC | A | 19 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0030 others(16): Show |
167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3312delC | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr6 | 44450021 | |||||
| chr6:44450053 | G | A | 1 | a0001c0002t0015 | 2 | HG00438.hp1 HG00544.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3342G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3342 | chr6 | 44450053 | ||||||
| chr6:44450060 | T | C | 6 | a0001c0001t0005 a0001c0001t0017 a0001c0002t0005 others(3): Show |
20 | HG00673.hp2 HG01891.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3349T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3349 | chr6 | 44450060 | ||||||
| chr6:44450141 | GGT | G | 1 | a0001c0001t0008 | 6 | HG00408.hp1 HG01993.hp2 NA18990.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3434_*3435delTG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3434 | INFO_REALIGN_3_PRIME | chr6 | 44450141 | |||||
| chr6:44450183 | T | C | 3 | a0001c0001t0005 a0001c0002t0005 a0001c0004t0019 |
14 | HG00673.hp2 HG02572.hp2 HG02723.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3472T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3472 | chr6 | 44450183 | ||||||
| chr6:44450329 | A | G | 9 | a0001c0002t0002 a0001c0002t0011 a0001c0002t0015 others(6): Show |
95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*3618A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 16/16 | 3618 | chr6 | 44450329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44387897 | C | T | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45+29C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387897 | |||||||
| chr6:44387898 | C | T | 1 | a0001c0001t0023g0336 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+30C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387898 | |||||||
| chr6:44387927 | C | G | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45+59C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387927 | |||||||
| chr6:44387940 | C | CG | 35 | a0001c0002t0002g0230 a0001c0002t0005g0233 a0001c0002t0005g0234 others(32): Show |
36 | HG00597.hp1 HG00741.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.45+79dupG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44387940 | ||||||
| chr6:44387940 | C | CGG | 79 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0259 others(76): Show |
81 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.45+78_45+79dupGG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44387940 | ||||||
| chr6:44387945 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.45+77G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387945 | |||||||
| chr6:44387946 | G | GT | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+78_45+79insT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387946 | |||||||
| chr6:44387962 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.45+94T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387962 | |||||||
| chr6:44387989 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+121G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44387989 | |||||||
| chr6:44388021 | T | C | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.45+153T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388021 | |||||||
| chr6:44388144 | A | ACCCCCGC others(4): Show |
1 | a0001c0004t0028g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+280_45+281insCG others(9): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388144 | ||||||
| chr6:44388144 | A | ACCCCGCC others(1): Show |
18 | a0001c0001t0017g0199 a0001c0003t0003g0009 a0001c0003t0003g0200 others(15): Show |
19 | HG00639.hp1 HG01081.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.45+289_45+296dupGC others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388144 | ||||||
| chr6:44388144 | A | ACCCCGCC others(2): Show |
8 | a0001c0001t0017g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(5): Show |
8 | HG00544.hp1 HG00558.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+280_45+288dupCG others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388144 | ||||||
| chr6:44388146 | C | T | 1 | a0001c0002t0002g0335 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.45+278C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388146 | |||||||
| chr6:44388149 | G | C | 1 | a0001c0004t0028g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+281G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388149 | |||||||
| chr6:44388149 | G | GC | 36 | a0001c0001t0001g0039 a0001c0001t0001g0162 a0001c0001t0001g0163 others(33): Show |
37 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+288dupC | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388149 | G | GCCCCCCC others(3): Show |
2 | a0001c0004t0007g0228 a0001c0004t0007g0229 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.45+288_45+289insCC others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388149 | G | GCCCCCCC others(4): Show |
1 | a0001c0004t0007g0227 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+288_45+289insCC others(9): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388149 | G | GCCCCCCC others(5): Show |
1 | a0001c0004t0007g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.45+288_45+289insCC others(10): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388149 | G | GCCCCCCC others(3): Show |
4 | a0001c0003t0003g0156 a0001c0003t0003g0157 a0001c0003t0003g0158 others(1): Show |
4 | HG00280.hp2 HG04199.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+288_45+289insCG others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388149 | G | GCCCCCCC others(2): Show |
9 | a0001c0003t0003g0185 a0001c0003t0003g0186 a0001c0003t0003g0187 others(6): Show |
9 | HG01109.hp1 HG01361.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+290_45+298dupCC others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388149 | ||||||
| chr6:44388155 | C | CCCCG | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+288_45+289insCC others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388155 | ||||||
| chr6:44388155 | C | CCCG | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(48): Show |
53 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.45+288_45+289insCG others(1): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388155 | ||||||
| chr6:44388156 | C | CCG | 14 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
15 | HG01884.hp1 HG02015.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+288_45+289insCG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388156 | |||||||
| chr6:44388156 | C | CCGCCCCC others(3): Show |
2 | a0001c0003t0003g0165 a0001c0011t0002g0166 |
2 | NA19075.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.45+288_45+289insCG others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388156 | |||||||
| chr6:44388156 | CG | C | 45 | a0001c0001t0005g0154 a0001c0002t0002g0011 a0001c0002t0002g0148 others(42): Show |
46 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.45+289delG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388156 | |||||||
| chr6:44388157 | G | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
165 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.45+289G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388157 | |||||||
| chr6:44388157 | G | GC | 34 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0091 others(31): Show |
35 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.45+297dupC | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388157 | ||||||
| chr6:44388157 | G | GCC | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+296_45+297dupCC | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388157 | ||||||
| chr6:44388157 | G | GCCCCCCC others(3): Show |
1 | a0001c0003t0003g0198 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.45+298_45+299insCC others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388157 | ||||||
| chr6:44388161 | C | T | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+293C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388161 | |||||||
| chr6:44388162 | C | T | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+294C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388162 | |||||||
| chr6:44388165 | C | T | 16 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.45+297C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388165 | |||||||
| chr6:44388176 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+308A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388176 | |||||||
| chr6:44388367 | ATC | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+505_45+506delCT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388367 | ||||||
| chr6:44388492 | GTC | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+628_45+629delCT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388492 | ||||||
| chr6:44388555 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.45+687G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388555 | |||||||
| chr6:44388563 | GA | G | 100 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(97): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+698delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388563 | ||||||
| chr6:44388675 | C | CT | 39 | a0001c0001t0001g0088 a0001c0001t0001g0163 a0001c0001t0001g0217 others(36): Show |
41 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+824dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388675 | ||||||
| chr6:44388675 | C | CTT | 32 | a0001c0003t0003g0009 a0001c0003t0003g0158 a0001c0003t0003g0159 others(29): Show |
33 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.45+823_45+824dupTT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388675 | ||||||
| chr6:44388675 | CT | C | 21 | a0001c0001t0001g0090 a0001c0002t0002g0259 a0001c0004t0004g0010 others(18): Show |
22 | HG00673.hp2 HG01891.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+824delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388675 | ||||||
| chr6:44388760 | C | A | 5 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(2): Show |
5 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+892C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388760 | |||||||
| chr6:44388875 | C | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+1007C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44388875 | |||||||
| chr6:44388940 | TA | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.45+1074delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 44388940 | ||||||
| chr6:44389039 | C | T | 7 | a0001c0004t0004g0010 a0001c0004t0004g0243 a0001c0004t0004g0244 others(4): Show |
8 | NA18945.hp1 NA18962.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+1171C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389039 | |||||||
| chr6:44389456 | G | A | 6 | a0001c0002t0002g0259 a0001c0002t0002g0260 a0001c0002t0002g0261 others(3): Show |
6 | HG00423.hp1 HG00438.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-812G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389456 | |||||||
| chr6:44389461 | A | G | 14 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 others(11): Show |
14 | HG00621.hp2 HG02015.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-807A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389461 | |||||||
| chr6:44389496 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46-772A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389496 | |||||||
| chr6:44389576 | T | C | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-692T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389576 | |||||||
| chr6:44389650 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.46-618G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389650 | |||||||
| chr6:44389734 | G | A | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.46-534G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389734 | |||||||
| chr6:44389923 | T | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-345T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389923 | |||||||
| chr6:44389925 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.46-343C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389925 | |||||||
| chr6:44389948 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-320C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44389948 | |||||||
| chr6:44390104 | A | C | 1 | a0001c0001t0005g0196 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46-164A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390104 | |||||||
| chr6:44390127 | C | CTTGTTCT others(18): Show |
1 | a0001c0001t0005g0196 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46-141_46-140insTT others(23): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390127 | |||||||
| chr6:44390127 | C | T | 1 | a0001c0002t0002g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.46-141C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390127 | |||||||
| chr6:44390129 | T | C | 1 | a0001c0001t0005g0196 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46-139T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390129 | |||||||
| chr6:44390147 | T | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.46-121T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390147 | |||||||
| chr6:44390169 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-99T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390169 | |||||||
| chr6:44390171 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-97T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390171 | |||||||
| chr6:44390181 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-87C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390181 | |||||||
| chr6:44390182 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-86A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390182 | |||||||
| chr6:44390183 | A | G | 1 | a0001c0002t0002g0334 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46-85A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390183 | |||||||
| chr6:44390184 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-84T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390184 | |||||||
| chr6:44390185 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-83A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390185 | |||||||
| chr6:44390187 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-81C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390187 | |||||||
| chr6:44390192 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.46-76T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390192 | |||||||
| chr6:44390201 | A | G | 1 | a0002c0015t0013g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46-67A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390201 | |||||||
| chr6:44390238 | C | G | 1 | a0001c0004t0028g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.46-30C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 1/15 | chr6 | 44390238 | |||||||
| chr6:44390707 | T | G | 102 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(99): Show |
104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.149+336T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44390707 | |||||||
| chr6:44390711 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.149+340C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44390711 | |||||||
| chr6:44390746 | A | G | 1 | a0001c0002t0002g0290 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.149+375A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44390746 | |||||||
| chr6:44390882 | ATATAT | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.149+517_149+521del others(5): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390882 | ||||||
| chr6:44390906 | A | AATGTTAT others(25): Show |
1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.149+689_149+720dup others(32): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390906 | ||||||
| chr6:44390906 | AATGTTAT others(25): Show |
A | 35 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
35 | HG00621.hp2 HG01069.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.149+689_149+720del others(32): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390906 | ||||||
| chr6:44390906 | AATGTTAT others(57): Show |
A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.149+657_149+720del others(64): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390906 | ||||||
| chr6:44390916 | A | ATTATATA others(18): Show |
4 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(1): Show |
4 | HG03195.hp1 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+556_149+580dup others(25): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390916 | ||||||
| chr6:44390929 | CATATTTA others(27): Show |
C | 2 | a0001c0001t0001g0044 a0001c0003t0010g0161 |
2 | HG01884.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.149+561_149+594del others(34): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390929 | ||||||
| chr6:44390931 | T | TATTTAAT others(23): Show |
1 | a0001c0005t0031g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.149+563_149+592dup others(30): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390931 | ||||||
| chr6:44390934 | T | TTAATATG others(21): Show |
1 | a0001c0002t0002g0296 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.149+566_149+593dup others(28): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390934 | ||||||
| chr6:44390941 | GTTATATA others(64): Show |
G | 2 | a0001c0001t0001g0099 a0001c0001t0024g0027 |
2 | HG01884.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.149+581_149+651del others(71): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390941 | ||||||
| chr6:44390955 | ATTAAACA others(59): Show |
A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0097 |
3 | HG02735.hp1 HG02818.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.149+585_149+650del others(66): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44390955 | |||||||
| chr6:44390973 | GTTATATA others(64): Show |
G | 1 | a0001c0001t0001g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.149+613_149+683del others(71): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390973 | ||||||
| chr6:44390993 | CAT | C | 3 | a0001c0003t0010g0161 a0001c0008t0022g0144 a0001c0009t0001g0145 |
3 | HG01884.hp2 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.149+625_149+626del others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44390993 | ||||||
| chr6:44391025 | CAT | C | 3 | a0001c0001t0030g0098 a0001c0002t0002g0270 a0001c0002t0002g0299 |
3 | HG00423.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.149+657_149+658del others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391025 | ||||||
| chr6:44391025 | CATATTTA others(89): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.149+657_149+752del others(96): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391025 | ||||||
| chr6:44391027 | TATTTAAT others(55): Show |
T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0100 others(1): Show |
4 | HG00733.hp2 HG01123.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+721_149+782del others(62): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391027 | ||||||
| chr6:44391037 | GTTATATA others(32): Show |
G | 7 | a0001c0002t0002g0230 a0001c0002t0002g0281 a0001c0002t0002g0282 others(4): Show |
7 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+677_149+715del others(39): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391037 | ||||||
| chr6:44391044 | A | ATTAAACA others(16): Show |
2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.149+676_149+677ins others(23): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391044 | ||||||
| chr6:44391059 | TATTTAAT others(23): Show |
T | 2 | a0001c0001t0030g0098 a0001c0006t0012g0002 |
4 | HG00423.hp2 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+721_149+750del others(30): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391059 | ||||||
| chr6:44391062 | TTAATATG others(50): Show |
T | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.149+692_149+748del others(57): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391062 | |||||||
| chr6:44391069 | GTTATATA | G | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+709_149+715del others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391069 | ||||||
| chr6:44391076 | A | ATTATATA others(18): Show |
12 | a0001c0002t0002g0267 a0001c0002t0002g0296 a0001c0004t0007g0226 others(9): Show |
12 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.149+720_149+721ins others(25): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(50): Show |
81 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(78): Show |
82 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.149+720_149+721ins others(57): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(75): Show |
1 | a0001c0002t0002g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.149+720_149+721ins others(82): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(82): Show |
3 | a0001c0002t0002g0297 a0001c0002t0002g0318 a0001c0002t0002g0334 |
3 | HG04115.hp1 NA19063.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.149+720_149+721ins others(89): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(114): Show |
2 | a0001c0002t0002g0265 a0001c0005t0002g0256 |
2 | HG02683.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.149+720_149+721ins others(121): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(178): Show |
1 | a0001c0002t0027g0324 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.149+720_149+721ins others(185): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTATATA others(52): Show |
2 | a0001c0002t0002g0270 a0001c0002t0002g0299 |
2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.149+720_149+721ins others(59): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | ATTCTATA others(50): Show |
1 | a0001c0002t0002g0278 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.149+707_149+708ins others(57): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391076 | ||||||
| chr6:44391076 | A | G | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.149+705A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391076 | |||||||
| chr6:44391089 | C | CAT | 4 | a0001c0002t0002g0263 a0001c0003t0003g0202 a0001c0004t0019g0160 others(1): Show |
4 | HG00673.hp2 HG01081.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+719_149+720dup others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391089 | ||||||
| chr6:44391096 | T | TATGTTAT others(23): Show |
46 | a0001c0003t0003g0009 a0001c0003t0003g0156 a0001c0003t0003g0157 others(43): Show |
48 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.149+728_149+757dup others(30): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391096 | ||||||
| chr6:44391096 | T | TATGTTAT others(53): Show |
1 | a0001c0003t0003g0202 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+750_149+751ins others(60): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391096 | ||||||
| chr6:44391121 | T | TATTTAAT others(16): Show |
1 | a0001c0002t0002g0263 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.149+770_149+771ins others(23): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391121 | ||||||
| chr6:44391131 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.149+760G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391131 | |||||||
| chr6:44391151 | CAT | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.149+783_149+784del others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391151 | ||||||
| chr6:44391171 | TTG | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.149+802_149+803del others(2): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44391171 | ||||||
| chr6:44391182 | A | G | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.149+811A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391182 | |||||||
| chr6:44391213 | G | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.149+842G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391213 | |||||||
| chr6:44391232 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.149+861C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391232 | |||||||
| chr6:44391271 | C | T | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.149+900C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391271 | |||||||
| chr6:44391349 | C | T | 2 | a0001c0006t0012g0002 a0002c0015t0013g0142 |
4 | HG02451.hp2 HG02965.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+978C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391349 | |||||||
| chr6:44391438 | C | T | 15 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0002g0286 others(12): Show |
15 | HG00558.hp1 HG00673.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+1067C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391438 | |||||||
| chr6:44391493 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0103 others(1): Show |
4 | HG03209.hp2 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1122C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391493 | |||||||
| chr6:44391537 | C | T | 135 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0217 others(132): Show |
137 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.150-1130C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391537 | |||||||
| chr6:44391613 | T | A | 1 | a0001c0002t0002g0332 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.150-1054T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44391613 | |||||||
| chr6:44392000 | CTGT | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.150-665_150-663del others(3): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 44392000 | ||||||
| chr6:44392007 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0014g0106 |
2 | NA18949.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.150-660G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392007 | |||||||
| chr6:44392050 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.150-617T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392050 | |||||||
| chr6:44392076 | T | C | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.150-591T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392076 | |||||||
| chr6:44392104 | T | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.150-563T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392104 | |||||||
| chr6:44392137 | A | T | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.150-530A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392137 | |||||||
| chr6:44392147 | T | A | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-520T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392147 | |||||||
| chr6:44392277 | T | G | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.150-390T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392277 | |||||||
| chr6:44392418 | T | A | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.150-249T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392418 | |||||||
| chr6:44392430 | T | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-237T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 2/15 | chr6 | 44392430 | |||||||
| chr6:44392943 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.311+115A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | chr6 | 44392943 | |||||||
| chr6:44392952 | C | G | 7 | a0001c0002t0002g0230 a0001c0002t0002g0281 a0001c0002t0002g0282 others(4): Show |
7 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+124C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | chr6 | 44392952 | |||||||
| chr6:44393077 | GA | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | NA18747.hp1 NA18994.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+255delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 44393077 | ||||||
| chr6:44393134 | C | G | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.311+306C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | chr6 | 44393134 | |||||||
| chr6:44393164 | G | GT | 62 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0048 others(59): Show |
64 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.312-257dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 44393164 | ||||||
| chr6:44393164 | GT | G | 19 | a0001c0001t0001g0032 a0001c0001t0001g0050 a0001c0001t0001g0096 others(16): Show |
19 | HG01169.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.312-257delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 44393164 | ||||||
| chr6:44393189 | T | A | 16 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(13): Show |
16 | HG00673.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.312-257T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 3/15 | chr6 | 44393189 | |||||||
| chr6:44393714 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+141G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44393714 | |||||||
| chr6:44393786 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+213T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44393786 | |||||||
| chr6:44393905 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+332A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44393905 | |||||||
| chr6:44394017 | A | G | 1 | a0001c0003t0003g0185 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.439+444A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394017 | |||||||
| chr6:44394124 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+551A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394124 | |||||||
| chr6:44394522 | T | A | 1 | a0001c0004t0019g0193 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.439+949T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394522 | |||||||
| chr6:44394611 | G | A | 1 | a0001c0001t0006g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.439+1038G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394611 | |||||||
| chr6:44394627 | G | A | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.439+1054G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394627 | |||||||
| chr6:44394656 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18970.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.439+1083G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394656 | |||||||
| chr6:44394692 | T | TA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0051 others(4): Show |
7 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+1126dupA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394692 | ||||||
| chr6:44394713 | CAGGTGTG others(32): Show |
C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.439+1144_439+1182d others(41): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394713 | ||||||
| chr6:44394793 | T | C | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.439+1220T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394793 | |||||||
| chr6:44394855 | CA | C | 40 | a0001c0001t0006g0176 a0001c0003t0003g0009 a0001c0003t0003g0156 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.439+1312delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAA | C | 26 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(23): Show |
26 | HG00621.hp2 HG00673.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.439+1311_439+1312d others(4): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAA | C | 26 | a0001c0001t0006g0221 a0001c0002t0002g0148 a0001c0002t0002g0152 others(23): Show |
26 | HG00741.hp1 HG01243.hp1 HG02630.hp1 others(23): Show |
intron_variant | MODIFIER | c.439+1310_439+1312d others(5): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAAA | C | 78 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0149 others(75): Show |
80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.439+1309_439+1312d others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAAAA | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0048 others(16): Show |
19 | HG00423.hp2 HG00673.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+1308_439+1312d others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAAAAA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.439+1307_439+1312d others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAAAAAA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0041 others(14): Show |
17 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.439+1306_439+1312d others(9): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394855 | CAAAAAAA others(7): Show |
C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+1299_439+1312d others(16): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394855 | ||||||
| chr6:44394881 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+1308A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394881 | |||||||
| chr6:44394889 | TATAC | T | 12 | a0001c0004t0004g0010 a0001c0004t0004g0243 a0001c0004t0004g0244 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.439+1318_439+1321d others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394889 | ||||||
| chr6:44394889 | TATACAC | T | 109 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(106): Show |
111 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.439+1318_439+1323d others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394889 | ||||||
| chr6:44394891 | T | TACAC | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.439+1343_439+1346d others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394891 | ||||||
| chr6:44394891 | TACAC | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0051 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+1343_439+1346d others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394891 | ||||||
| chr6:44394891 | TACACAC | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.439+1341_439+1346d others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 44394891 | ||||||
| chr6:44394950 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0110 |
2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.439+1377A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44394950 | |||||||
| chr6:44395256 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.440-1085G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395256 | |||||||
| chr6:44395429 | A | G | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-912A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395429 | |||||||
| chr6:44395493 | A | T | 41 | a0001c0003t0003g0009 a0001c0003t0003g0156 a0001c0003t0003g0157 others(38): Show |
42 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.440-848A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395493 | |||||||
| chr6:44395637 | G | C | 1 | a0001c0002t0002g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.440-704G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395637 | |||||||
| chr6:44395725 | G | A | 1 | a0001c0001t0006g0177 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.440-616G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395725 | |||||||
| chr6:44395768 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.440-573T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395768 | |||||||
| chr6:44395835 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.440-506A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395835 | |||||||
| chr6:44395969 | A | G | 1 | a0001c0004t0009g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.440-372A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44395969 | |||||||
| chr6:44396133 | G | C | 2 | a0001c0003t0003g0168 a0001c0003t0003g0200 |
2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.440-208G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44396133 | |||||||
| chr6:44396274 | A | G | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440-67A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44396274 | |||||||
| chr6:44396277 | C | T | 1 | a0001c0002t0027g0324 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.440-64C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 4/15 | chr6 | 44396277 | |||||||
| chr6:44396481 | C | T | 1 | a0001c0002t0002g0262 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.539+41C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44396481 | |||||||
| chr6:44396489 | A | T | 1 | a0001c0002t0002g0262 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.539+49A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44396489 | |||||||
| chr6:44396524 | G | GT | 24 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0041 others(21): Show |
24 | HG01109.hp1 HG01123.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.539+99dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 44396524 | ||||||
| chr6:44396524 | GT | G | 15 | a0001c0001t0001g0217 a0001c0001t0006g0176 a0001c0001t0006g0177 others(12): Show |
15 | HG01255.hp1 HG02015.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.539+99delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 44396524 | ||||||
| chr6:44396867 | G | A | 1 | a0001c0002t0002g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.539+427G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44396867 | |||||||
| chr6:44397079 | A | G | 1 | a0001c0004t0019g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.539+639A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397079 | |||||||
| chr6:44397098 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.539+658C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397098 | |||||||
| chr6:44397167 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.539+727T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397167 | |||||||
| chr6:44397202 | A | C | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.539+762A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397202 | |||||||
| chr6:44397264 | C | T | 1 | a0001c0003t0003g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.539+824C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397264 | |||||||
| chr6:44397298 | T | A | 1 | a0001c0003t0003g0207 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.539+858T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397298 | |||||||
| chr6:44397298 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
16 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.539+858T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397298 | |||||||
| chr6:44397413 | C | T | 2 | a0001c0003t0003g0156 a0001c0003t0003g0157 |
2 | HG00280.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.539+973C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397413 | |||||||
| chr6:44397440 | C | A | 1 | a0001c0002t0002g0282 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.539+1000C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397440 | |||||||
| chr6:44397498 | A | G | 5 | a0001c0002t0002g0259 a0001c0002t0002g0260 a0001c0002t0002g0261 others(2): Show |
5 | HG00423.hp1 NA18982.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1058A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397498 | |||||||
| chr6:44397518 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.539+1078C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397518 | |||||||
| chr6:44397648 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.539+1208T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397648 | |||||||
| chr6:44397919 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.539+1479A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44397919 | |||||||
| chr6:44398114 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.539+1674A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398114 | |||||||
| chr6:44398149 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.539+1709G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398149 | |||||||
| chr6:44398325 | C | T | 51 | a0001c0003t0003g0009 a0001c0003t0003g0156 a0001c0003t0003g0157 others(48): Show |
53 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+1885C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398325 | |||||||
| chr6:44398605 | T | C | 1 | a0001c0005t0002g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.539+2165T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398605 | |||||||
| chr6:44398691 | G | T | 3 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0224 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.539+2251G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398691 | |||||||
| chr6:44398761 | A | C | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.539+2321A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398761 | |||||||
| chr6:44398883 | C | T | 3 | a0001c0002t0002g0329 a0001c0002t0002g0330 a0001c0002t0002g0331 |
3 | HG02135.hp2 NA18941.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.539+2443C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44398883 | |||||||
| chr6:44399256 | C | A | 5 | a0001c0002t0005g0233 a0001c0002t0005g0234 a0001c0002t0005g0237 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+2816C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399256 | |||||||
| chr6:44399442 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.539+3002C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399442 | |||||||
| chr6:44399471 | G | A | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.539+3031G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399471 | |||||||
| chr6:44399774 | C | T | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.539+3334C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399774 | |||||||
| chr6:44399844 | G | A | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.539+3404G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399844 | |||||||
| chr6:44399903 | G | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.539+3463G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44399903 | |||||||
| chr6:44400020 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.539+3580T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44400020 | |||||||
| chr6:44400397 | T | C | 2 | a0001c0002t0002g0284 a0001c0002t0002g0286 |
2 | NA18948.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.540-3412T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44400397 | |||||||
| chr6:44400446 | G | C | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.540-3363G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44400446 | |||||||
| chr6:44400672 | G | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540-3137G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44400672 | |||||||
| chr6:44401043 | A | G | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.540-2766A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401043 | |||||||
| chr6:44401314 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540-2495G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401314 | |||||||
| chr6:44401315 | TCCGC | T | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.540-2489_540-2486d others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 44401315 | ||||||
| chr6:44401468 | C | T | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.540-2341C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401468 | |||||||
| chr6:44401643 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.540-2166T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401643 | |||||||
| chr6:44401649 | T | A | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-2160T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401649 | |||||||
| chr6:44401676 | T | A | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-2133T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401676 | |||||||
| chr6:44401676 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540-2133T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401676 | |||||||
| chr6:44401717 | A | T | 1 | a0001c0001t0005g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.540-2092A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401717 | |||||||
| chr6:44401778 | A | G | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.540-2031A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401778 | |||||||
| chr6:44401875 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.540-1934G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401875 | |||||||
| chr6:44401877 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
5 | HG02040.hp2 NA18956.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1932T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44401877 | |||||||
| chr6:44402074 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.540-1735T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402074 | |||||||
| chr6:44402103 | C | T | 2 | a0001c0002t0002g0269 a0001c0002t0002g0279 |
2 | NA18995.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.540-1706C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402103 | |||||||
| chr6:44402167 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.540-1642C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402167 | |||||||
| chr6:44402335 | A | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1474A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402335 | |||||||
| chr6:44402580 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0082 |
3 | HG02015.hp1 NA18972.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.540-1229A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402580 | |||||||
| chr6:44402624 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1185G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402624 | |||||||
| chr6:44402835 | A | G | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.540-974A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402835 | |||||||
| chr6:44402884 | T | C | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.540-925T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44402884 | |||||||
| chr6:44403330 | TA | T | 41 | a0001c0002t0015g0327 a0001c0003t0003g0009 a0001c0003t0003g0156 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.540-464delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 44403330 | ||||||
| chr6:44403343 | A | C | 127 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(124): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.540-466A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44403343 | |||||||
| chr6:44403449 | A | T | 1 | a0001c0003t0003g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.540-360A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44403449 | |||||||
| chr6:44403556 | G | A | 3 | a0001c0003t0010g0161 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.540-253G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44403556 | |||||||
| chr6:44403663 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-146G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 5/15 | chr6 | 44403663 | |||||||
| chr6:44404092 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+65G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404092 | |||||||
| chr6:44404618 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
5 | HG02040.hp2 NA18956.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.758+591T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404618 | |||||||
| chr6:44404711 | T | G | 40 | a0001c0003t0003g0009 a0001c0003t0003g0156 a0001c0003t0003g0157 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.758+684T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404711 | |||||||
| chr6:44404721 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.758+694G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404721 | |||||||
| chr6:44404733 | T | C | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+706T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404733 | |||||||
| chr6:44404805 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.758+778A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404805 | |||||||
| chr6:44404828 | G | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.758+801G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404828 | |||||||
| chr6:44404879 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.758+852A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404879 | |||||||
| chr6:44404892 | C | T | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+865C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404892 | |||||||
| chr6:44404974 | A | G | 1 | a0001c0002t0002g0264 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.758+947A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404974 | |||||||
| chr6:44404978 | G | A | 1 | a0001c0012t0002g0301 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.758+951G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44404978 | |||||||
| chr6:44405056 | A | C | 1 | a0001c0001t0008g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.758+1029A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405056 | |||||||
| chr6:44405139 | T | C | 1 | a0001c0005t0002g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.758+1112T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405139 | |||||||
| chr6:44405142 | T | G | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.758+1115T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405142 | |||||||
| chr6:44405264 | T | TA | 4 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0136 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-1058dupA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 44405264 | ||||||
| chr6:44405536 | G | A | 11 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(8): Show |
11 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.759-787G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405536 | |||||||
| chr6:44405797 | C | T | 1 | a0001c0002t0002g0328 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.759-526C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405797 | |||||||
| chr6:44405876 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.759-447G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405876 | |||||||
| chr6:44405895 | T | C | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.759-428T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44405895 | |||||||
| chr6:44406123 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.759-200A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 6/15 | chr6 | 44406123 | |||||||
| chr6:44406527 | A | G | 1 | a0001c0001t0005g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.903+60A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406527 | |||||||
| chr6:44406624 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.903+157G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406624 | |||||||
| chr6:44406680 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.903+213G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406680 | |||||||
| chr6:44406730 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.903+263A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406730 | |||||||
| chr6:44406771 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.903+304G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406771 | |||||||
| chr6:44406792 | A | G | 1 | a0001c0002t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.903+325A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406792 | |||||||
| chr6:44406940 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0135 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.903+473A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406940 | |||||||
| chr6:44406941 | C | A | 2 | a0001c0001t0008g0133 a0001c0002t0002g0150 |
2 | NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.903+474C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406941 | |||||||
| chr6:44406950 | C | A | 106 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(103): Show |
108 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.903+483C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406950 | |||||||
| chr6:44406987 | T | C | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+520T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406987 | |||||||
| chr6:44406992 | C | G | 1 | a0001c0002t0002g0281 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.903+525C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44406992 | |||||||
| chr6:44407261 | T | C | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.903+794T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407261 | |||||||
| chr6:44407312 | A | G | 1 | a0001c0012t0002g0301 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.903+845A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407312 | |||||||
| chr6:44407330 | C | CT | 14 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+878dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 44407330 | ||||||
| chr6:44407350 | C | T | 1 | a0001c0002t0002g0290 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.903+883C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407350 | |||||||
| chr6:44407354 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.903+887G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407354 | |||||||
| chr6:44407358 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.903+891T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407358 | |||||||
| chr6:44407366 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.903+899C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407366 | |||||||
| chr6:44407488 | C | T | 12 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0182 others(9): Show |
13 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-956C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407488 | |||||||
| chr6:44407557 | C | T | 45 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(42): Show |
46 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.904-887C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407557 | |||||||
| chr6:44407610 | G | A | 9 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 others(6): Show |
9 | HG00621.hp2 HG02015.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-834G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407610 | |||||||
| chr6:44407621 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.904-823C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407621 | |||||||
| chr6:44407911 | T | A | 107 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(104): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.904-533T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407911 | |||||||
| chr6:44407936 | C | T | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.904-508C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44407936 | |||||||
| chr6:44408112 | G | A | 1 | a0001c0001t0024g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.904-332G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408112 | |||||||
| chr6:44408182 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.904-262T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408182 | |||||||
| chr6:44408202 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.904-242T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408202 | |||||||
| chr6:44408213 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.904-231A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408213 | |||||||
| chr6:44408230 | A | G | 2 | a0001c0002t0002g0322 a0001c0002t0002g0334 |
2 | HG02132.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.904-214A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408230 | |||||||
| chr6:44408282 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.904-162T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 7/15 | chr6 | 44408282 | |||||||
| chr6:44408847 | A | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+215A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44408847 | |||||||
| chr6:44408912 | T | A | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1092+280T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44408912 | |||||||
| chr6:44409010 | C | T | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+378C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409010 | |||||||
| chr6:44409033 | G | C | 1 | a0001c0003t0010g0338 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1092+401G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409033 | |||||||
| chr6:44409044 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1092+412G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409044 | |||||||
| chr6:44409242 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18970.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1092+610C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409242 | |||||||
| chr6:44409327 | G | A | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1092+695G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409327 | |||||||
| chr6:44409646 | G | A | 1 | a0001c0007t0002g0040 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1092+1014G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409646 | |||||||
| chr6:44409802 | C | T | 1 | a0001c0003t0003g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1092+1170C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44409802 | |||||||
| chr6:44410125 | G | A | 1 | a0001c0004t0009g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1092+1493G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410125 | |||||||
| chr6:44410134 | T | C | 1 | a0001c0004t0004g0010 | 2 | NA18945.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1092+1502T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410134 | |||||||
| chr6:44410156 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1092+1524A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410156 | |||||||
| chr6:44410172 | A | G | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1092+1540A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410172 | |||||||
| chr6:44410233 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1092+1601C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410233 | |||||||
| chr6:44410280 | C | T | 1 | a0001c0003t0003g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1092+1648C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410280 | |||||||
| chr6:44410371 | G | A | 1 | a0001c0003t0010g0338 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1092+1739G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410371 | |||||||
| chr6:44410458 | A | G | 3 | a0001c0003t0010g0161 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1092+1826A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410458 | |||||||
| chr6:44410462 | G | T | 9 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 others(6): Show |
9 | HG00621.hp2 HG02015.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092+1830G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410462 | |||||||
| chr6:44410486 | G | A | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1092+1854G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410486 | |||||||
| chr6:44410635 | C | T | 1 | a0001c0002t0002g0295 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1092+2003C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410635 | |||||||
| chr6:44410719 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1092+2087T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410719 | |||||||
| chr6:44410923 | T | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+2291T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410923 | |||||||
| chr6:44410970 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+2338G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44410970 | |||||||
| chr6:44411185 | A | G | 1 | a0001c0001t0008g0081 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1092+2553A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411185 | |||||||
| chr6:44411432 | T | G | 1 | a0001c0002t0005g0233 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1092+2800T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411432 | |||||||
| chr6:44411465 | AT | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1092+2835delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411465 | ||||||
| chr6:44411555 | G | A | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+2923G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411555 | |||||||
| chr6:44411598 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+2966C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411598 | |||||||
| chr6:44411612 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1092+2980G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411612 | |||||||
| chr6:44411631 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0016g0084 a0001c0001t0016g0137 |
2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1092+3000_1092+300 others(18): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411631 | ||||||
| chr6:44411633 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1092+3002_1092+300 others(14): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411633 | ||||||
| chr6:44411633 | A | AGTGTGTG others(5): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0035 others(6): Show |
10 | HG00673.hp1 HG01884.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1092+3002_1092+300 others(16): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411633 | ||||||
| chr6:44411633 | A | AGTGTGTG others(7): Show |
41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(38): Show |
42 | HG00280.hp1 HG00408.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1092+3002_1092+300 others(18): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411633 | ||||||
| chr6:44411633 | A | AGTGTGTG others(9): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0079 a0001c0001t0030g0098 |
3 | HG00423.hp2 HG02976.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1092+3002_1092+300 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411633 | ||||||
| chr6:44411633 | A | AGTGTGTG others(11): Show |
1 | a0001c0001t0001g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1092+3002_1092+300 others(22): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411633 | ||||||
| chr6:44411633 | A | T | 2 | a0001c0001t0016g0084 a0001c0001t0016g0137 |
2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1092+3001A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411633 | |||||||
| chr6:44411635 | A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
12 | HG00673.hp2 HG01496.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(14): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0024 a0001c0001t0024g0027 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(16): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(7): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
57 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(18): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0071 a0001c0001t0025g0072 |
2 | HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(11): Show |
5 | a0001c0001t0001g0073 a0001c0001t0001g0126 a0001c0001t0023g0336 others(2): Show |
5 | HG02896.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(22): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(13): Show |
32 | a0001c0003t0003g0009 a0001c0003t0003g0157 a0001c0003t0003g0159 others(29): Show |
33 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(24): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(15): Show |
3 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 |
3 | HG00099.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(26): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | AGTGTGTG others(17): Show |
2 | a0001c0003t0003g0168 a0001c0003t0003g0200 |
2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1092+3004_1092+300 others(28): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411635 | ||||||
| chr6:44411635 | A | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
59 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1092+3003A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411635 | |||||||
| chr6:44411637 | A | AGAGAGAG others(43): Show |
2 | a0001c0002t0002g0266 a0001c0002t0002g0307 |
2 | NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(54): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
1 | a0001c0002t0027g0324 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(43): Show |
1 | a0001c0002t0002g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(54): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(45): Show |
1 | a0001c0002t0002g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(56): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
6 | a0001c0002t0002g0012 a0001c0002t0002g0295 a0001c0002t0002g0297 others(3): Show |
7 | HG00733.hp1 HG00735.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(41): Show |
5 | a0001c0002t0002g0271 a0001c0002t0002g0277 a0001c0002t0002g0278 others(2): Show |
5 | HG00408.hp2 HG02074.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(52): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(43): Show |
2 | a0001c0002t0002g0279 a0001c0002t0002g0323 |
2 | NA18979.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(54): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(35): Show |
3 | a0001c0002t0002g0164 a0001c0002t0002g0267 a0001c0002t0029g0333 |
3 | HG04199.hp2 NA18949.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(46): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(37): Show |
7 | a0001c0002t0002g0011 a0001c0002t0002g0272 a0001c0002t0002g0293 others(4): Show |
8 | HG01358.hp1 HG01975.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(48): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
3 | a0001c0002t0002g0290 a0001c0002t0002g0304 a0001c0002t0004g0312 |
3 | HG02735.hp2 NA18946.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(33): Show |
2 | a0001c0002t0002g0322 a0001c0005t0002g0258 |
2 | HG02132.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(44): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(35): Show |
6 | a0001c0002t0002g0150 a0001c0002t0002g0151 a0001c0002t0002g0296 others(3): Show |
6 | HG00423.hp1 NA18612.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(46): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(37): Show |
13 | a0001c0002t0002g0152 a0001c0002t0002g0261 a0001c0002t0002g0263 others(10): Show |
13 | HG02083.hp1 NA18612.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(48): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
2 | a0001c0002t0002g0274 a0001c0002t0002g0275 |
2 | HG02132.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(43): Show |
1 | a0001c0002t0002g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(54): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(25): Show |
1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(36): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(33): Show |
3 | a0001c0002t0002g0268 a0001c0002t0002g0330 a0001c0002t0002g0335 |
3 | HG02135.hp2 HG03831.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(44): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(35): Show |
11 | a0001c0002t0002g0148 a0001c0002t0002g0149 a0001c0002t0002g0262 others(8): Show |
11 | HG00438.hp2 HG01361.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(46): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(37): Show |
4 | a0001c0002t0002g0281 a0001c0002t0002g0317 a0001c0002t0002g0318 others(1): Show |
4 | HG04115.hp1 NA18973.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(48): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
1 | a0001c0002t0015g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(41): Show |
1 | a0001c0002t0002g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(52): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(23): Show |
1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(34): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(29): Show |
2 | a0001c0002t0002g0282 a0001c0002t0002g0289 |
2 | HG02040.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(40): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(31): Show |
4 | a0001c0002t0002g0285 a0001c0002t0002g0319 a0001c0002t0002g0320 others(1): Show |
4 | HG01243.hp1 HG02523.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(42): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(33): Show |
1 | a0001c0002t0002g0303 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(44): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(35): Show |
1 | a0001c0004t0004g0181 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(46): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(39): Show |
1 | a0001c0002t0015g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(50): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(19): Show |
1 | a0001c0002t0011g0321 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(30): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(29): Show |
5 | a0001c0005t0002g0231 a0001c0005t0002g0235 a0001c0005t0002g0236 others(2): Show |
5 | HG00741.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(40): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(31): Show |
3 | a0001c0002t0002g0260 a0001c0002t0002g0291 a0001c0002t0002g0300 |
3 | HG00558.hp1 HG04228.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(42): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(25): Show |
1 | a0001c0002t0005g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(36): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(27): Show |
1 | a0001c0002t0002g0331 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(38): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(29): Show |
2 | a0001c0002t0002g0259 a0001c0005t0031g0257 |
2 | HG02717.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(40): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(21): Show |
4 | a0001c0002t0005g0233 a0001c0002t0005g0234 a0001c0002t0005g0237 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(32): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGAG others(9): Show |
1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGTG others(11): Show |
2 | a0001c0004t0007g0226 a0001c0004t0007g0239 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(22): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGAGTG others(13): Show |
3 | a0001c0004t0007g0227 a0001c0004t0007g0228 a0001c0004t0009g0242 |
3 | HG02486.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(24): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGTGTG others(5): Show |
1 | a0001c0008t0022g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(16): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGTGTG others(11): Show |
2 | a0001c0001t0001g0163 a0001c0003t0010g0338 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(22): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGTGTG others(13): Show |
5 | a0001c0001t0001g0217 a0001c0001t0006g0216 a0001c0004t0004g0017 others(2): Show |
5 | HG00597.hp2 HG01255.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(24): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGTGTG others(15): Show |
9 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0178 others(6): Show |
9 | HG00621.hp2 NA18947.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092+3006_1092+300 others(26): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGAGTGTG others(19): Show |
1 | a0001c0001t0006g0177 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1092+3006_1092+300 others(30): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18970.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1092+3013_1092+302 others(14): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(7): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+3009_1092+302 others(18): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(9): Show |
14 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0046 others(11): Show |
14 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1092+3007_1092+302 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(11): Show |
15 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(12): Show |
16 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.1092+3022_1092+302 others(22): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(13): Show |
2 | a0001c0003t0003g0158 a0001c0003t0003g0208 |
2 | NA18981.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1092+3022_1092+302 others(24): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | AGTGTGTG others(15): Show |
3 | a0001c0003t0003g0156 a0001c0003t0003g0190 a0001c0003t0003g0192 |
3 | HG00280.hp2 HG01109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1092+3022_1092+302 others(26): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411637 | ||||||
| chr6:44411637 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1092+3005A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411637 | |||||||
| chr6:44411718 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+3086C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44411718 | |||||||
| chr6:44411864 | TCCTTGGA others(9): Show |
T | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+3234_1092+324 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44411864 | ||||||
| chr6:44412068 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1092+3436C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412068 | |||||||
| chr6:44412088 | C | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+3456C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412088 | |||||||
| chr6:44412175 | C | T | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1092+3543C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412175 | |||||||
| chr6:44412266 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0132 |
3 | NA18941.hp2 NA18946.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1092+3634A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412266 | |||||||
| chr6:44412308 | CT | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(326): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1092+3689delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44412308 | ||||||
| chr6:44412323 | A | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+3691A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412323 | |||||||
| chr6:44412373 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+3741C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412373 | |||||||
| chr6:44412408 | T | C | 1 | a0001c0001t0024g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1092+3776T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412408 | |||||||
| chr6:44412417 | G | C | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1092+3785G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412417 | |||||||
| chr6:44412422 | C | T | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+3790C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412422 | |||||||
| chr6:44412475 | C | T | 2 | a0001c0002t0004g0309 a0001c0002t0004g0312 |
2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1092+3843C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412475 | |||||||
| chr6:44412602 | G | GT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1092+3980dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44412602 | ||||||
| chr6:44412643 | A | G | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1092+4011A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412643 | |||||||
| chr6:44412739 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+4107C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412739 | |||||||
| chr6:44412781 | C | CT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1092+4168dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44412781 | ||||||
| chr6:44412781 | C | CTT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0082 others(23): Show |
27 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1092+4167_1092+416 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44412781 | ||||||
| chr6:44412869 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1092+4237G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44412869 | |||||||
| chr6:44413028 | C | T | 1 | a0001c0004t0009g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1092+4396C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413028 | |||||||
| chr6:44413060 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0045 others(1): Show |
4 | HG01069.hp1 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+4428G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413060 | |||||||
| chr6:44413194 | C | G | 1 | a0001c0001t0017g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1092+4562C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413194 | |||||||
| chr6:44413204 | T | G | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1092+4572T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413204 | |||||||
| chr6:44413319 | G | A | 3 | a0001c0003t0010g0161 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1092+4687G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413319 | |||||||
| chr6:44413433 | G | A | 3 | a0001c0002t0002g0164 a0001c0002t0002g0296 a0001c0002t0002g0297 |
3 | NA18949.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1092+4801G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413433 | |||||||
| chr6:44413505 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1092+4873A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413505 | |||||||
| chr6:44413575 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1092+4943G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413575 | |||||||
| chr6:44413660 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092+5028C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413660 | |||||||
| chr6:44413708 | C | T | 172 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(169): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1092+5076C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413708 | |||||||
| chr6:44413790 | G | A | 106 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(103): Show |
108 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1092+5158G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44413790 | |||||||
| chr6:44414166 | A | G | 3 | a0001c0004t0004g0017 a0001c0004t0004g0245 a0001c0004t0004g0247 |
3 | HG00597.hp2 NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1093-5283A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414166 | |||||||
| chr6:44414220 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-5229C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414220 | |||||||
| chr6:44414382 | C | CTG | 12 | a0001c0002t0005g0253 a0001c0003t0003g0189 a0001c0003t0003g0192 others(9): Show |
14 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1093-5019_1093-501 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTG | C | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0025 others(32): Show |
37 | HG00673.hp1 HG01496.hp2 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1093-5019_1093-501 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTG | C | 92 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0038 others(89): Show |
94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1093-5021_1093-501 others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTG | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
110 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1093-5023_1093-501 others(10): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(1): Show |
C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(28): Show |
33 | HG00280.hp1 HG00621.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1093-5025_1093-501 others(12): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(3): Show |
C | 2 | a0001c0002t0002g0314 a0001c0002t0011g0321 |
2 | NA18952.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1093-5027_1093-501 others(14): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(5): Show |
C | 7 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(4): Show |
7 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-5029_1093-501 others(16): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(9): Show |
C | 1 | a0001c0002t0002g0272 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1093-5033_1093-501 others(20): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(13): Show |
C | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1093-5037_1093-501 others(24): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414382 | CTGTGTGT others(15): Show |
C | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1093-5039_1093-501 others(26): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44414382 | ||||||
| chr6:44414396 | G | T | 1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1093-5053G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414396 | |||||||
| chr6:44414426 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1093-5023G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414426 | |||||||
| chr6:44414428 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1093-5021G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414428 | |||||||
| chr6:44414430 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1093-5019G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414430 | |||||||
| chr6:44414432 | A | T | 3 | a0001c0001t0001g0044 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG02630.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1093-5017A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414432 | |||||||
| chr6:44414705 | C | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-4744C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414705 | |||||||
| chr6:44414744 | T | A | 3 | a0001c0004t0004g0017 a0001c0004t0004g0245 a0001c0004t0004g0247 |
3 | HG00597.hp2 NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1093-4705T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414744 | |||||||
| chr6:44414882 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1093-4567T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44414882 | |||||||
| chr6:44415185 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1093-4264G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415185 | |||||||
| chr6:44415219 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1093-4230G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415219 | |||||||
| chr6:44415265 | G | A | 1 | a0001c0002t0005g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1093-4184G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415265 | |||||||
| chr6:44415393 | G | C | 43 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(40): Show |
44 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1093-4056G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415393 | |||||||
| chr6:44415530 | G | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-3919G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415530 | |||||||
| chr6:44415731 | C | T | 1 | a0001c0002t0002g0264 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1093-3718C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415731 | |||||||
| chr6:44415859 | G | A | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1093-3590G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415859 | |||||||
| chr6:44415880 | T | G | 1 | a0001c0002t0002g0151 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1093-3569T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415880 | |||||||
| chr6:44415964 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1093-3485A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415964 | |||||||
| chr6:44415991 | G | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0136 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093-3458G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44415991 | |||||||
| chr6:44416151 | A | G | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1093-3298A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44416151 | |||||||
| chr6:44416364 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1093-3085T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44416364 | |||||||
| chr6:44416502 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-2947A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44416502 | |||||||
| chr6:44416823 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-2626T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44416823 | |||||||
| chr6:44416961 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG01496.hp1 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-2488C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44416961 | |||||||
| chr6:44417072 | G | A | 55 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(52): Show |
57 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1093-2377G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417072 | |||||||
| chr6:44417096 | A | C | 102 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(99): Show |
104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1093-2353A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417096 | |||||||
| chr6:44417344 | G | C | 54 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(51): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1093-2105G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417344 | |||||||
| chr6:44417513 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-1936C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417513 | |||||||
| chr6:44417608 | C | T | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1093-1841C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417608 | |||||||
| chr6:44417704 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0051 others(5): Show |
8 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1093-1745A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417704 | |||||||
| chr6:44417879 | C | G | 1 | a0001c0004t0007g0241 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1093-1570C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417879 | |||||||
| chr6:44417933 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1093-1516G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44417933 | |||||||
| chr6:44418101 | C | T | 1 | a0001c0002t0002g0308 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1093-1348C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418101 | |||||||
| chr6:44418102 | C | G | 1 | a0001c0002t0002g0308 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1093-1347C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418102 | |||||||
| chr6:44418125 | C | T | 1 | a0001c0002t0002g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1093-1324C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418125 | |||||||
| chr6:44418209 | T | C | 1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1093-1240T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418209 | |||||||
| chr6:44418216 | G | A | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1093-1233G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418216 | |||||||
| chr6:44418243 | G | A | 5 | a0001c0002t0005g0233 a0001c0002t0005g0234 a0001c0002t0005g0237 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-1206G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418243 | |||||||
| chr6:44418356 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0136 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093-1093A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418356 | |||||||
| chr6:44418371 | T | C | 5 | a0001c0006t0012g0002 a0001c0008t0022g0144 a0001c0009t0001g0145 others(2): Show |
7 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1093-1078T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418371 | |||||||
| chr6:44418459 | G | A | 1 | a0001c0002t0002g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1093-990G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418459 | |||||||
| chr6:44418504 | A | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-945A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418504 | |||||||
| chr6:44418583 | C | T | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1093-866C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418583 | |||||||
| chr6:44418613 | G | A | 4 | a0001c0002t0002g0291 a0001c0003t0010g0161 a0001c0010t0033g0153 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-836G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418613 | |||||||
| chr6:44418632 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-817A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418632 | |||||||
| chr6:44418656 | C | CTGT | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-791_1093-789d others(5): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44418656 | ||||||
| chr6:44418679 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1093-770T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418679 | |||||||
| chr6:44418840 | T | G | 1 | a0001c0003t0003g0171 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1093-609T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418840 | |||||||
| chr6:44418845 | G | GT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1093-590dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44418845 | ||||||
| chr6:44418845 | G | GTT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0034 others(3): Show |
6 | HG01981.hp2 HG03492.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-591_1093-590d others(4): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 44418845 | ||||||
| chr6:44418845 | G | T | 5 | a0001c0005t0002g0231 a0001c0005t0002g0235 a0001c0005t0002g0236 others(2): Show |
5 | HG00741.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093-604G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418845 | |||||||
| chr6:44418922 | C | T | 5 | a0001c0001t0016g0084 a0001c0001t0016g0137 a0001c0002t0002g0149 others(2): Show |
5 | HG01255.hp2 HG03139.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-527C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418922 | |||||||
| chr6:44418934 | C | T | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1093-515C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44418934 | |||||||
| chr6:44419017 | T | G | 1 | a0001c0003t0003g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1093-432T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44419017 | |||||||
| chr6:44419403 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1093-46T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 8/15 | chr6 | 44419403 | |||||||
| chr6:44419778 | C | T | 1 | a0001c0004t0007g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241+181C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44419778 | |||||||
| chr6:44419780 | C | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1241+183C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44419780 | |||||||
| chr6:44419834 | C | T | 2 | a0001c0001t0017g0167 a0001c0001t0017g0199 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1241+237C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44419834 | |||||||
| chr6:44419853 | C | A | 170 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(167): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1241+256C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44419853 | |||||||
| chr6:44419973 | T | G | 1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1241+376T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44419973 | |||||||
| chr6:44420079 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1241+482A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420079 | |||||||
| chr6:44420208 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0097 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1241+611C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420208 | |||||||
| chr6:44420211 | G | A | 1 | a0001c0002t0015g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1241+614G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420211 | |||||||
| chr6:44420380 | C | T | 5 | a0001c0002t0002g0259 a0001c0002t0002g0260 a0001c0002t0002g0302 others(2): Show |
5 | HG00423.hp1 HG02559.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241+783C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420380 | |||||||
| chr6:44420406 | T | C | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241+809T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420406 | |||||||
| chr6:44420604 | C | T | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1241+1007C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420604 | |||||||
| chr6:44420701 | C | T | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241+1104C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420701 | |||||||
| chr6:44420768 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1241+1171G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420768 | |||||||
| chr6:44420850 | G | A | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1241+1253G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44420850 | |||||||
| chr6:44421005 | T | C | 1 | a0001c0001t0003g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1241+1408T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421005 | |||||||
| chr6:44421014 | G | A | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241+1417G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421014 | |||||||
| chr6:44421027 | G | A | 1 | a0001c0002t0002g0297 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1241+1430G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421027 | |||||||
| chr6:44421032 | C | T | 1 | a0001c0004t0004g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1241+1435C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421032 | |||||||
| chr6:44421103 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | NA18994.hp2 NA18997.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1241+1506A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421103 | |||||||
| chr6:44421133 | T | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG01496.hp1 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1242-1514T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421133 | |||||||
| chr6:44421215 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1242-1432G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421215 | |||||||
| chr6:44421250 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1242-1397G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421250 | |||||||
| chr6:44421310 | T | A | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1242-1337T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421310 | |||||||
| chr6:44421437 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1242-1210G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421437 | |||||||
| chr6:44421450 | A | C | 16 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1242-1197A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421450 | |||||||
| chr6:44421662 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1242-985A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421662 | |||||||
| chr6:44421694 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1242-953G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421694 | |||||||
| chr6:44421757 | A | T | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1242-890A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421757 | |||||||
| chr6:44421829 | G | T | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1242-818G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421829 | |||||||
| chr6:44421864 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0097 others(1): Show |
4 | HG02735.hp1 HG02818.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-783C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421864 | |||||||
| chr6:44421906 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1242-741A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421906 | |||||||
| chr6:44421929 | G | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1242-718G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421929 | |||||||
| chr6:44421990 | G | A | 1 | a0001c0003t0003g0187 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1242-657G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44421990 | |||||||
| chr6:44422349 | A | T | 1 | a0002c0015t0013g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1242-298A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44422349 | |||||||
| chr6:44422373 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1242-274G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44422373 | |||||||
| chr6:44422392 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1242-255G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44422392 | |||||||
| chr6:44422553 | A | G | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1242-94A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 9/15 | chr6 | 44422553 | |||||||
| chr6:44423027 | G | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
16 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1404+218G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44423027 | |||||||
| chr6:44423202 | G | A | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1404+393G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44423202 | |||||||
| chr6:44423465 | C | T | 1 | a0001c0004t0019g0193 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1404+656C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44423465 | |||||||
| chr6:44423746 | A | G | 2 | a0001c0001t0017g0167 a0001c0001t0017g0199 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1405-673A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44423746 | |||||||
| chr6:44423780 | A | T | 1 | a0001c0001t0024g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1405-639A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44423780 | |||||||
| chr6:44424022 | G | T | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1405-397G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44424022 | |||||||
| chr6:44424162 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1405-257G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44424162 | |||||||
| chr6:44424279 | A | C | 5 | a0001c0002t0005g0233 a0001c0002t0005g0234 a0001c0002t0005g0237 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-140A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44424279 | |||||||
| chr6:44424340 | T | C | 1 | a0001c0003t0003g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1405-79T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 10/15 | chr6 | 44424340 | |||||||
| chr6:44424724 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1569+141T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44424724 | |||||||
| chr6:44424777 | G | A | 183 | a0001c0001t0001g0162 a0001c0001t0003g0057 a0001c0001t0003g0058 others(180): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1569+194G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44424777 | |||||||
| chr6:44424922 | A | G | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+339A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44424922 | |||||||
| chr6:44424942 | C | T | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1569+359C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44424942 | |||||||
| chr6:44424971 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+388C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44424971 | |||||||
| chr6:44425031 | T | C | 2 | a0001c0002t0002g0322 a0001c0002t0002g0334 |
2 | HG02132.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1569+448T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425031 | |||||||
| chr6:44425044 | A | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+461A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425044 | |||||||
| chr6:44425068 | G | C | 8 | a0001c0005t0002g0231 a0001c0005t0002g0232 a0001c0005t0002g0235 others(5): Show |
8 | HG00741.hp1 HG01243.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1569+485G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425068 | |||||||
| chr6:44425256 | A | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1569+673A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425256 | |||||||
| chr6:44425515 | A | G | 3 | a0001c0003t0010g0161 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1570-588A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425515 | |||||||
| chr6:44425526 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1570-577A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425526 | |||||||
| chr6:44425530 | CAG | C | 105 | a0001c0001t0008g0023 a0001c0001t0008g0076 a0001c0001t0008g0077 others(102): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1570-572_1570-571d others(4): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425530 | |||||||
| chr6:44425895 | A | T | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570-208A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425895 | |||||||
| chr6:44425898 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
16 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1570-205G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425898 | |||||||
| chr6:44425974 | A | G | 1 | a0001c0003t0003g0202 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1570-129A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 11/15 | chr6 | 44425974 | |||||||
| chr6:44426228 | T | C | 11 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(8): Show |
11 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1650+45T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 12/15 | chr6 | 44426228 | |||||||
| chr6:44426381 | T | A | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1651-101T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 12/15 | chr6 | 44426381 | |||||||
| chr6:44426472 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1651-10A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 12/15 | chr6 | 44426472 | |||||||
| chr6:44427530 | G | C | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893+806G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427530 | |||||||
| chr6:44427567 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1893+843C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427567 | |||||||
| chr6:44427624 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1893+900T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427624 | |||||||
| chr6:44427629 | A | G | 56 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(53): Show |
58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1893+905A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427629 | |||||||
| chr6:44427640 | A | G | 1 | a0001c0001t0006g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1893+916A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427640 | |||||||
| chr6:44427669 | G | C | 1 | a0001c0008t0022g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1893+945G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44427669 | |||||||
| chr6:44427690 | G | GT | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893+967dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 44427690 | ||||||
| chr6:44428004 | A | G | 2 | a0001c0004t0009g0250 a0001c0004t0009g0252 |
2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1893+1280A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428004 | |||||||
| chr6:44428041 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0135 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1893+1317A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428041 | |||||||
| chr6:44428217 | C | CT | 10 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 others(7): Show |
10 | HG00621.hp2 HG02015.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1894-1493dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 44428217 | ||||||
| chr6:44428250 | T | C | 1 | a0001c0001t0014g0125 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1894-1463T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428250 | |||||||
| chr6:44428303 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1894-1410C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428303 | |||||||
| chr6:44428316 | A | C | 7 | a0001c0002t0002g0230 a0001c0002t0002g0281 a0001c0002t0002g0282 others(4): Show |
7 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894-1397A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428316 | |||||||
| chr6:44428364 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1894-1349G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428364 | |||||||
| chr6:44428574 | A | G | 1 | a0001c0003t0003g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1894-1139A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428574 | |||||||
| chr6:44428779 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1894-934C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44428779 | |||||||
| chr6:44429015 | C | CT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0034 others(40): Show |
45 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1894-674dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 44429015 | ||||||
| chr6:44429015 | CT | C | 23 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0046 others(20): Show |
23 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1894-674delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 44429015 | ||||||
| chr6:44429015 | CTT | C | 12 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(9): Show |
14 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1894-675_1894-674d others(4): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 44429015 | ||||||
| chr6:44429039 | T | G | 1 | a0001c0002t0002g0306 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1894-674T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429039 | |||||||
| chr6:44429145 | C | T | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-568C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429145 | |||||||
| chr6:44429176 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1894-537T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429176 | |||||||
| chr6:44429278 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1894-435C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429278 | |||||||
| chr6:44429544 | G | C | 56 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(53): Show |
58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1894-169G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429544 | |||||||
| chr6:44429593 | C | T | 1 | a0001c0005t0002g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1894-120C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 13/15 | chr6 | 44429593 | |||||||
| chr6:44430085 | T | G | 1 | a0001c0002t0002g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2091+175T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430085 | |||||||
| chr6:44430139 | A | G | 1 | a0001c0002t0002g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2091+229A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430139 | |||||||
| chr6:44430145 | T | C | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2091+235T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430145 | |||||||
| chr6:44430146 | G | C | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+236G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430146 | |||||||
| chr6:44430511 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2091+601G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430511 | |||||||
| chr6:44430576 | C | CT | 12 | a0001c0001t0001g0095 a0001c0001t0001g0129 a0001c0001t0001g0217 others(9): Show |
12 | HG01255.hp1 HG02723.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.2091+681dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44430576 | ||||||
| chr6:44430722 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+812C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44430722 | |||||||
| chr6:44431059 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2091+1149A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44431059 | |||||||
| chr6:44431440 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0110 |
2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2091+1530A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44431440 | |||||||
| chr6:44431452 | T | G | 201 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(198): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2091+1542T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44431452 | |||||||
| chr6:44431453 | A | G | 201 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(198): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2091+1543A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44431453 | |||||||
| chr6:44431600 | CT | C | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+1696delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44431600 | ||||||
| chr6:44431738 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0110 |
3 | HG00099.hp1 HG02055.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2091+1828T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44431738 | |||||||
| chr6:44432229 | G | T | 168 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(165): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2091+2319G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432229 | |||||||
| chr6:44432305 | T | C | 2 | a0001c0003t0003g0197 a0001c0003t0003g0202 |
2 | HG00323.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2091+2395T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432305 | |||||||
| chr6:44432357 | A | G | 1 | a0001c0002t0002g0262 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2091+2447A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432357 | |||||||
| chr6:44432362 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2091+2452A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432362 | |||||||
| chr6:44432521 | TA | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
22 | HG00673.hp2 HG01069.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2091+2623delA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44432521 | ||||||
| chr6:44432522 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2091+2612A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432522 | |||||||
| chr6:44432540 | G | C | 6 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(3): Show |
6 | HG00673.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091+2630G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432540 | |||||||
| chr6:44432853 | AG | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2091+2944delG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432853 | |||||||
| chr6:44432870 | G | T | 1 | a0001c0003t0003g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2091+2960G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432870 | |||||||
| chr6:44432892 | A | G | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2091+2982A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432892 | |||||||
| chr6:44432917 | T | A | 218 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(215): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.2091+3007T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432917 | |||||||
| chr6:44432975 | A | T | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2091+3065A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44432975 | |||||||
| chr6:44433037 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2091+3127A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433037 | |||||||
| chr6:44433127 | T | C | 1 | a0001c0002t0002g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2091+3217T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433127 | |||||||
| chr6:44433267 | G | C | 100 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(97): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2091+3357G>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433267 | |||||||
| chr6:44433335 | C | G | 16 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2091+3425C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433335 | |||||||
| chr6:44433434 | A | G | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2091+3524A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433434 | |||||||
| chr6:44433488 | G | A | 2 | a0001c0003t0010g0337 a0001c0003t0010g0338 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2091+3578G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433488 | |||||||
| chr6:44433564 | C | T | 202 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(199): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.2091+3654C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433564 | |||||||
| chr6:44433642 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2091+3732T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433642 | |||||||
| chr6:44433696 | A | G | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2091+3786A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433696 | |||||||
| chr6:44433923 | G | A | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2091+4013G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44433923 | |||||||
| chr6:44434167 | C | T | 5 | a0001c0004t0004g0181 a0001c0004t0004g0182 a0001c0004t0004g0183 others(2): Show |
5 | NA18964.hp2 NA18984.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2091+4257C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434167 | |||||||
| chr6:44434283 | T | A | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2091+4373T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434283 | |||||||
| chr6:44434322 | A | C | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2091+4412A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434322 | |||||||
| chr6:44434391 | TG | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2091+4482delG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434391 | |||||||
| chr6:44434394 | G | A | 202 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(199): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.2091+4484G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434394 | |||||||
| chr6:44434621 | G | A | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2091+4711G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434621 | |||||||
| chr6:44434651 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2091+4741T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434651 | |||||||
| chr6:44434957 | G | A | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2091+5047G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44434957 | |||||||
| chr6:44435078 | C | G | 1 | a0001c0001t0001g0022 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2091+5168C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435078 | |||||||
| chr6:44435111 | CT | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0127 a0001c0002t0002g0315 others(2): Show |
7 | HG00280.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091+5215delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44435111 | ||||||
| chr6:44435170 | C | T | 11 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(8): Show |
11 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.2091+5260C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435170 | |||||||
| chr6:44435298 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2091+5388G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435298 | |||||||
| chr6:44435376 | A | C | 1 | a0001c0003t0003g0159 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2091+5466A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435376 | |||||||
| chr6:44435664 | T | A | 1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2091+5754T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435664 | |||||||
| chr6:44435701 | A | G | 203 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(200): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.2091+5791A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435701 | |||||||
| chr6:44435787 | G | GT | 106 | a0001c0001t0001g0042 a0001c0002t0002g0011 a0001c0002t0002g0012 others(103): Show |
108 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2091+5889dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44435787 | ||||||
| chr6:44435793 | T | G | 1 | a0001c0009t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2091+5883T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435793 | |||||||
| chr6:44435862 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0041 |
2 | HG00733.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2091+5952A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435862 | |||||||
| chr6:44435939 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2091+6029G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435939 | |||||||
| chr6:44435980 | A | G | 1 | a0001c0002t0005g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2091+6070A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44435980 | |||||||
| chr6:44436039 | A | G | 16 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2091+6129A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436039 | |||||||
| chr6:44436048 | G | A | 5 | a0001c0004t0009g0242 a0001c0004t0009g0249 a0001c0004t0009g0250 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091+6138G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436048 | |||||||
| chr6:44436107 | G | T | 1 | a0001c0002t0011g0321 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2091+6197G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436107 | |||||||
| chr6:44436134 | A | T | 2 | a0001c0008t0022g0144 a0001c0009t0001g0145 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2091+6224A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436134 | |||||||
| chr6:44436163 | G | T | 202 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(199): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.2091+6253G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436163 | |||||||
| chr6:44436279 | T | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0059 others(2): Show |
5 | HG02630.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091+6369T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436279 | |||||||
| chr6:44436334 | G | A | 241 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0024 others(238): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2091+6424G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436334 | |||||||
| chr6:44436338 | T | G | 171 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(168): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2091+6428T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436338 | |||||||
| chr6:44436425 | C | CATT | 229 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(226): Show |
235 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.2091+6515_2091+651 others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436425 | |||||||
| chr6:44436645 | A | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+6735A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436645 | |||||||
| chr6:44436781 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2091+6871G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436781 | |||||||
| chr6:44436783 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2091+6873G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436783 | |||||||
| chr6:44436809 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2091+6899C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436809 | |||||||
| chr6:44436851 | G | T | 1 | a0001c0003t0003g0211 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2091+6941G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436851 | |||||||
| chr6:44436918 | C | G | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+7008C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436918 | |||||||
| chr6:44436967 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2091+7057T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436967 | |||||||
| chr6:44436977 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2091+7067A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44436977 | |||||||
| chr6:44437139 | A | T | 2 | a0001c0005t0002g0236 a0001c0005t0002g0255 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2091+7229A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437139 | |||||||
| chr6:44437371 | G | A | 1 | a0001c0010t0033g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2091+7461G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437371 | |||||||
| chr6:44437471 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0026 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2091+7561T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437471 | |||||||
| chr6:44437516 | G | T | 16 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2091+7606G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437516 | |||||||
| chr6:44437590 | G | T | 199 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(196): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.2091+7680G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437590 | |||||||
| chr6:44437615 | A | G | 13 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0181 others(10): Show |
14 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.2091+7705A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437615 | |||||||
| chr6:44437772 | T | C | 1 | a0001c0003t0003g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2091+7862T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437772 | |||||||
| chr6:44437822 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2092-7833G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437822 | |||||||
| chr6:44437962 | T | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-7693T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437962 | |||||||
| chr6:44437986 | GT | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-7667delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44437986 | ||||||
| chr6:44437994 | G | T | 13 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0181 others(10): Show |
14 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-7661G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44437994 | |||||||
| chr6:44438010 | C | T | 13 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0181 others(10): Show |
14 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-7645C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438010 | |||||||
| chr6:44438035 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0103 others(1): Show |
4 | HG03209.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092-7620C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438035 | |||||||
| chr6:44438038 | C | T | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-7617C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438038 | |||||||
| chr6:44438069 | C | G | 1 | a0001c0001t0017g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2092-7586C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438069 | |||||||
| chr6:44438150 | A | C | 1 | a0001c0002t0002g0266 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2092-7505A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438150 | |||||||
| chr6:44438207 | C | G | 17 | a0001c0002t0002g0012 a0001c0002t0002g0164 a0001c0002t0002g0273 others(14): Show |
18 | HG00733.hp1 HG00735.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2092-7448C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438207 | |||||||
| chr6:44438339 | A | G | 1 | a0001c0005t0002g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2092-7316A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438339 | |||||||
| chr6:44438361 | T | C | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-7294T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438361 | |||||||
| chr6:44438378 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-7277G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438378 | |||||||
| chr6:44438408 | A | C | 3 | a0001c0003t0010g0161 a0001c0003t0010g0337 a0001c0003t0010g0338 |
3 | HG01884.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2092-7247A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438408 | |||||||
| chr6:44438458 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-7197A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438458 | |||||||
| chr6:44438570 | A | G | 2 | a0001c0002t0002g0276 a0001c0002t0002g0305 |
2 | NA18994.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2092-7085A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438570 | |||||||
| chr6:44438665 | C | CT | 6 | a0001c0001t0001g0022 a0001c0001t0001g0114 a0001c0002t0002g0164 others(3): Show |
8 | HG02451.hp2 HG02976.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.2092-6968dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44438665 | ||||||
| chr6:44438665 | CT | C | 28 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0068 others(25): Show |
28 | HG00323.hp1 HG00639.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.2092-6968delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44438665 | ||||||
| chr6:44438665 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0006g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2092-6977_2092-696 others(14): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44438665 | ||||||
| chr6:44438732 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2092-6923G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438732 | |||||||
| chr6:44438809 | C | T | 1 | a0001c0003t0010g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2092-6846C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438809 | |||||||
| chr6:44438943 | T | G | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2092-6712T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44438943 | |||||||
| chr6:44439050 | A | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG01496.hp1 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2092-6605A>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439050 | |||||||
| chr6:44439115 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-6540G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439115 | |||||||
| chr6:44439171 | A | G | 219 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(216): Show |
225 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.2092-6484A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439171 | |||||||
| chr6:44439179 | A | G | 11 | a0001c0001t0001g0217 a0001c0001t0006g0175 a0001c0001t0006g0176 others(8): Show |
11 | HG00621.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.2092-6476A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439179 | |||||||
| chr6:44439331 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-6324C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439331 | |||||||
| chr6:44439419 | G | GA | 102 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(99): Show |
104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2092-6232dupA | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44439419 | ||||||
| chr6:44439532 | A | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(12): Show |
15 | HG01069.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2092-6123A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439532 | |||||||
| chr6:44439796 | T | C | 5 | a0001c0002t0005g0233 a0001c0002t0005g0234 a0001c0002t0005g0237 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.2092-5859T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439796 | |||||||
| chr6:44439889 | A | T | 1 | a0001c0003t0003g0209 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2092-5766A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439889 | |||||||
| chr6:44439934 | C | A | 1 | a0001c0002t0002g0334 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2092-5721C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44439934 | |||||||
| chr6:44440127 | A | G | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-5528A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440127 | |||||||
| chr6:44440130 | G | GTT | 3 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0126 |
3 | HG02055.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2092-5522_2092-552 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44440130 | ||||||
| chr6:44440160 | T | C | 69 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(66): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2092-5495T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440160 | |||||||
| chr6:44440452 | AG | A | 69 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(66): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2092-5201delG | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44440452 | ||||||
| chr6:44440493 | G | T | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2092-5162G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440493 | |||||||
| chr6:44440608 | AT | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(12): Show |
15 | HG01069.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2092-5041delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44440608 | ||||||
| chr6:44440627 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-5028G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440627 | |||||||
| chr6:44440663 | C | T | 13 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0181 others(10): Show |
14 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-4992C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440663 | |||||||
| chr6:44440708 | C | CT | 26 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00423.hp2 HG00673.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2092-4930dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44440708 | ||||||
| chr6:44440708 | CT | C | 75 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(72): Show |
77 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2092-4930delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44440708 | ||||||
| chr6:44440827 | C | T | 1 | a0001c0011t0002g0166 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2092-4828C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440827 | |||||||
| chr6:44440871 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2092-4784C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440871 | |||||||
| chr6:44440923 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-4732G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44440923 | |||||||
| chr6:44441145 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2092-4510A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441145 | |||||||
| chr6:44441148 | C | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-4507C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441148 | |||||||
| chr6:44441241 | A | G | 203 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(200): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.2092-4414A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441241 | |||||||
| chr6:44441416 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2092-4239C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441416 | |||||||
| chr6:44441425 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-4230G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441425 | |||||||
| chr6:44441449 | T | A | 1 | a0001c0002t0002g0313 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2092-4206T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441449 | |||||||
| chr6:44441514 | C | T | 65 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(62): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2092-4141C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441514 | |||||||
| chr6:44441552 | G | A | 14 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(11): Show |
14 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-4103G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441552 | |||||||
| chr6:44441577 | A | G | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-4078A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441577 | |||||||
| chr6:44441793 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2092-3862T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441793 | |||||||
| chr6:44441805 | G | A | 8 | a0001c0005t0002g0231 a0001c0005t0002g0232 a0001c0005t0002g0235 others(5): Show |
8 | HG00741.hp1 HG01243.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2092-3850G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441805 | |||||||
| chr6:44441844 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2092-3811T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441844 | |||||||
| chr6:44441849 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2092-3806T>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441849 | |||||||
| chr6:44441851 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2092-3804T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441851 | |||||||
| chr6:44441891 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2092-3764T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441891 | |||||||
| chr6:44441932 | C | CT | 83 | a0001c0001t0001g0127 a0001c0001t0001g0217 a0001c0001t0005g0154 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2092-3700dupT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44441932 | ||||||
| chr6:44441932 | C | CTT | 40 | a0001c0001t0001g0163 a0001c0001t0006g0216 a0001c0001t0017g0167 others(37): Show |
41 | HG00733.hp1 HG00735.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.2092-3701_2092-370 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44441932 | ||||||
| chr6:44441932 | C | CTTT | 58 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(55): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2092-3702_2092-370 others(7): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44441932 | ||||||
| chr6:44441932 | C | CTTTT | 9 | a0001c0003t0003g0169 a0001c0003t0003g0192 a0001c0003t0003g0200 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.2092-3703_2092-370 others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44441932 | ||||||
| chr6:44441932 | C | T | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2092-3723C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441932 | |||||||
| chr6:44441932 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0097 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2092-3710_2092-370 others(15): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44441932 | ||||||
| chr6:44441965 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2092-3690C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44441965 | |||||||
| chr6:44442023 | A | G | 203 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(200): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.2092-3632A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442023 | |||||||
| chr6:44442061 | C | T | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2092-3594C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442061 | |||||||
| chr6:44442062 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2092-3593G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442062 | |||||||
| chr6:44442252 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0111 |
2 | NA18978.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2092-3403T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442252 | |||||||
| chr6:44442312 | A | G | 3 | a0001c0001t0006g0216 a0001c0002t0002g0269 a0001c0002t0002g0279 |
3 | HG02258.hp1 NA18995.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2092-3343A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442312 | |||||||
| chr6:44442375 | T | TTG | 34 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0031 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2092-3246_2092-324 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442375 | T | TTGTG | 16 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0033 others(13): Show |
16 | HG00621.hp2 HG01069.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.2092-3248_2092-324 others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442375 | T | TTGTGTG | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0102 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2092-3250_2092-324 others(10): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442375 | TTG | T | 28 | a0001c0001t0001g0069 a0001c0001t0001g0119 a0001c0001t0001g0162 others(25): Show |
29 | HG00597.hp2 HG00741.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2092-3246_2092-324 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442375 | TTGTG | T | 55 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(52): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2092-3248_2092-324 others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442375 | TTGTGTG | T | 11 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(8): Show |
13 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.2092-3250_2092-324 others(10): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44442375 | ||||||
| chr6:44442459 | C | G | 101 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0148 others(98): Show |
103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2092-3196C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442459 | |||||||
| chr6:44442459 | CTT | C | 4 | a0001c0001t0001g0162 a0001c0001t0005g0155 a0001c0001t0005g0194 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-3195_2092-319 others(6): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442459 | |||||||
| chr6:44442766 | G | A | 1 | a0001c0004t0009g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2092-2889G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442766 | |||||||
| chr6:44442783 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0111 |
2 | NA18978.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2092-2872G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44442783 | |||||||
| chr6:44443009 | GT | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.2092-2637delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44443009 | ||||||
| chr6:44443083 | C | T | 2 | a0001c0004t0004g0010 a0001c0004t0004g0243 |
3 | NA18945.hp1 NA18985.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2092-2572C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443083 | |||||||
| chr6:44443098 | TTTCC | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-2545_2092-254 others(8): Show |
CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44443098 | ||||||
| chr6:44443254 | G | A | 1 | a0001c0003t0003g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2092-2401G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443254 | |||||||
| chr6:44443406 | G | A | 2 | a0001c0004t0019g0160 a0001c0004t0019g0193 |
2 | HG00673.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2092-2249G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443406 | |||||||
| chr6:44443482 | G | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-2173G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443482 | |||||||
| chr6:44443645 | A | G | 1 | a0001c0013t0032g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2092-2010A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443645 | |||||||
| chr6:44443672 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2092-1983A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443672 | |||||||
| chr6:44443755 | G | A | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092-1900G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443755 | |||||||
| chr6:44443795 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2092-1860G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443795 | |||||||
| chr6:44443806 | T | C | 13 | a0001c0004t0004g0010 a0001c0004t0004g0017 a0001c0004t0004g0181 others(10): Show |
14 | HG00597.hp2 NA18945.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-1849T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443806 | |||||||
| chr6:44443864 | G | T | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-1791G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44443864 | |||||||
| chr6:44444000 | A | T | 1 | a0001c0003t0003g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2092-1655A>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444000 | |||||||
| chr6:44444106 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2092-1549A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444106 | |||||||
| chr6:44444115 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-1540G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444115 | |||||||
| chr6:44444211 | A | G | 207 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0136 others(204): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.2092-1444A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444211 | |||||||
| chr6:44444255 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0097 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2092-1400C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444255 | |||||||
| chr6:44444557 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0097 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2092-1098T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444557 | |||||||
| chr6:44444655 | CT | C | 16 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0006g0175 others(13): Show |
16 | HG00621.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2092-996delT | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr6 | 44444655 | ||||||
| chr6:44444667 | G | A | 1 | a0001c0002t0002g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2092-988G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444667 | |||||||
| chr6:44444895 | C | T | 2 | a0001c0001t0017g0167 a0001c0001t0017g0199 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2092-760C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444895 | |||||||
| chr6:44444944 | G | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2092-711G>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444944 | |||||||
| chr6:44444949 | C | T | 1 | a0001c0002t0011g0321 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2092-706C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44444949 | |||||||
| chr6:44445035 | C | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0136 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092-620C>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44445035 | |||||||
| chr6:44445320 | C | A | 1 | a0001c0002t0005g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2092-335C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44445320 | |||||||
| chr6:44445389 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2092-266G>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44445389 | |||||||
| chr6:44445403 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0131 |
2 | NA19054.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2092-252C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44445403 | |||||||
| chr6:44445575 | C | T | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2092-80C>T | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 14/15 | chr6 | 44445575 | |||||||
| chr6:44445924 | C | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2304+57C>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44445924 | |||||||
| chr6:44445925 | T | A | 1 | a0001c0006t0012g0002 | 3 | HG02451.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2304+58T>A | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44445925 | |||||||
| chr6:44445945 | A | G | 4 | a0001c0001t0005g0154 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2304+78A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44445945 | |||||||
| chr6:44445999 | A | G | 171 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0112 others(168): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2304+132A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44445999 | |||||||
| chr6:44446207 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2304+340T>C | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44446207 | |||||||
| chr6:44446348 | A | G | 2 | a0001c0010t0033g0153 a0001c0013t0032g0146 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2305-259A>G | CDC5L | ENSG00000096401.8 | transcript | ENST00000371477.4 | protein_coding | 15/15 | chr6 | 44446348 |