Item | Value |
---|---|
geneid | 9907 |
ensemblid | ENSG00000242802.9 |
hgncid | 22197 |
symbol | AP5Z1 |
name | adaptor related protein complex 5 subunit zeta 1 |
refseq_nuc | NM_014855.3 |
refseq_prot | NP_055670.1 |
ensembl_nuc | ENST00000649063.2 |
ensembl_prot | ENSP00000497815.1 |
mane_status | MANE Select |
chr | chr7 |
start | 4775623 |
end | 4794397 |
strand | + |
ver | v1.2 |
region | chr7:4775623-4794397 |
region5000 | chr7:4770623-4799397 |
regionname0 | AP5Z1_chr7_4775623_4794397 |
regionname5000 | AP5Z1_chr7_4770623_4799397 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 807 | 258 | 62 | 52 | 99 | 12 | 31 | 74 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0002 | 0/0 | 807 | 31 | 2 | 2 | 14 | 0 | 13 | 11 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0003 | 0/0 | 803 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(798): Show |
chr7 | 4770623 | 4799397 |
a0004 | 0/0 | 807 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0005 | 0/0 | 803 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(798): Show |
chr7 | 4770623 | 4799397 |
a0006 | 0/0 | 807 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0007 | 0/0 | 807 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0008 | 0/0 | 807 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0009 | 0/0 | 807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0010 | 0/0 | 803 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(798): Show |
chr7 | 4770623 | 4799397 |
a0011 | 0/0 | 807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0012 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0013 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0014 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0015 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0016 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0017 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0018 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0019 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(798): Show |
chr7 | 4770623 | 4799397 |
a0020 | 0/0 | 807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0021 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
a0022 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | MFSAG others(802): Show |
chr7 | 4770623 | 4799397 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2421 | 203 | 18 | 48 | 96 | 10 | 29 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0002 | 0/0 | 2421 | 36 | 31 | 2 | 0 | 2 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0005 | 0/0 | 2421 | 6 | 4 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0006 | 0/0 | 2421 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0014 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0020 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0021 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0024 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0025 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0001c0027 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0002c0003 | 0/0 | 2421 | 29 | 2 | 2 | 13 | 0 | 12 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0002c0030 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0002c0033 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0003c0004 | 0/0 | 2409 | 19 | 17 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2404): Show |
chr7 | 4770623 | 4799397 | ||
a0004c0007 | 0/0 | 2421 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0005c0011 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2404): Show |
chr7 | 4770623 | 4799397 | ||
a0005c0018 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2404): Show |
chr7 | 4770623 | 4799397 | ||
a0006c0008 | 0/0 | 2421 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0007c0009 | 0/0 | 2421 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0008c0034 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0008c0035 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0009c0012 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0010c0013 | 0/0 | 2409 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2404): Show |
chr7 | 4770623 | 4799397 | ||
a0011c0010 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0012c0019 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0013c0023 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0014c0028 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0015c0031 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0016c0015 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0017c0026 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0018c0017 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0019c0029 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2404): Show |
chr7 | 4770623 | 4799397 | ||
a0020c0016 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0021c0022 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 | ||
a0022c0032 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | ATGTT others(2416): Show |
chr7 | 4770623 | 4799397 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5529 | 159 | 3 | 38 | 87 | 8 | 21 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0002 | 0/0 | 5545 | 8 | 7 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0005 | 0/0 | 5529 | 12 | 0 | 6 | 1 | 1 | 4 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0006 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0008 | 0/0 | 5529 | 4 | 0 | 0 | 2 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0010 | 0/0 | 5529 | 4 | 1 | 1 | 1 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0014 | 0/0 | 5529 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0016 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0022 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0026 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0028 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0030 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0034 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0035 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0037 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0039 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0040 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0041 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0001c0001t0049 | 0/0 | 5528 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0001 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0002 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0003 | 0/0 | 5529 | 15 | 13 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0006 | 0/0 | 5529 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0015 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0017 | 0/0 | 5528 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0018 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0027 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0031 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0032 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5526): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0033 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5526): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0036 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0038 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0002t0044 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0005t0009 | 0/0 | 5528 | 5 | 3 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0001c0005t0048 | 0/0 | 5528 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0001c0006t0003 | 0/0 | 5529 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0014t0006 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0014t0029 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0020t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0021t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0024t0001 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0025t0006 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0001c0027t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0002c0003t0002 | 0/0 | 5545 | 24 | 2 | 2 | 9 | 0 | 11 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0002c0003t0011 | 0/0 | 5545 | 4 | 0 | 0 | 4 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0002c0003t0043 | 0/0 | 5545 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0002c0030t0002 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0002c0033t0002 | 0/0 | 5545 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5540): Show |
chr7 | 4770623 | 4799397 |
a0003c0004t0004 | 0/0 | 5517 | 14 | 14 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5512): Show |
chr7 | 4770623 | 4799397 |
a0003c0004t0007 | 0/0 | 5517 | 5 | 3 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5512): Show |
chr7 | 4770623 | 4799397 |
a0004c0007t0012 | 0/0 | 5528 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0005c0011t0007 | 0/0 | 5517 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5512): Show |
chr7 | 4770623 | 4799397 |
a0005c0018t0019 | 0/0 | 5517 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5512): Show |
chr7 | 4770623 | 4799397 |
a0006c0008t0013 | 0/0 | 5523 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5518): Show |
chr7 | 4770623 | 4799397 |
a0007c0009t0001 | 0/0 | 5529 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0008c0034t0001 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0008c0035t0042 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0009c0012t0007 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0009c0012t0046 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0010c0013t0021 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5551): Show |
chr7 | 4770623 | 4799397 |
a0010c0013t0045 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5551): Show |
chr7 | 4770623 | 4799397 |
a0011c0010t0023 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0011c0010t0025 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0012c0019t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0013c0023t0001 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0014c0028t0047 | 0/0 | 5528 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5523): Show |
chr7 | 4770623 | 4799397 |
a0015c0031t0001 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0016c0015t0008 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0017c0026t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0018c0017t0024 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0019c0029t0020 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5552): Show |
chr7 | 4770623 | 4799397 |
a0020c0016t0001 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0021c0022t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
a0022c0032t0001 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | GACGC others(5524): Show |
chr7 | 4770623 | 4799397 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 51 | 2 | 16 | 20 | 3 | 9 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0048 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0005g0005 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0008g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0010g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0014g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0016g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0026g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0028g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0030g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0034g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0035g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0039g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0040g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0041g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0001t0049g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0017 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0006g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0017g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0018g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0027g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0031g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0032g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0033g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0036g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0038g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0002t0044g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0005t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0005t0009g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0005t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0005t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0005t0048g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0006t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0006t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0006t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0014t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0014t0029g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0021t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0025t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0001c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0004 | 0/0 | 9 | 0 | 0 | 5 | 0 | 4 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0011g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0003t0043g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0030t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0002c0033t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0004g0003 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0007g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0003c0004t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0004c0007t0012g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0004c0007t0012g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0005c0011t0007g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0005c0018t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0006c0008t0013g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0006c0008t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0007c0009t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0008c0034t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0008c0035t0042g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0009c0012t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0009c0012t0046g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0010c0013t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0010c0013t0045g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0011c0010t0023g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0011c0010t0025g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0012c0019t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0013c0023t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0014c0028t0047g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0015c0031t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0016c0015t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0017c0026t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0018c0017t0024g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0019c0029t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0020c0016t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0021c0022t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
a0022c0032t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0109 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00280 | hp1 | a0001 | c0001 | t0010 | g0019 | EUR | FIN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00597 | hp1 | a0002 | c0003 | t0011 | g0025 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00609 | hp2 | a0012 | c0019 | t0001 | g0103 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01070 | hp2 | a0003 | c0004 | t0007 | g0072 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01071 | hp1 | a0003 | c0004 | t0007 | g0016 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0157 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01074 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01081 | hp1 | a0001 | c0005 | t0009 | g0030 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01081 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0013 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01169 | hp1 | a0001 | c0001 | t0014 | g0153 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01175 | hp1 | a0001 | c0002 | t0017 | g0024 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0068 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01243 | hp2 | a0005 | c0011 | t0007 | g0027 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01261 | hp2 | a0002 | c0003 | t0002 | g0047 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01358 | hp1 | a0008 | c0034 | t0001 | g0126 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01361 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01433 | hp1 | a0013 | c0023 | t0001 | g0020 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01496 | hp1 | a0001 | c0005 | t0009 | g0031 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01496 | hp2 | a0014 | c0028 | t0047 | g0085 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01515 | hp1 | a0001 | c0002 | t0017 | g0024 | EUR | IBS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01884 | hp2 | a0001 | c0005 | t0048 | g0030 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01891 | hp2 | a0006 | c0008 | t0013 | g0032 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01952 | hp1 | a0015 | c0031 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02055 | hp1 | a0001 | c0002 | t0006 | g0088 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02055 | hp2 | a0001 | c0025 | t0006 | g0010 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02074 | hp2 | a0002 | c0003 | t0002 | g0004 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02083 | hp1 | a0016 | c0015 | t0008 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02132 | hp1 | a0008 | c0035 | t0042 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02145 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02155 | hp2 | a0017 | c0026 | t0001 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02257 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02257 | hp2 | a0001 | c0002 | t0015 | g0078 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02258 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02280 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02280 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02451 | hp1 | a0005 | c0018 | t0019 | g0052 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02451 | hp2 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02523 | hp2 | a0001 | c0020 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02572 | hp1 | a0003 | c0004 | t0004 | g0054 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02572 | hp2 | a0001 | c0002 | t0038 | g0012 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02615 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02622 | hp1 | a0001 | c0001 | t0028 | g0001 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02622 | hp2 | a0003 | c0004 | t0004 | g0067 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02630 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02630 | hp2 | a0001 | c0005 | t0009 | g0031 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02647 | hp1 | a0001 | c0002 | t0015 | g0049 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0004 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02717 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0056 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02738 | hp2 | a0001 | c0001 | t0022 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02809 | hp1 | a0001 | c0006 | t0003 | g0074 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02886 | hp2 | a0006 | c0008 | t0013 | g0086 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02896 | hp1 | a0001 | c0002 | t0006 | g0089 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02896 | hp2 | a0001 | c0002 | t0018 | g0028 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02897 | hp1 | a0001 | c0002 | t0018 | g0028 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02897 | hp2 | a0009 | c0012 | t0007 | g0003 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02922 | hp1 | a0010 | c0013 | t0021 | g0029 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02922 | hp2 | a0001 | c0014 | t0006 | g0090 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02965 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02970 | hp1 | a0009 | c0012 | t0046 | g0161 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02976 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03041 | hp1 | a0006 | c0008 | t0013 | g0032 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03041 | hp2 | a0001 | c0002 | t0027 | g0080 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03139 | hp1 | a0001 | c0002 | t0033 | g0069 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03139 | hp2 | a0018 | c0017 | t0024 | g0091 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03195 | hp1 | a0001 | c0005 | t0009 | g0083 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03195 | hp2 | a0003 | c0004 | t0004 | g0003 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03209 | hp1 | a0001 | c0001 | t0049 | g0082 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03209 | hp2 | a0001 | c0005 | t0009 | g0084 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03225 | hp1 | a0002 | c0003 | t0002 | g0059 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03225 | hp2 | a0010 | c0013 | t0045 | g0029 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0004 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03453 | hp1 | a0001 | c0014 | t0029 | g0087 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03486 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0071 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03491 | hp1 | a0004 | c0007 | t0012 | g0065 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03491 | hp2 | a0002 | c0003 | t0002 | g0026 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0026 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03516 | hp1 | a0003 | c0004 | t0004 | g0003 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03516 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03540 | hp2 | a0001 | c0002 | t0032 | g0077 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03579 | hp2 | a0001 | c0002 | t0031 | g0058 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0061 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0004 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03688 | hp1 | a0002 | c0003 | t0002 | g0060 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03704 | hp2 | a0020 | c0016 | t0001 | g0128 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03710 | hp1 | a0001 | c0024 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0062 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0004 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03927 | hp2 | a0002 | c0033 | t0002 | g0047 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03942 | hp2 | a0001 | c0001 | t0040 | g0013 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0063 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04184 | hp1 | a0002 | c0003 | t0043 | g0025 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18522 | hp2 | a0011 | c0010 | t0023 | g0033 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18747 | hp2 | a0002 | c0003 | t0002 | g0004 | EAS | CHB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18906 | hp1 | a0003 | c0004 | t0007 | g0095 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18906 | hp2 | a0005 | c0011 | t0007 | g0027 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18940 | hp1 | a0002 | c0003 | t0002 | g0004 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18942 | hp2 | a0002 | c0003 | t0011 | g0004 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18947 | hp2 | a0021 | c0022 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18951 | hp1 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18951 | hp2 | a0002 | c0003 | t0002 | g0004 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18954 | hp2 | a0001 | c0001 | t0030 | g0038 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18960 | hp1 | a0001 | c0001 | t0034 | g0156 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18960 | hp2 | a0022 | c0032 | t0001 | g0021 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0004 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18966 | hp1 | a0001 | c0021 | t0001 | g0131 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18967 | hp2 | a0001 | c0001 | t0026 | g0138 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18975 | hp1 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19009 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19030 | hp1 | a0001 | c0001 | t0041 | g0113 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0023 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19043 | hp1 | a0001 | c0001 | t0035 | g0150 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19043 | hp2 | a0003 | c0004 | t0004 | g0003 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19057 | hp2 | a0002 | c0003 | t0002 | g0055 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19064 | hp1 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19066 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19070 | hp2 | a0002 | c0030 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19083 | hp2 | a0001 | c0001 | t0039 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19085 | hp1 | a0002 | c0003 | t0011 | g0004 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19086 | hp2 | a0002 | c0003 | t0011 | g0057 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19089 | hp1 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19091 | hp1 | a0001 | c0027 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19091 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19240 | hp1 | a0003 | c0004 | t0004 | g0066 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA19240 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ASW | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20129 | hp2 | a0003 | c0004 | t0007 | g0016 | AFR | ASW | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0017 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | GIH | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02109 | hp1 | a0001 | c0002 | t0044 | g0079 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02109 | hp2 | a0001 | c0002 | t0036 | g0051 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02486 | hp2 | a0002 | c0003 | t0002 | g0098 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG02559 | hp2 | a0003 | c0004 | t0004 | g0003 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03471 | hp1 | a0019 | c0029 | t0020 | g0076 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG03471 | hp2 | a0003 | c0004 | t0007 | g0016 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0023 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20300 | hp1 | a0011 | c0010 | t0025 | g0033 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
NA21309 | hp2 | a0001 | c0006 | t0003 | g0075 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0048 | REF | REF | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | AP5Z1_chr7_4770623_4799397 | AP5Z1 | chr7 | 4770623 | 4799397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4781188 | G | A | 1 | a0016 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.55G>A | p.Glu19Lys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/17 | 148/5529 | 55/2424 | 19/807 | chr7 | 4781188 | |||
chr7:4781297 | C | T | 1 | a0008 | 2 | HG01358.hp1 HG02132.hp1 |
missense_variant | MODERATE | c.164C>T | p.Thr55Met | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/17 | 257/5529 | 164/2424 | 55/807 | chr7 | 4781297 | |||
chr7:4781669 | C | G | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.281C>G | p.Ser94Cys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 374/5529 | 281/2424 | 94/807 | chr7 | 4781669 | |||
chr7:4781717 | G | A | 1 | a0020 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.329G>A | p.Arg110Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 422/5529 | 329/2424 | 110/807 | chr7 | 4781717 | |||
chr7:4781721 | G | C | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.333G>C | p.Gln111His | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 426/5529 | 333/2424 | 111/807 | chr7 | 4781721 | |||
chr7:4783328 | G | A | 1 | a0005 | 3 | HG01243.hp2 HG02451.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.379G>A | p.Glu127Lys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 472/5529 | 379/2424 | 127/807 | chr7 | 4783328 | |||
chr7:4783439 | A | G | 1 | a0022 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.490A>G | p.Ser164Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 583/5529 | 490/2424 | 164/807 | chr7 | 4783439 | |||
chr7:4783761 | A | G | 1 | a0007 | 3 | NA18951.hp1 NA18975.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.584A>G | p.His195Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 677/5529 | 584/2424 | 195/807 | chr7 | 4783761 | |||
chr7:4783784 | C | T | 1 | a0015 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.607C>T | p.Pro203Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 700/5529 | 607/2424 | 203/807 | chr7 | 4783784 | |||
chr7:4784264 | G | C | 1 | a0012 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.683G>C | p.Ser228Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 776/5529 | 683/2424 | 228/807 | chr7 | 4784264 | |||
chr7:4784354 | C | T | 1 | a0014 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.773C>T | p.Pro258Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 866/5529 | 773/2424 | 258/807 | chr7 | 4784354 | |||
chr7:4785676 | T | A | 1 | a0002 | 31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
missense_variant | MODERATE | c.1124T>A | p.Leu375Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/17 | 1217/5529 | 1124/2424 | 375/807 | chr7 | 4785676 | |||
chr7:4787707 | C | G | 1 | a0019 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1385C>G | p.Thr462Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1478/5529 | 1385/2424 | 462/807 | chr7 | 4787707 | |||
chr7:4788162 | C | T | 1 | a0017 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1463C>T | p.Pro488Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1556/5529 | 1463/2424 | 488/807 | chr7 | 4788162 | |||
chr7:4788222 | C | G | 1 | a0010 | 2 | HG02922.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1523C>G | p.Ala508Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1616/5529 | 1523/2424 | 508/807 | chr7 | 4788222 | |||
chr7:4788228 | G | A | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.1529G>A | p.Arg510Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1622/5529 | 1529/2424 | 510/807 | chr7 | 4788228 | |||
chr7:4790763 | C | G | 1 | a0018 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.2029C>G | p.Leu677Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2122/5529 | 2029/2424 | 677/807 | chr7 | 4790763 | |||
chr7:4790817 | C | A | 1 | a0021 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.2083C>A | p.Pro695Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2176/5529 | 2083/2424 | 695/807 | chr7 | 4790817 | |||
chr7:4790832 | G | A | 1 | a0013 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2098G>A | p.Val700Met | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2191/5529 | 2098/2424 | 700/807 | chr7 | 4790832 | |||
chr7:4791165 | CCAGCTCC others(5): Show |
C | 4 | a0003 a0005 a0010 others(1): Show |
25 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(22): Show |
conservative_inframe_deletion | MODERATE | c.2209_2220delTCCACG others(6): Show |
p.Ser737_Ser740del | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2302/5529 | 2209/2424 | 737/807 | INFO_REALIGN_3_PRIME | chr7 | 4791165 | ||
chr7:4791191 | G | A | 3 | a0009 a0010 a0019 |
5 | HG02897.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.2230G>A | p.Ala744Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2323/5529 | 2230/2424 | 744/807 | chr7 | 4791191 | |||
chr7:4791266 | A | G | 1 | a0006 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2305A>G | p.Thr769Ala | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2398/5529 | 2305/2424 | 769/807 | chr7 | 4791266 | |||
chr7:4791289 | C | A | 2 | a0011 a0018 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.2328C>A | p.Ser776Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2421/5529 | 2328/2424 | 776/807 | chr7 | 4791289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4783318 | T | C | 2 | a0011c0010 a0018c0017 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
splice_region_variant&synonymous_variant | LOW | c.369T>C | p.Gly123Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 462/5529 | 369/2424 | 123/807 | chr7 | 4783318 | |||
chr7:4783393 | C | G | 1 | a0002c0033 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.444C>G | p.Pro148Pro | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 537/5529 | 444/2424 | 148/807 | chr7 | 4783393 | |||
chr7:4783765 | C | T | 2 | a0008c0035 a0022c0032 |
2 | HG02132.hp1 NA18960.hp2 |
synonymous_variant | LOW | c.588C>T | p.Ser196Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 681/5529 | 588/2424 | 196/807 | chr7 | 4783765 | |||
chr7:4784256 | G | C | 1 | a0018c0017 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.675G>C | p.Val225Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 768/5529 | 675/2424 | 225/807 | chr7 | 4784256 | |||
chr7:4784340 | C | T | 13 | a0001c0002 a0001c0006 a0001c0014 others(10): Show |
103 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(100): Show |
synonymous_variant | LOW | c.759C>T | p.Ser253Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 852/5529 | 759/2424 | 253/807 | chr7 | 4784340 | |||
chr7:4784367 | C | T | 1 | a0001c0027 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 879/5529 | 786/2424 | 262/807 | chr7 | 4784367 | |||
chr7:4784951 | C | T | 1 | a0002c0030 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.834C>T | p.Ser278Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/17 | 927/5529 | 834/2424 | 278/807 | chr7 | 4784951 | |||
chr7:4785683 | C | T | 3 | a0002c0003 a0002c0030 a0002c0033 |
31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
splice_region_variant&synonymous_variant | LOW | c.1131C>T | p.His377His | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/17 | 1224/5529 | 1131/2424 | 377/807 | chr7 | 4785683 | |||
chr7:4786314 | G | A | 1 | a0004c0007 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
synonymous_variant | LOW | c.1197G>A | p.Glu399Glu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/17 | 1290/5529 | 1197/2424 | 399/807 | chr7 | 4786314 | |||
chr7:4786353 | G | A | 1 | a0001c0020 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1236G>A | p.Gln412Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/17 | 1329/5529 | 1236/2424 | 412/807 | chr7 | 4786353 | |||
chr7:4787637 | C | T | 1 | a0006c0008 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.1315C>T | p.Leu439Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1408/5529 | 1315/2424 | 439/807 | chr7 | 4787637 | |||
chr7:4787691 | C | T | 1 | a0001c0006 | 6 | HG02717.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
synonymous_variant | LOW | c.1369C>T | p.Leu457Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1462/5529 | 1369/2424 | 457/807 | chr7 | 4787691 | |||
chr7:4787699 | C | T | 4 | a0001c0014 a0002c0003 a0002c0030 others(1): Show |
33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
synonymous_variant | LOW | c.1377C>T | p.Asp459Asp | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1470/5529 | 1377/2424 | 459/807 | chr7 | 4787699 | |||
chr7:4788253 | C | T | 2 | a0001c0005 a0014c0028 |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.1554C>T | p.Phe518Phe | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1647/5529 | 1554/2424 | 518/807 | chr7 | 4788253 | |||
chr7:4788256 | A | G | 2 | a0010c0013 a0019c0029 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1557A>G | p.Gln519Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1650/5529 | 1557/2424 | 519/807 | chr7 | 4788256 | |||
chr7:4788262 | G | A | 1 | a0010c0013 | 2 | HG02922.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.1563G>A | p.Leu521Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1656/5529 | 1563/2424 | 521/807 | chr7 | 4788262 | |||
chr7:4790795 | T | C | 1 | a0001c0021 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.2061T>C | p.Ser687Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2154/5529 | 2061/2424 | 687/807 | chr7 | 4790795 | |||
chr7:4790825 | G | T | 1 | a0001c0025 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2091G>T | p.Val697Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2184/5529 | 2091/2424 | 697/807 | chr7 | 4790825 | |||
chr7:4791193 | G | A | 1 | a0001c0024 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.2232G>A | p.Ala744Ala | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2325/5529 | 2232/2424 | 744/807 | chr7 | 4791193 | |||
chr7:4791340 | G | T | 1 | a0004c0007 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
synonymous_variant | LOW | c.2379G>T | p.Thr793Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2472/5529 | 2379/2424 | 793/807 | chr7 | 4791340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4775713 | G | A | 1 | a0005c0018t0019 | 1 | HG02451.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-3G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/17 | chr7 | 4775713 | |||||||
chr7:4775715 | G | C | 3 | a0006c0008t0013 a0010c0013t0021 a0019c0029t0020 |
5 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/17 | 1 | chr7 | 4775715 | ||||||
chr7:4791430 | A | G | 9 | a0001c0001t0049 a0001c0002t0017 a0001c0002t0018 others(6): Show |
20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 45 | chr7 | 4791430 | ||||||
chr7:4791453 | G | A | 1 | a0003c0004t0004 | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 68 | chr7 | 4791453 | ||||||
chr7:4791526 | C | G | 2 | a0010c0013t0021 a0010c0013t0045 |
2 | HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 141 | chr7 | 4791526 | ||||||
chr7:4791533 | G | A | 1 | a0001c0001t0022 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 148 | chr7 | 4791533 | ||||||
chr7:4791535 | G | A | 3 | a0011c0010t0023 a0011c0010t0025 a0018c0017t0024 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*150G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 150 | chr7 | 4791535 | ||||||
chr7:4791540 | TG | T | 3 | a0009c0012t0046 a0010c0013t0021 a0010c0013t0045 |
3 | HG02922.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*157delG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 157 | INFO_REALIGN_3_PRIME | chr7 | 4791540 | |||||
chr7:4791543 | C | A | 3 | a0009c0012t0046 a0010c0013t0021 a0010c0013t0045 |
3 | HG02922.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 158 | chr7 | 4791543 | ||||||
chr7:4791546 | C | T | 1 | a0011c0010t0025 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 161 | chr7 | 4791546 | ||||||
chr7:4791574 | G | A | 1 | a0001c0001t0026 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 189 | chr7 | 4791574 | ||||||
chr7:4791590 | G | A | 14 | a0001c0001t0028 a0001c0002t0027 a0003c0004t0004 others(11): Show |
32 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 205 | chr7 | 4791590 | ||||||
chr7:4791596 | ACTGAG | A | 1 | a0006c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*222_*226delCTGAG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 222 | INFO_REALIGN_3_PRIME | chr7 | 4791596 | |||||
chr7:4791635 | T | G | 5 | a0001c0001t0049 a0001c0002t0017 a0001c0005t0009 others(2): Show |
10 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 250 | chr7 | 4791635 | ||||||
chr7:4791661 | T | C | 7 | a0001c0001t0049 a0001c0002t0017 a0001c0005t0009 others(4): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*276T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 276 | chr7 | 4791661 | ||||||
chr7:4791763 | T | C | 7 | a0001c0001t0049 a0001c0002t0017 a0001c0005t0009 others(4): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 378 | chr7 | 4791763 | ||||||
chr7:4791817 | C | G | 1 | a0006c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*432C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 432 | chr7 | 4791817 | ||||||
chr7:4791825 | G | A | 1 | a0001c0014t0029 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 440 | chr7 | 4791825 | ||||||
chr7:4791869 | G | A | 1 | a0001c0001t0014 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*484G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 484 | chr7 | 4791869 | ||||||
chr7:4791916 | G | A | 2 | a0011c0010t0023 a0011c0010t0025 |
2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*531G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 531 | chr7 | 4791916 | ||||||
chr7:4791922 | G | A | 1 | a0006c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*537G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 537 | chr7 | 4791922 | ||||||
chr7:4792044 | G | A | 2 | a0001c0001t0010 a0001c0001t0030 |
5 | HG00280.hp1 HG01168.hp1 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 659 | chr7 | 4792044 | ||||||
chr7:4792050 | T | C | 5 | a0003c0004t0004 a0003c0004t0007 a0005c0011t0007 others(2): Show |
23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*665T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 665 | chr7 | 4792050 | ||||||
chr7:4792075 | A | G | 1 | a0001c0001t0016 | 2 | HG06807.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 690 | chr7 | 4792075 | ||||||
chr7:4792119 | G | C | 1 | a0006c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*734G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 734 | chr7 | 4792119 | ||||||
chr7:4792146 | G | A | 11 | a0001c0001t0049 a0001c0002t0015 a0001c0002t0027 others(8): Show |
21 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*761G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 761 | chr7 | 4792146 | ||||||
chr7:4792150 | C | G | 9 | a0003c0004t0004 a0003c0004t0007 a0005c0011t0007 others(6): Show |
27 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*765C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 765 | chr7 | 4792150 | ||||||
chr7:4792158 | G | A | 1 | a0001c0001t0034 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 773 | chr7 | 4792158 | ||||||
chr7:4792241 | G | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 856 | chr7 | 4792241 | ||||||
chr7:4792278 | T | C | 1 | a0001c0001t0035 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 893 | chr7 | 4792278 | ||||||
chr7:4792282 | G | A | 1 | a0014c0028t0047 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*897G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 897 | chr7 | 4792282 | ||||||
chr7:4792286 | C | T | 3 | a0001c0002t0015 a0001c0002t0027 a0001c0002t0044 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*901C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 901 | chr7 | 4792286 | ||||||
chr7:4792304 | CT | C | 7 | a0001c0001t0049 a0001c0002t0017 a0001c0005t0009 others(4): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*921delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 921 | INFO_REALIGN_3_PRIME | chr7 | 4792304 | |||||
chr7:4792307 | C | T | 6 | a0002c0003t0043 a0003c0004t0004 a0003c0004t0007 others(3): Show |
24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 922 | chr7 | 4792307 | ||||||
chr7:4792336 | T | C | 1 | a0001c0002t0031 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 951 | chr7 | 4792336 | ||||||
chr7:4792338 | T | C | 20 | a0001c0001t0049 a0001c0002t0017 a0001c0002t0036 others(17): Show |
48 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*953T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 953 | chr7 | 4792338 | ||||||
chr7:4792424 | G | C | 4 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(1): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1039G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1039 | chr7 | 4792424 | ||||||
chr7:4792424 | G | T | 2 | a0004c0007t0012 a0006c0008t0013 |
7 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1039G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1039 | chr7 | 4792424 | ||||||
chr7:4792479 | G | A | 1 | a0006c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1094G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1094 | chr7 | 4792479 | ||||||
chr7:4792517 | G | A | 1 | a0001c0001t0037 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1132 | chr7 | 4792517 | ||||||
chr7:4792518 | CG | C | 4 | a0009c0012t0046 a0010c0013t0021 a0010c0013t0045 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1136delG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1136 | INFO_REALIGN_3_PRIME | chr7 | 4792518 | |||||
chr7:4792567 | C | T | 5 | a0003c0004t0004 a0003c0004t0007 a0005c0011t0007 others(2): Show |
23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1182 | chr7 | 4792567 | ||||||
chr7:4792572 | G | A | 3 | a0011c0010t0023 a0011c0010t0025 a0018c0017t0024 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1187 | chr7 | 4792572 | ||||||
chr7:4792643 | C | T | 1 | a0008c0035t0042 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1258 | chr7 | 4792643 | ||||||
chr7:4792650 | C | A | 1 | a0001c0002t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1265 | chr7 | 4792650 | ||||||
chr7:4792740 | G | A | 5 | a0001c0002t0003 a0001c0002t0018 a0001c0002t0031 others(2): Show |
25 | HG01243.hp1 HG02109.hp2 HG02559.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1355 | chr7 | 4792740 | ||||||
chr7:4792826 | C | T | 4 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(1): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1441C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1441 | chr7 | 4792826 | ||||||
chr7:4792888 | C | A | 2 | a0011c0010t0023 a0011c0010t0025 |
2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1503C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1503 | chr7 | 4792888 | ||||||
chr7:4792890 | C | T | 17 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(14): Show |
44 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1505 | chr7 | 4792890 | ||||||
chr7:4792940 | C | G | 5 | a0003c0004t0004 a0003c0004t0007 a0005c0011t0007 others(2): Show |
23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1555C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1555 | chr7 | 4792940 | ||||||
chr7:4792979 | C | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1594 | chr7 | 4792979 | ||||||
chr7:4793026 | A | C | 3 | a0011c0010t0023 a0011c0010t0025 a0018c0017t0024 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1641 | chr7 | 4793026 | ||||||
chr7:4793072 | T | C | 18 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(15): Show |
45 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1687T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1687 | chr7 | 4793072 | ||||||
chr7:4793086 | C | G | 17 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(14): Show |
44 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1701C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1701 | chr7 | 4793086 | ||||||
chr7:4793179 | C | T | 3 | a0011c0010t0023 a0011c0010t0025 a0018c0017t0024 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1794C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1794 | chr7 | 4793179 | ||||||
chr7:4793362 | C | T | 1 | a0001c0001t0030 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1977C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1977 | chr7 | 4793362 | ||||||
chr7:4793389 | C | T | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2004 | chr7 | 4793389 | ||||||
chr7:4793398 | C | T | 3 | a0010c0013t0021 a0010c0013t0045 a0019c0029t0020 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2013C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2013 | chr7 | 4793398 | ||||||
chr7:4793468 | A | AGC | 3 | a0001c0002t0032 a0001c0002t0033 a0009c0012t0046 |
3 | HG02970.hp1 HG03139.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085dupGC | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2086 | INFO_REALIGN_3_PRIME | chr7 | 4793468 | |||||
chr7:4793478 | A | G | 8 | a0001c0001t0049 a0001c0002t0015 a0001c0002t0044 others(5): Show |
18 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2093A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2093 | chr7 | 4793478 | ||||||
chr7:4793552 | G | A | 2 | a0001c0001t0008 a0016c0015t0008 |
5 | HG02083.hp1 HG02155.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2167G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2167 | chr7 | 4793552 | ||||||
chr7:4793557 | C | T | 1 | a0001c0001t0049 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2172C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2172 | chr7 | 4793557 | ||||||
chr7:4793582 | A | G | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2197 | chr7 | 4793582 | ||||||
chr7:4793583 | G | C | 3 | a0011c0010t0023 a0011c0010t0025 a0018c0017t0024 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2198G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2198 | chr7 | 4793583 | ||||||
chr7:4793594 | G | GCGTGGGC others(9): Show |
9 | a0001c0001t0002 a0001c0001t0028 a0001c0001t0041 others(6): Show |
42 | HG00597.hp1 HG01074.hp1 HG01109.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2211_*2226dupGTGG others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2227 | INFO_REALIGN_3_PRIME | chr7 | 4793594 | |||||
chr7:4793607 | G | A | 2 | a0011c0010t0023 a0011c0010t0025 |
2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2222 | chr7 | 4793607 | ||||||
chr7:4793613 | C | T | 9 | a0001c0001t0002 a0001c0001t0028 a0001c0001t0041 others(6): Show |
42 | HG00597.hp1 HG01074.hp1 HG01109.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2228 | chr7 | 4793613 | ||||||
chr7:4793629 | G | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2244G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2244 | chr7 | 4793629 | ||||||
chr7:4793671 | G | A | 5 | a0003c0004t0004 a0003c0004t0007 a0005c0011t0007 others(2): Show |
23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2286G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2286 | chr7 | 4793671 | ||||||
chr7:4793687 | G | A | 1 | a0018c0017t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2302G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2302 | chr7 | 4793687 | ||||||
chr7:4793691 | G | A | 2 | a0010c0013t0021 a0010c0013t0045 |
2 | HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2306G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2306 | chr7 | 4793691 | ||||||
chr7:4793719 | C | T | 3 | a0001c0001t0041 a0011c0010t0023 a0011c0010t0025 |
3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2334C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2334 | chr7 | 4793719 | ||||||
chr7:4793722 | C | T | 1 | a0001c0001t0040 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2337C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2337 | chr7 | 4793722 | ||||||
chr7:4793757 | T | G | 1 | a0001c0001t0039 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2372 | chr7 | 4793757 | ||||||
chr7:4793789 | C | T | 1 | a0018c0017t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2404C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2404 | chr7 | 4793789 | ||||||
chr7:4793885 | C | T | 2 | a0001c0002t0015 a0001c0002t0033 |
3 | HG02257.hp2 HG02647.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2500C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2500 | chr7 | 4793885 | ||||||
chr7:4793886 | G | A | 2 | a0001c0001t0049 a0001c0005t0009 |
6 | HG01081.hp1 HG01496.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2501 | chr7 | 4793886 | ||||||
chr7:4793984 | T | C | 4 | a0001c0001t0049 a0001c0005t0009 a0001c0005t0048 others(1): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2599T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2599 | chr7 | 4793984 | ||||||
chr7:4794008 | A | C | 46 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(43): Show |
134 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2623A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2623 | chr7 | 4794008 | ||||||
chr7:4794021 | T | TCTGTATC others(34): Show |
3 | a0010c0013t0021 a0010c0013t0045 a0019c0029t0020 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2637_*2677dupCTGT others(37): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2678 | INFO_REALIGN_3_PRIME | chr7 | 4794021 | |||||
chr7:4794104 | C | A | 3 | a0010c0013t0021 a0010c0013t0045 a0019c0029t0020 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2719C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2719 | chr7 | 4794104 | ||||||
chr7:4794197 | C | T | 1 | a0002c0003t0011 | 4 | HG00597.hp1 NA18942.hp2 NA19085.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2812C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2812 | chr7 | 4794197 | ||||||
chr7:4794226 | A | G | 3 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0040 |
15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2841A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2841 | chr7 | 4794226 | ||||||
chr7:4794234 | G | T | 3 | a0001c0005t0009 a0001c0005t0048 a0014c0028t0047 |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2849G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2849 | chr7 | 4794234 | ||||||
chr7:4794243 | G | C | 3 | a0010c0013t0021 a0010c0013t0045 a0019c0029t0020 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2858G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2858 | chr7 | 4794243 | ||||||
chr7:4794267 | A | G | 7 | a0001c0002t0015 a0001c0002t0017 a0001c0002t0027 others(4): Show |
9 | HG01175.hp1 HG01515.hp1 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2882A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2882 | chr7 | 4794267 | ||||||
chr7:4794367 | G | A | 1 | a0001c0001t0035 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2982G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2982 | chr7 | 4794367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4775757 | G | C | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | splice_donor_variant&intron_variant | HIGH | c.41+1G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775757 | |||||||
chr7:4775843 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0050 |
3 | HG01433.hp2 HG01952.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.41+87G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775843 | |||||||
chr7:4775873 | C | T | 1 | a0009c0012t0046g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41+117C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775873 | |||||||
chr7:4775879 | C | A | 1 | a0001c0001t0016g0023 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.41+123C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775879 | |||||||
chr7:4775897 | T | G | 75 | a0001c0001t0002g0010 a0001c0001t0002g0053 a0001c0001t0006g0010 others(72): Show |
118 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(115): Show |
intron_variant | MODIFIER | c.41+141T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775897 | |||||||
chr7:4775910 | C | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.41+154C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775910 | |||||||
chr7:4775972 | T | C | 75 | a0001c0001t0002g0010 a0001c0001t0002g0053 a0001c0001t0006g0010 others(72): Show |
118 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(115): Show |
intron_variant | MODIFIER | c.41+216T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775972 | |||||||
chr7:4776041 | C | G | 9 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(6): Show |
11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.41+285C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776041 | |||||||
chr7:4776197 | C | CGTGGGAG others(36): Show |
2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+444_41+486dupGG others(41): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776197 | ||||||
chr7:4776355 | T | C | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+599T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776355 | |||||||
chr7:4776441 | G | T | 6 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(3): Show |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+685G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776441 | |||||||
chr7:4776507 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.41+751A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776507 | |||||||
chr7:4776551 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.41+795T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776551 | |||||||
chr7:4776562 | C | CA | 12 | a0001c0001t0001g0018 a0001c0001t0001g0092 a0001c0001t0001g0093 others(9): Show |
13 | HG01981.hp1 HG02027.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+829dupA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776562 | CA | C | 18 | a0001c0001t0001g0021 a0001c0001t0001g0154 a0001c0001t0001g0155 others(15): Show |
21 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+829delA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776562 | CAA | C | 21 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(18): Show |
36 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.41+828_41+829delAA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776562 | CAAAAAA | C | 17 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0002t0002g0008 others(14): Show |
37 | HG01071.hp1 HG01109.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.41+824_41+829delAA others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776562 | CAAAAAAA | C | 19 | a0001c0001t0001g0048 a0001c0001t0049g0082 a0001c0002t0003g0017 others(16): Show |
24 | HG00280.hp2 HG01070.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.41+823_41+829delAA others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776562 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41+817_41+829delAA others(11): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | ||||||
chr7:4776689 | G | A | 1 | a0005c0018t0019g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+933G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776689 | |||||||
chr7:4776697 | T | C | 43 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0002g0053 others(40): Show |
73 | HG00544.hp2 HG00597.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.41+941T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776697 | |||||||
chr7:4776807 | G | A | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+1051G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776807 | |||||||
chr7:4776856 | G | A | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+1100G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776856 | |||||||
chr7:4776870 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.41+1114A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776870 | |||||||
chr7:4776943 | C | T | 18 | a0001c0002t0006g0012 a0001c0002t0006g0089 a0001c0002t0006g0158 others(15): Show |
24 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.41+1187C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776943 | |||||||
chr7:4776989 | G | T | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+1233G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776989 | |||||||
chr7:4776990 | C | T | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+1234C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776990 | |||||||
chr7:4777019 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41+1263G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777019 | |||||||
chr7:4777037 | C | A | 12 | a0001c0001t0001g0102 a0001c0002t0017g0024 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+1281C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777037 | |||||||
chr7:4777125 | C | G | 22 | a0001c0001t0002g0053 a0001c0014t0006g0090 a0002c0003t0002g0004 others(19): Show |
33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+1369C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777125 | |||||||
chr7:4777145 | C | A | 1 | a0012c0019t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.41+1389C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777145 | |||||||
chr7:4777156 | A | T | 1 | a0001c0002t0003g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41+1400A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777156 | |||||||
chr7:4777166 | GAT | G | 19 | a0001c0001t0002g0053 a0002c0003t0002g0004 a0002c0003t0002g0014 others(16): Show |
30 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.41+1413_41+1414del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777166 | ||||||
chr7:4777170 | T | C | 19 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0002t0002g0008 others(16): Show |
39 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.41+1414T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777170 | |||||||
chr7:4777197 | A | G | 8 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(5): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+1441A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777197 | |||||||
chr7:4777353 | C | CTTTA | 53 | a0001c0001t0001g0036 a0001c0001t0001g0105 a0001c0001t0001g0106 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.41+1629_41+1632dup others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | ||||||
chr7:4777353 | C | CTTTATTT others(1): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0002t0003g0009 others(14): Show |
30 | HG01891.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.41+1625_41+1632dup others(8): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | ||||||
chr7:4777353 | C | CTTTATTT others(5): Show |
2 | a0001c0002t0003g0073 a0001c0006t0003g0074 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.41+1621_41+1632dup others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | ||||||
chr7:4777426 | C | T | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.41+1670C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777426 | |||||||
chr7:4777444 | A | G | 1 | a0005c0018t0019g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+1688A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777444 | |||||||
chr7:4777476 | C | T | 2 | a0003c0004t0007g0016 a0003c0004t0007g0072 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+1720C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777476 | |||||||
chr7:4777587 | C | G | 1 | a0019c0029t0020g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.41+1831C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777587 | |||||||
chr7:4777623 | A | G | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+1867A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777623 | |||||||
chr7:4777648 | C | T | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.41+1892C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777648 | |||||||
chr7:4777656 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.41+1900C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777656 | |||||||
chr7:4777744 | C | T | 1 | a0001c0001t0035g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+1988C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777744 | |||||||
chr7:4777756 | T | C | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2000T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777756 | |||||||
chr7:4777822 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.41+2066A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777822 | |||||||
chr7:4777829 | T | C | 11 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(8): Show |
16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+2073T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777829 | |||||||
chr7:4777836 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.41+2080A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777836 | |||||||
chr7:4777932 | C | T | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+2176C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777932 | |||||||
chr7:4777957 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.41+2201G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777957 | |||||||
chr7:4777985 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.41+2229G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777985 | |||||||
chr7:4778039 | C | T | 1 | a0002c0003t0002g0026 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.41+2283C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778039 | |||||||
chr7:4778047 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41+2291G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778047 | |||||||
chr7:4778082 | A | G | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+2326A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778082 | |||||||
chr7:4778193 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.41+2437C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778193 | |||||||
chr7:4778321 | G | T | 11 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(8): Show |
16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+2565G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778321 | |||||||
chr7:4778377 | G | A | 1 | a0012c0019t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.41+2621G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778377 | |||||||
chr7:4778390 | G | A | 1 | a0001c0001t0041g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+2634G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778390 | |||||||
chr7:4778455 | A | T | 61 | a0001c0001t0002g0010 a0001c0001t0002g0053 a0001c0001t0006g0010 others(58): Show |
97 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(94): Show |
intron_variant | MODIFIER | c.41+2699A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778455 | |||||||
chr7:4778509 | T | C | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42-2666T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778509 | |||||||
chr7:4778544 | C | T | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2631C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778544 | |||||||
chr7:4778660 | T | A | 24 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(21): Show |
40 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.42-2515T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778660 | |||||||
chr7:4778665 | G | A | 5 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0032g0077 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2510G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778665 | |||||||
chr7:4778713 | A | G | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2462A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778713 | |||||||
chr7:4778759 | TTA | T | 6 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0002t0003g0009 others(3): Show |
10 | HG01109.hp1 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-2410_42-2409del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778759 | ||||||
chr7:4778766 | T | G | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-2409T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778766 | |||||||
chr7:4778785 | TATATA | T | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-2382_42-2378del others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778785 | ||||||
chr7:4778817 | GTTATA | G | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2351_42-2347del others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778817 | ||||||
chr7:4778829 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.42-2346A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778829 | |||||||
chr7:4778957 | A | G | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.42-2218A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778957 | |||||||
chr7:4779043 | T | G | 2 | a0001c0001t0001g0037 a0001c0002t0036g0051 |
3 | HG00438.hp2 HG02109.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.42-2132T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779043 | |||||||
chr7:4779043 | TATAG | T | 8 | a0001c0001t0001g0110 a0001c0001t0005g0005 a0001c0001t0005g0013 others(5): Show |
15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-2116_42-2113del others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779043 | ||||||
chr7:4779046 | A | T | 1 | a0001c0014t0006g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-2129A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779046 | |||||||
chr7:4779047 | G | T | 21 | a0001c0001t0002g0053 a0002c0003t0002g0004 a0002c0003t0002g0014 others(18): Show |
32 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.42-2128G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779047 | |||||||
chr7:4779057 | T | C | 1 | a0002c0003t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.42-2118T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779057 | |||||||
chr7:4779161 | A | G | 30 | a0001c0001t0002g0053 a0001c0002t0006g0012 a0001c0002t0006g0088 others(27): Show |
43 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.42-2014A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779161 | |||||||
chr7:4779180 | A | G | 1 | a0001c0006t0003g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42-1995A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779180 | |||||||
chr7:4779208 | A | T | 1 | a0001c0014t0006g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-1967A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779208 | |||||||
chr7:4779221 | CAT | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0010c0013t0021g0029 others(2): Show |
7 | HG00738.hp2 HG01071.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-1949_42-1948del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779221 | ||||||
chr7:4779238 | A | G | 24 | a0001c0002t0017g0024 a0001c0002t0027g0080 a0001c0002t0036g0051 others(21): Show |
40 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.42-1937A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779238 | |||||||
chr7:4779316 | CAT | C | 12 | a0001c0001t0005g0005 a0001c0001t0005g0013 a0001c0001t0005g0104 others(9): Show |
20 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1857_42-1856del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779316 | ||||||
chr7:4779319 | A | G | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42-1856A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779319 | |||||||
chr7:4779342 | CAT | C | 4 | a0001c0001t0002g0114 a0001c0002t0006g0089 a0001c0002t0027g0080 others(1): Show |
4 | HG01496.hp2 HG02896.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-1829_42-1828del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779342 | ||||||
chr7:4779344 | T | TAACACGT others(17): Show |
5 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(2): Show |
6 | HG01081.hp1 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-1830_42-1829ins others(24): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779344 | ||||||
chr7:4779374 | A | G | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1801A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779374 | |||||||
chr7:4779376 | G | C | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1799G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779376 | |||||||
chr7:4779377 | T | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1798T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779377 | |||||||
chr7:4779378 | C | CAT | 16 | a0001c0002t0027g0080 a0001c0002t0036g0051 a0001c0005t0009g0030 others(13): Show |
20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1793_42-1792dup others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779378 | ||||||
chr7:4779378 | C | CATATAAC others(18): Show |
3 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0025t0006g0010 |
4 | HG01109.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-1784_42-1760dup others(25): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779378 | ||||||
chr7:4779378 | C | T | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1797C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779378 | |||||||
chr7:4779410 | CATG | C | 7 | a0001c0002t0027g0080 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-1762_42-1760del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779410 | ||||||
chr7:4779430 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.42-1745A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779430 | |||||||
chr7:4779436 | CAT | C | 13 | a0001c0002t0017g0024 a0001c0002t0027g0080 a0001c0005t0009g0030 others(10): Show |
18 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-1733_42-1732del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779436 | ||||||
chr7:4779439 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42-1736A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779439 | |||||||
chr7:4779457 | CAT | C | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-1711_42-1710del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779457 | ||||||
chr7:4779479 | T | C | 12 | a0001c0002t0017g0024 a0001c0002t0027g0080 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-1696T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779479 | |||||||
chr7:4779481 | TA | T | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-1693delA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779481 | |||||||
chr7:4779482 | A | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0125 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-1693A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779482 | |||||||
chr7:4779482 | AT | A | 14 | a0001c0002t0017g0024 a0001c0002t0027g0080 a0001c0005t0009g0030 others(11): Show |
19 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-1684delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779482 | ||||||
chr7:4779484 | T | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0093 a0001c0001t0001g0102 others(64): Show |
110 | HG00099.hp1 HG00597.hp1 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.42-1691T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779484 | |||||||
chr7:4779485 | T | A | 2 | a0002c0003t0011g0057 a0018c0017t0024g0091 |
2 | HG03139.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.42-1690T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779485 | |||||||
chr7:4779641 | T | A | 1 | a0001c0002t0003g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42-1534T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779641 | |||||||
chr7:4779685 | A | C | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-1490A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779685 | |||||||
chr7:4779713 | T | C | 12 | a0001c0002t0017g0024 a0001c0002t0027g0080 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-1462T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779713 | |||||||
chr7:4779757 | C | T | 9 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(6): Show |
13 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-1418C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779757 | |||||||
chr7:4779806 | AT | A | 15 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(12): Show |
20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1360delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779806 | ||||||
chr7:4779884 | C | G | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-1291C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779884 | |||||||
chr7:4779894 | C | T | 6 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(3): Show |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-1281C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779894 | |||||||
chr7:4780005 | A | G | 5 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0032g0077 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-1170A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780005 | |||||||
chr7:4780010 | C | T | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-1165C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780010 | |||||||
chr7:4780083 | G | A | 1 | a0001c0002t0006g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-1092G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780083 | |||||||
chr7:4780093 | C | T | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42-1082C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780093 | |||||||
chr7:4780107 | C | T | 6 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(3): Show |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-1068C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780107 | |||||||
chr7:4780110 | A | T | 2 | a0010c0013t0021g0029 a0010c0013t0045g0029 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.42-1065A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780110 | |||||||
chr7:4780129 | A | G | 11 | a0001c0002t0017g0024 a0001c0005t0009g0030 a0001c0005t0009g0031 others(8): Show |
16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-1046A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780129 | |||||||
chr7:4780236 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.42-939T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780236 | |||||||
chr7:4780285 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.42-890A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780285 | |||||||
chr7:4780358 | G | A | 1 | a0019c0029t0020g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.42-817G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780358 | |||||||
chr7:4780411 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.42-764A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780411 | |||||||
chr7:4780412 | GT | G | 55 | a0001c0001t0001g0116 a0001c0001t0001g0154 a0001c0001t0002g0010 others(52): Show |
80 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.42-759delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4780412 | ||||||
chr7:4780485 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.42-690C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780485 | |||||||
chr7:4780487 | A | G | 9 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
10 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-688A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780487 | |||||||
chr7:4780517 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42-658C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780517 | |||||||
chr7:4780530 | C | G | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-645C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780530 | |||||||
chr7:4780531 | G | C | 5 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(2): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-644G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780531 | |||||||
chr7:4780637 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.42-538G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780637 | |||||||
chr7:4780639 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42-536G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780639 | |||||||
chr7:4780652 | T | G | 68 | a0001c0001t0001g0118 a0001c0001t0002g0010 a0001c0001t0006g0010 others(65): Show |
106 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(103): Show |
intron_variant | MODIFIER | c.42-523T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780652 | |||||||
chr7:4780715 | G | A | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-460G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780715 | |||||||
chr7:4780765 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.42-410C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780765 | |||||||
chr7:4780792 | T | C | 18 | a0001c0002t0017g0024 a0001c0002t0036g0051 a0001c0005t0009g0030 others(15): Show |
23 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-383T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780792 | |||||||
chr7:4780950 | T | C | 23 | a0001c0001t0010g0038 a0001c0001t0030g0038 a0002c0003t0002g0004 others(20): Show |
34 | HG00597.hp1 HG00609.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-225T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780950 | |||||||
chr7:4781002 | CAGCTCAG others(21): Show |
C | 1 | a0001c0001t0001g0119 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.42-170_42-143delCT others(26): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4781002 | ||||||
chr7:4781018 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.42-157C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781018 | |||||||
chr7:4781029 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0140 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42-146C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781029 | |||||||
chr7:4781031 | A | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0140 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42-144A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781031 | |||||||
chr7:4781098 | C | T | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781098 | |||||||
chr7:4781425 | T | G | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+113T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781425 | |||||||
chr7:4781491 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.180-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781491 | |||||||
chr7:4781523 | C | T | 1 | a0001c0001t0001g0044 | 2 | NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.180-45C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781523 | |||||||
chr7:4781540 | C | T | 5 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(2): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.180-28C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781540 | |||||||
chr7:4781924 | G | A | 22 | a0001c0014t0006g0090 a0001c0014t0029g0087 a0002c0003t0002g0004 others(19): Show |
33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.366+170G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781924 | |||||||
chr7:4781966 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.366+212A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781966 | |||||||
chr7:4781996 | C | G | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+242C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781996 | |||||||
chr7:4782013 | G | A | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.366+259G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782013 | |||||||
chr7:4782209 | C | T | 1 | a0001c0001t0026g0138 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.366+455C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782209 | |||||||
chr7:4782340 | C | T | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+586C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782340 | |||||||
chr7:4782426 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.366+672C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782426 | |||||||
chr7:4782473 | G | A | 1 | a0014c0028t0047g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.366+719G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782473 | |||||||
chr7:4782604 | T | G | 1 | a0001c0001t0001g0039 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.367-712T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782604 | |||||||
chr7:4782677 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.367-639C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782677 | |||||||
chr7:4782706 | G | C | 1 | a0001c0001t0001g0039 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.367-610G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782706 | |||||||
chr7:4782769 | TCTC | T | 23 | a0001c0002t0003g0070 a0001c0014t0006g0090 a0001c0014t0029g0087 others(20): Show |
34 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.367-543_367-541del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 4782769 | ||||||
chr7:4782785 | A | G | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-531A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782785 | |||||||
chr7:4782827 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.367-489C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782827 | |||||||
chr7:4782829 | C | T | 8 | a0001c0001t0049g0082 a0001c0002t0044g0079 a0001c0005t0009g0030 others(5): Show |
9 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-487C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782829 | |||||||
chr7:4782834 | G | A | 1 | a0019c0029t0020g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.367-482G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782834 | |||||||
chr7:4782897 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0117 others(1): Show |
6 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-419G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782897 | |||||||
chr7:4782945 | C | T | 12 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(9): Show |
16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.367-371C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782945 | |||||||
chr7:4782955 | T | C | 5 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(2): Show |
6 | HG01081.hp1 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-361T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782955 | |||||||
chr7:4783006 | C | G | 4 | a0001c0002t0002g0008 a0001c0002t0003g0008 a0001c0002t0003g0068 others(1): Show |
7 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-310C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783006 | |||||||
chr7:4783011 | C | T | 3 | a0003c0004t0007g0095 a0005c0011t0007g0027 a0005c0018t0019g0052 |
4 | HG01243.hp2 HG02451.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-305C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783011 | |||||||
chr7:4783022 | G | T | 1 | a0001c0002t0044g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367-294G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783022 | |||||||
chr7:4783035 | G | A | 1 | a0012c0019t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.367-281G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783035 | |||||||
chr7:4783077 | C | T | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.367-239C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783077 | |||||||
chr7:4783096 | C | G | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-220C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783096 | |||||||
chr7:4783147 | G | C | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-169G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783147 | |||||||
chr7:4783256 | T | C | 12 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.367-60T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783256 | |||||||
chr7:4783258 | GGGGAGCT others(13): Show |
G | 2 | a0001c0002t0032g0077 a0001c0002t0033g0069 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-55_367-36delGA others(18): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 4783258 | ||||||
chr7:4783526 | A | G | 2 | a0001c0014t0006g0090 a0001c0014t0029g0087 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.511+66A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783526 | |||||||
chr7:4783547 | G | T | 20 | a0002c0003t0002g0004 a0002c0003t0002g0014 a0002c0003t0002g0026 others(17): Show |
31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.511+87G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783547 | |||||||
chr7:4783555 | G | T | 20 | a0002c0003t0002g0004 a0002c0003t0002g0014 a0002c0003t0002g0026 others(17): Show |
31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.511+95G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783555 | |||||||
chr7:4783564 | G | A | 4 | a0006c0008t0013g0086 a0010c0013t0021g0029 a0010c0013t0045g0029 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+104G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783564 | |||||||
chr7:4783573 | C | T | 1 | a0001c0001t0026g0138 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.511+113C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783573 | |||||||
chr7:4783574 | G | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.511+114G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783574 | |||||||
chr7:4783578 | G | T | 5 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0032g0077 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-111G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783578 | |||||||
chr7:4783643 | C | A | 1 | a0001c0014t0006g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.512-46C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783643 | |||||||
chr7:4783662 | C | G | 1 | a0001c0002t0003g0009 | 4 | HG02559.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-27C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783662 | |||||||
chr7:4783682 | A | G | 24 | a0001c0001t0035g0150 a0001c0002t0002g0008 a0001c0002t0003g0008 others(21): Show |
44 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.512-7A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783682 | |||||||
chr7:4783874 | A | G | 1 | a0001c0001t0026g0138 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.621+76A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783874 | |||||||
chr7:4783929 | G | T | 1 | a0001c0002t0003g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+131G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783929 | |||||||
chr7:4783966 | G | A | 8 | a0001c0001t0005g0005 a0001c0001t0005g0013 a0001c0001t0005g0104 others(5): Show |
15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.621+168G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783966 | |||||||
chr7:4784034 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.622-169C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784034 | |||||||
chr7:4784092 | G | A | 6 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(3): Show |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-111G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784092 | |||||||
chr7:4784099 | T | C | 1 | a0001c0002t0036g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.622-104T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784099 | |||||||
chr7:4784113 | C | T | 1 | a0001c0001t0049g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622-90C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784113 | |||||||
chr7:4784151 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.622-52G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784151 | |||||||
chr7:4784394 | G | A | 1 | a0001c0001t0005g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.790+23G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784394 | |||||||
chr7:4784400 | CAG | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0136 a0001c0002t0036g0051 |
3 | HG02109.hp2 NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.790+30_790+31delAG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784400 | |||||||
chr7:4784453 | G | A | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.790+82G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784453 | |||||||
chr7:4784500 | A | G | 9 | a0001c0001t0049g0082 a0001c0005t0009g0031 a0001c0005t0009g0083 others(6): Show |
13 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.790+129A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784500 | |||||||
chr7:4784680 | C | T | 7 | a0001c0002t0002g0008 a0001c0002t0003g0008 a0001c0002t0003g0068 others(4): Show |
12 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-228C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784680 | |||||||
chr7:4784686 | G | A | 5 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0032g0077 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.791-222G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784686 | |||||||
chr7:4784798 | C | T | 11 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(8): Show |
22 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.791-110C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784798 | |||||||
chr7:4784903 | C | T | 2 | a0001c0002t0003g0070 a0001c0002t0031g0058 |
2 | HG03579.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.791-5C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784903 | |||||||
chr7:4785256 | A | G | 77 | a0001c0001t0049g0082 a0001c0002t0002g0008 a0001c0002t0003g0008 others(74): Show |
119 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.932-159A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785256 | |||||||
chr7:4785312 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.932-103C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785312 | |||||||
chr7:4785372 | T | C | 9 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(6): Show |
12 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-43T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785372 | |||||||
chr7:4785486 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0140 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.969+34C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785486 | |||||||
chr7:4785491 | C | T | 1 | a0001c0001t0049g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.970-31C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785491 | |||||||
chr7:4785492 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.970-30G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785492 | |||||||
chr7:4785509 | C | T | 16 | a0001c0002t0002g0008 a0001c0002t0003g0008 a0001c0002t0003g0009 others(13): Show |
29 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.970-13C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785509 | |||||||
chr7:4785698 | G | T | 2 | a0001c0014t0006g0090 a0001c0014t0029g0087 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1132+14G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785698 | |||||||
chr7:4785713 | C | CG | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132+33dupG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785713 | ||||||
chr7:4785743 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG00621.hp2 HG00642.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1132+59A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785743 | |||||||
chr7:4785760 | C | CT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0132 others(22): Show |
42 | HG00544.hp1 HG01175.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1132+96dupT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | ||||||
chr7:4785760 | C | CTT | 9 | a0001c0002t0003g0070 a0001c0002t0006g0012 a0001c0002t0006g0088 others(6): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1132+95_1132+96dup others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | ||||||
chr7:4785760 | CT | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(13): Show |
20 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1132+96delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | ||||||
chr7:4785760 | CTT | C | 5 | a0006c0008t0013g0032 a0006c0008t0013g0086 a0007c0009t0001g0001 others(2): Show |
6 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132+95_1132+96del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | ||||||
chr7:4785760 | CTTT | C | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132+94_1132+96del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | ||||||
chr7:4785762 | T | G | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1132+78T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785762 | |||||||
chr7:4785788 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1132+104T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785788 | |||||||
chr7:4785883 | G | T | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1132+199G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785883 | |||||||
chr7:4785943 | G | A | 6 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0027g0080 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132+259G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785943 | |||||||
chr7:4785966 | G | C | 2 | a0011c0010t0023g0033 a0011c0010t0025g0033 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1132+282G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785966 | |||||||
chr7:4785984 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1133-266T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785984 | |||||||
chr7:4785995 | C | T | 7 | a0001c0002t0002g0008 a0001c0002t0003g0008 a0001c0002t0003g0068 others(4): Show |
12 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1133-255C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785995 | |||||||
chr7:4786011 | C | T | 3 | a0001c0006t0003g0011 a0001c0006t0003g0074 a0001c0006t0003g0075 |
6 | HG02717.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1133-239C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786011 | |||||||
chr7:4786055 | G | T | 48 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(45): Show |
75 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.1133-195G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786055 | |||||||
chr7:4786125 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1133-125G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786125 | |||||||
chr7:4786220 | C | T | 12 | a0002c0003t0002g0004 a0002c0003t0002g0014 a0002c0003t0002g0055 others(9): Show |
22 | HG00597.hp1 HG02074.hp2 HG02698.hp1 others(19): Show |
intron_variant | MODIFIER | c.1133-30C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786220 | |||||||
chr7:4786469 | T | TA | 22 | a0001c0002t0002g0008 a0001c0002t0003g0008 a0001c0002t0003g0009 others(19): Show |
37 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1311+43dupA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 4786469 | ||||||
chr7:4786500 | C | T | 1 | a0003c0004t0004g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1311+72C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786500 | |||||||
chr7:4786518 | C | G | 1 | a0002c0003t0002g0064 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1311+90C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786518 | |||||||
chr7:4786547 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0119 |
3 | HG00544.hp1 NA18944.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1311+119G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786547 | |||||||
chr7:4786557 | T | C | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+129T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786557 | |||||||
chr7:4786560 | G | A | 9 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(6): Show |
12 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1311+132G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786560 | |||||||
chr7:4786575 | G | A | 2 | a0002c0003t0002g0014 a0002c0030t0002g0014 |
3 | NA18969.hp2 NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1311+147G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786575 | |||||||
chr7:4786592 | C | G | 1 | a0019c0029t0020g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1311+164C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786592 | |||||||
chr7:4786615 | G | A | 1 | a0001c0001t0016g0023 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1311+187G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786615 | |||||||
chr7:4786667 | A | G | 1 | a0001c0001t0010g0019 | 3 | HG00280.hp1 HG01168.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1311+239A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786667 | |||||||
chr7:4786672 | G | C | 2 | a0001c0014t0006g0090 a0001c0014t0029g0087 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1311+244G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786672 | |||||||
chr7:4786708 | T | C | 46 | a0001c0001t0049g0082 a0001c0002t0036g0051 a0001c0005t0009g0030 others(43): Show |
72 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.1311+280T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786708 | |||||||
chr7:4786885 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+457G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786885 | |||||||
chr7:4786951 | T | C | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311+523T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786951 | |||||||
chr7:4786969 | G | A | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+541G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786969 | |||||||
chr7:4787000 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1311+572G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787000 | |||||||
chr7:4787010 | G | T | 1 | a0001c0001t0049g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1311+582G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787010 | |||||||
chr7:4787018 | T | C | 24 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(21): Show |
39 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1311+590T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787018 | |||||||
chr7:4787062 | G | T | 1 | a0009c0012t0046g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312-572G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787062 | |||||||
chr7:4787063 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1312-571C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787063 | |||||||
chr7:4787108 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0025t0006g0010 |
4 | HG01109.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-526C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787108 | |||||||
chr7:4787113 | C | T | 1 | a0001c0002t0003g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312-521C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787113 | |||||||
chr7:4787114 | G | A | 1 | a0001c0001t0001g0007 | 6 | HG02132.hp2 NA18952.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-520G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787114 | |||||||
chr7:4787198 | G | A | 2 | a0005c0011t0007g0027 a0009c0012t0046g0161 |
3 | HG01243.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1312-436G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787198 | |||||||
chr7:4787228 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1312-406C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787228 | |||||||
chr7:4787248 | C | T | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1312-386C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787248 | |||||||
chr7:4787253 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1312-381G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787253 | |||||||
chr7:4787315 | A | C | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-319A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787315 | |||||||
chr7:4787336 | A | C | 16 | a0001c0002t0015g0049 a0001c0002t0015g0078 a0001c0002t0032g0077 others(13): Show |
27 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1312-298A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787336 | |||||||
chr7:4787347 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0034g0156 |
2 | NA18960.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1312-287A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787347 | |||||||
chr7:4787429 | T | G | 17 | a0001c0002t0017g0024 a0003c0004t0004g0003 a0003c0004t0004g0054 others(14): Show |
30 | HG01175.hp1 HG01243.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.1312-205T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787429 | |||||||
chr7:4787450 | C | T | 1 | a0001c0001t0008g0042 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1312-184C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787450 | |||||||
chr7:4787457 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1312-177G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787457 | |||||||
chr7:4787465 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0005g0013 a0001c0001t0005g0108 others(6): Show |
11 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312-169G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787465 | |||||||
chr7:4787529 | G | C | 15 | a0001c0002t0017g0024 a0003c0004t0004g0003 a0003c0004t0004g0054 others(12): Show |
27 | HG01175.hp1 HG01243.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.1312-105G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787529 | |||||||
chr7:4787542 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1312-92C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787542 | |||||||
chr7:4787574 | C | T | 3 | a0001c0002t0003g0071 a0003c0004t0007g0016 a0003c0004t0007g0072 |
5 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-60C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787574 | |||||||
chr7:4787614 | C | T | 4 | a0001c0014t0006g0090 a0001c0014t0029g0087 a0006c0008t0013g0032 others(1): Show |
5 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-20C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787614 | |||||||
chr7:4787849 | T | C | 31 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(28): Show |
46 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1454+73T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4787849 | |||||||
chr7:4787867 | C | T | 2 | a0001c0014t0006g0090 a0001c0014t0029g0087 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1454+91C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4787867 | |||||||
chr7:4788006 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0139 a0001c0001t0001g0159 others(1): Show |
4 | HG00741.hp1 HG01070.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-148G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788006 | |||||||
chr7:4788015 | T | G | 3 | a0001c0002t0003g0071 a0003c0004t0007g0016 a0003c0004t0007g0072 |
5 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455-139T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788015 | |||||||
chr7:4788065 | A | C | 11 | a0001c0002t0003g0017 a0001c0002t0003g0073 a0001c0002t0003g0081 others(8): Show |
18 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1455-89A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788065 | |||||||
chr7:4788077 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1455-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788077 | |||||||
chr7:4788117 | C | T | 4 | a0001c0021t0001g0131 a0010c0013t0021g0029 a0010c0013t0045g0029 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-37C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788117 | |||||||
chr7:4788118 | G | A | 1 | a0004c0007t0012g0015 | 3 | HG01074.hp2 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1455-36G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788118 | |||||||
chr7:4788323 | C | A | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+29C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788323 | |||||||
chr7:4788341 | G | A | 19 | a0002c0003t0002g0004 a0002c0003t0002g0014 a0002c0003t0002g0026 others(16): Show |
30 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1595+47G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788341 | |||||||
chr7:4788365 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1595+71C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788365 | |||||||
chr7:4788397 | T | G | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1595+103T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788397 | |||||||
chr7:4788446 | C | T | 32 | a0001c0002t0017g0024 a0002c0003t0002g0004 a0002c0003t0002g0014 others(29): Show |
55 | HG00597.hp1 HG01074.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.1595+152C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788446 | |||||||
chr7:4788470 | G | A | 2 | a0011c0010t0023g0033 a0011c0010t0025g0033 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1595+176G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788470 | |||||||
chr7:4788505 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1595+211C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788505 | |||||||
chr7:4788528 | A | G | 26 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(23): Show |
42 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1595+234A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788528 | |||||||
chr7:4788532 | T | C | 42 | a0001c0001t0002g0114 a0001c0001t0049g0082 a0001c0002t0002g0008 others(39): Show |
73 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.1595+238T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788532 | |||||||
chr7:4788535 | C | T | 17 | a0001c0001t0002g0114 a0001c0002t0002g0008 a0001c0002t0003g0008 others(14): Show |
30 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1595+241C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788535 | |||||||
chr7:4788598 | G | A | 1 | a0009c0012t0046g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1596-242G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788598 | |||||||
chr7:4788641 | T | C | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596-199T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788641 | |||||||
chr7:4788763 | G | A | 1 | a0001c0014t0029g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1596-77G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788763 | |||||||
chr7:4788765 | A | G | 1 | a0003c0004t0004g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1596-75A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788765 | |||||||
chr7:4788774 | G | A | 27 | a0001c0002t0006g0012 a0001c0002t0006g0088 a0001c0002t0006g0089 others(24): Show |
40 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.1596-66G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788774 | |||||||
chr7:4788780 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1596-60C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788780 | |||||||
chr7:4788781 | C | T | 2 | a0001c0014t0006g0090 a0001c0014t0029g0087 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1596-59C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788781 | |||||||
chr7:4788808 | G | A | 2 | a0011c0010t0023g0033 a0011c0010t0025g0033 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596-32G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788808 | |||||||
chr7:4788959 | C | T | 1 | a0008c0034t0001g0126 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.1707+8C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788959 | |||||||
chr7:4788962 | T | C | 50 | a0001c0001t0002g0010 a0001c0001t0006g0010 a0001c0002t0006g0012 others(47): Show |
79 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1707+11T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788962 | |||||||
chr7:4788997 | T | C | 55 | a0001c0001t0049g0082 a0001c0002t0006g0012 a0001c0002t0006g0088 others(52): Show |
84 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.1707+46T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788997 | |||||||
chr7:4789076 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1707+125G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789076 | |||||||
chr7:4789097 | G | C | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1707+146G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789097 | |||||||
chr7:4789125 | G | A | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1707+174G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789125 | |||||||
chr7:4789161 | G | A | 7 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(4): Show |
18 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1707+210G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789161 | |||||||
chr7:4789169 | GTCCCCGT others(36): Show |
G | 1 | a0004c0007t0012g0015 | 3 | HG01074.hp2 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1707+249_1707+291d others(45): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 4789169 | ||||||
chr7:4789183 | C | T | 2 | a0001c0002t0015g0049 a0001c0002t0044g0079 |
2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1707+232C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789183 | |||||||
chr7:4789188 | C | T | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+237C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789188 | |||||||
chr7:4789189 | A | G | 4 | a0001c0002t0015g0049 a0001c0002t0032g0077 a0001c0002t0033g0069 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+238A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789189 | |||||||
chr7:4789191 | C | T | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+240C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789191 | |||||||
chr7:4789194 | G | A | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+243G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789194 | |||||||
chr7:4789202 | A | C | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+251A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789202 | |||||||
chr7:4789206 | C | T | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+255C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789206 | |||||||
chr7:4789212 | A | G | 1 | a0004c0007t0012g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+261A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789212 | |||||||
chr7:4789265 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1707+314C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789265 | |||||||
chr7:4789297 | C | G | 14 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(11): Show |
25 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+346C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789297 | |||||||
chr7:4789320 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1707+369A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789320 | |||||||
chr7:4789350 | G | T | 10 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(7): Show |
13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1707+399G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789350 | |||||||
chr7:4789369 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1707+418C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789369 | |||||||
chr7:4789396 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1708-436C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789396 | |||||||
chr7:4789432 | G | GCCCCCCA others(18): Show |
1 | a0001c0001t0001g0145 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1708-396_1708-372d others(27): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 4789432 | ||||||
chr7:4789488 | A | G | 8 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(5): Show |
19 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1708-344A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789488 | |||||||
chr7:4789541 | C | T | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1708-291C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789541 | |||||||
chr7:4789545 | C | G | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1708-287C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789545 | |||||||
chr7:4789582 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1708-250G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789582 | |||||||
chr7:4789585 | A | C | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1708-247A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789585 | |||||||
chr7:4789661 | G | A | 10 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(7): Show |
13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1708-171G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789661 | |||||||
chr7:4789730 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0050 others(11): Show |
28 | HG00438.hp2 HG02129.hp2 NA18747.hp1 others(25): Show |
intron_variant | MODIFIER | c.1708-102C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789730 | |||||||
chr7:4789733 | C | T | 3 | a0011c0010t0023g0033 a0011c0010t0025g0033 a0018c0017t0024g0091 |
3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1708-99C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789733 | |||||||
chr7:4789740 | C | G | 26 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(23): Show |
42 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1708-92C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789740 | |||||||
chr7:4789818 | C | T | 3 | a0002c0003t0002g0026 a0002c0003t0002g0062 a0002c0003t0002g0063 |
4 | HG03491.hp2 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708-14C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789818 | |||||||
chr7:4789827 | C | T | 1 | a0002c0003t0002g0063 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.1708-5C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789827 | |||||||
chr7:4789969 | T | G | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1805+40T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4789969 | |||||||
chr7:4789981 | TCCTCCCC others(6): Show |
T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1805+61_1805+73del others(13): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789981 | ||||||
chr7:4789984 | TCCCCCTC others(7): Show |
T | 1 | a0005c0018t0019g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1805+63_1805+76del others(14): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789984 | ||||||
chr7:4789985 | CCCCCTCT | C | 4 | a0003c0004t0007g0095 a0010c0013t0021g0029 a0010c0013t0045g0029 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1805+63_1805+69del others(7): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789985 | ||||||
chr7:4789990 | TCTCCCCT others(5): Show |
T | 10 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(7): Show |
13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1805+69_1805+80del others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789990 | ||||||
chr7:4789992 | T | C | 9 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(6): Show |
20 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1805+63T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4789992 | |||||||
chr7:4790002 | C | G | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1805+73C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790002 | |||||||
chr7:4790044 | C | A | 3 | a0010c0013t0021g0029 a0010c0013t0045g0029 a0019c0029t0020g0076 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1805+115C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790044 | |||||||
chr7:4790054 | A | C | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1805+125A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790054 | |||||||
chr7:4790070 | ACCCACAG others(1): Show |
A | 18 | a0001c0001t0002g0114 a0001c0002t0002g0008 a0001c0002t0003g0008 others(15): Show |
31 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1805+148_1805+155d others(10): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790070 | ||||||
chr7:4790077 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1805+148G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790077 | |||||||
chr7:4790100 | TTCTC | T | 11 | a0003c0004t0004g0003 a0003c0004t0004g0054 a0003c0004t0004g0066 others(8): Show |
22 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1805+175_1805+178d others(6): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790100 | ||||||
chr7:4790110 | T | C | 53 | a0001c0001t0049g0082 a0001c0002t0006g0012 a0001c0002t0006g0088 others(50): Show |
82 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1805+181T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790110 | |||||||
chr7:4790126 | C | CCT | 60 | a0001c0001t0049g0082 a0001c0002t0006g0012 a0001c0002t0006g0088 others(57): Show |
89 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(86): Show |
intron_variant | MODIFIER | c.1805+197_1805+198i others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790126 | |||||||
chr7:4790132 | T | C | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1805+203T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790132 | |||||||
chr7:4790141 | C | T | 2 | a0001c0002t0018g0028 a0001c0002t0031g0058 |
3 | HG02896.hp2 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1805+212C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790141 | |||||||
chr7:4790150 | C | CCTCTTCA others(7): Show |
1 | a0001c0014t0006g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1805+225_1805+238d others(16): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790150 | ||||||
chr7:4790185 | C | T | 1 | a0018c0017t0024g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1805+256C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790185 | |||||||
chr7:4790198 | G | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0149 |
4 | HG01433.hp2 HG01952.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806-261G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790198 | |||||||
chr7:4790252 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1806-207C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790252 | |||||||
chr7:4790292 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0020c0016t0001g0128 |
3 | HG02602.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1806-167G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790292 | |||||||
chr7:4790307 | C | G | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1806-152C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790307 | |||||||
chr7:4790324 | C | T | 12 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1806-135C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790324 | |||||||
chr7:4790338 | C | T | 6 | a0001c0005t0009g0030 a0001c0005t0009g0031 a0001c0005t0009g0083 others(3): Show |
7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806-121C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790338 | |||||||
chr7:4790354 | C | CACCTACC others(3): Show |
2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806-104_1806-95du others(11): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790354 | ||||||
chr7:4790417 | T | G | 12 | a0001c0001t0049g0082 a0001c0002t0017g0024 a0001c0005t0009g0030 others(9): Show |
17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1806-42T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790417 | |||||||
chr7:4790424 | G | A | 1 | a0001c0002t0006g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1806-35G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790424 | |||||||
chr7:4790447 | C | T | 7 | a0001c0001t0049g0082 a0001c0005t0009g0030 a0001c0005t0009g0031 others(4): Show |
8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1806-12C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790447 | |||||||
chr7:4790602 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1938+11C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 15/16 | chr7 | 4790602 | |||||||
chr7:4790664 | C | T | 11 | a0001c0002t0003g0009 a0001c0002t0003g0017 a0001c0002t0003g0070 others(8): Show |
20 | HG01891.hp2 HG02559.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.1939-9C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 15/16 | chr7 | 4790664 | |||||||
chr7:4790932 | G | C | 1 | a0001c0005t0009g0083 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2153+45G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4790932 | |||||||
chr7:4791032 | C | T | 1 | a0001c0002t0018g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2154-83C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791032 | |||||||
chr7:4791045 | G | C | 2 | a0006c0008t0013g0032 a0006c0008t0013g0086 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2154-70G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791045 | |||||||
chr7:4791047 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2154-68C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791047 | |||||||
chr7:4791063 | C | T | 2 | a0004c0007t0012g0015 a0004c0007t0012g0065 |
4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-52C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791063 | |||||||
chr7:4791074 | G | GGGGAGCA others(15): Show |
1 | a0001c0005t0009g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2154-36_2154-15dup others(22): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 4791074 |