Item | Value |
---|---|
geneid | 161829 |
ensemblid | ENSG00000178997.12 |
hgncid | 28507 |
symbol | EXD1 |
name | exonuclease 3'-5' domain containing 1 |
refseq_nuc | NM_001286441.2 |
refseq_prot | NP_001273370.1 |
ensembl_nuc | ENST00000458580.7 |
ensembl_prot | ENSP00000415056.2 |
mane_status | MANE Select |
chr | chr15 |
start | 41182728 |
end | 41230757 |
strand | - |
ver | v1.2 |
region | chr15:41182728-41230757 |
region5000 | chr15:41177728-41235757 |
regionname0 | EXD1_chr15_41182728_41230757 |
regionname5000 | EXD1_chr15_41177728_41235757 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 572 | 267 | 77 | 47 | 109 | 6 | 27 | 77 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0002 | 1/0 | 572 | 42 | 16 | 11 | 3 | 4 | 7 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0003 | 0/0 | 572 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0004 | 0/0 | 572 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0005 | 0/0 | 572 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0006 | 0/0 | 572 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0007 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0008 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
a0009 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | MDPSS others(567): Show |
chr15 | 41177728 | 41235757 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1716 | 133 | 51 | 14 | 51 | 3 | 14 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0001c0002 | 0/1 | 1716 | 122 | 19 | 32 | 56 | 1 | 13 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0001c0005 | 0/0 | 1716 | 6 | 6 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0001c0006 | 0/0 | 1716 | 3 | 0 | 1 | 0 | 2 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0001c0008 | 0/0 | 1716 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0001c0011 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0002c0003 | 0/0 | 1716 | 32 | 9 | 9 | 3 | 4 | 7 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0002c0004 | 0/0 | 1716 | 8 | 6 | 2 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0002c0013 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0002c0015 | 1/0 | 1716 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0003c0007 | 0/0 | 1716 | 3 | 0 | 0 | 3 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0004c0014 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0005c0009 | 0/0 | 1716 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0006c0017 | 0/0 | 1716 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0007c0010 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0008c0016 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 | ||
a0009c0012 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | ATGGA others(1711): Show |
chr15 | 41177728 | 41235757 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3254 | 11 | 11 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0001t0002 | 0/0 | 3255 | 62 | 17 | 10 | 21 | 2 | 12 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3250): Show |
chr15 | 41177728 | 41235757 |
a0001c0001t0003 | 0/0 | 3254 | 36 | 1 | 4 | 29 | 1 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0001t0004 | 0/0 | 3254 | 22 | 21 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0001t0007 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0001t0015 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0001 | 0/0 | 3254 | 112 | 15 | 31 | 53 | 1 | 12 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0002 | 0/0 | 3255 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3250): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0006 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0008 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0009 | 0/0 | 3254 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0011 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0012 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0013 | 0/1 | 3254 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0002t0014 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0005t0001 | 0/0 | 3254 | 6 | 6 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0006t0001 | 0/0 | 3254 | 3 | 0 | 1 | 0 | 2 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0008t0001 | 0/0 | 3254 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0001c0011t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0003t0001 | 0/0 | 3254 | 27 | 4 | 9 | 3 | 4 | 7 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0003t0005 | 0/0 | 3254 | 4 | 4 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0003t0010 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0004t0001 | 0/0 | 3254 | 8 | 6 | 2 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0013t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0002c0015t0007 | 1/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0003c0007t0003 | 0/0 | 3254 | 3 | 0 | 0 | 3 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0004c0014t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0005c0009t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0006c0017t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0007c0010t0002 | 0/0 | 3255 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3250): Show |
chr15 | 41177728 | 41235757 |
a0008c0016t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
a0009c0012t0003 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | AGACG others(3249): Show |
chr15 | 41177728 | 41235757 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0012g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0013g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0008t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0008t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0010g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0013t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0015t0007g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0004c0014t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0005c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0006c0017t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0007c0010t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0008c0016t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0009c0012t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | GBR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0115 | EUR | GBR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0299 | EUR | FIN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00323 | hp2 | a0001 | c0006 | t0001 | g0266 | EUR | FIN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00642 | hp1 | a0002 | c0003 | t0001 | g0106 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0122 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0127 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0125 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01109 | hp1 | a0002 | c0004 | t0001 | g0006 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01255 | hp1 | a0001 | c0002 | t0009 | g0211 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0121 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01433 | hp2 | a0001 | c0006 | t0001 | g0230 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01515 | hp1 | a0002 | c0003 | t0001 | g0093 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01517 | hp1 | a0001 | c0006 | t0001 | g0249 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0278 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0311 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0118 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02055 | hp1 | a0002 | c0003 | t0005 | g0100 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02145 | hp2 | a0002 | c0004 | t0001 | g0083 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02258 | hp1 | a0002 | c0003 | t0005 | g0099 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0126 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02451 | hp2 | a0001 | c0002 | t0011 | g0265 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0104 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0107 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0316 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0105 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0285 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02809 | hp1 | a0002 | c0003 | t0010 | g0109 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02922 | hp1 | a0002 | c0004 | t0001 | g0129 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0095 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02976 | hp1 | a0001 | c0002 | t0014 | g0094 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0111 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03130 | hp2 | a0002 | c0003 | t0005 | g0101 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03225 | hp1 | a0001 | c0005 | t0001 | g0097 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03453 | hp1 | a0002 | c0004 | t0001 | g0086 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0098 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0117 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0120 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03516 | hp1 | a0002 | c0013 | t0001 | g0032 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03540 | hp2 | a0004 | c0014 | t0001 | g0194 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0294 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0313 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0092 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0123 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0284 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0110 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0091 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04228 | hp1 | a0005 | c0009 | t0001 | g0195 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04228 | hp2 | a0006 | c0017 | t0001 | g0108 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0084 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18944 | hp2 | a0001 | c0008 | t0001 | g0300 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18956 | hp2 | a0001 | c0008 | t0001 | g0301 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18968 | hp1 | a0003 | c0007 | t0003 | g0078 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18971 | hp1 | a0003 | c0007 | t0003 | g0080 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18989 | hp2 | a0007 | c0010 | t0002 | g0090 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19005 | hp2 | a0001 | c0002 | t0008 | g0287 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19010 | hp1 | a0008 | c0016 | t0001 | g0243 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19011 | hp1 | a0009 | c0012 | t0003 | g0132 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19055 | hp1 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19083 | hp2 | a0003 | c0007 | t0003 | g0079 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19240 | hp2 | a0001 | c0002 | t0006 | g0004 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20129 | hp1 | a0002 | c0004 | t0001 | g0001 | AFR | ASW | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ASW | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | TSI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0124 | EUR | TSI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20905 | hp1 | a0001 | c0002 | t0012 | g0238 | SAS | GIH | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | GIH | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0119 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02109 | hp1 | a0001 | c0002 | t0006 | g0003 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02486 | hp1 | a0002 | c0004 | t0001 | g0085 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02559 | hp2 | a0001 | c0011 | t0001 | g0071 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03471 | hp2 | a0001 | c0005 | t0001 | g0096 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
homoSapiens | chm13v2 | a0001 | c0002 | t0013 | g0259 | REF | REF | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
homoSapiens | grch38p0 | a0002 | c0015 | t0007 | g0267 | REF | REF | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184011 | T | C | 7 | a0001 a0003 a0004 others(4): Show |
274 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(271): Show |
missense_variant | MODERATE | c.1639A>G | p.Thr547Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1971/3254 | 1639/1719 | 547/572 | chr15 | 41184011 | |||
chr15:41184130 | T | C | 1 | a0008 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.1520A>G | p.Gln507Arg | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1852/3254 | 1520/1719 | 507/572 | chr15 | 41184130 | |||
chr15:41184224 | C | G | 1 | a0009 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1426G>C | p.Gly476Arg | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1758/3254 | 1426/1719 | 476/572 | chr15 | 41184224 | |||
chr15:41184274 | C | G | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1376G>C | p.Gly459Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1708/3254 | 1376/1719 | 459/572 | chr15 | 41184274 | |||
chr15:41184535 | C | T | 1 | a0007 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1115G>A | p.Arg372His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1447/3254 | 1115/1719 | 372/572 | chr15 | 41184535 | |||
chr15:41191561 | T | C | 1 | a0006 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.745A>G | p.Met249Val | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1077/3254 | 745/1719 | 249/572 | chr15 | 41191561 | |||
chr15:41195839 | C | T | 1 | a0005 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.656G>A | p.Arg219His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/12 | 988/3254 | 656/1719 | 219/572 | chr15 | 41195839 | |||
chr15:41215804 | T | G | 1 | a0003 | 3 | NA18968.hp1 NA18971.hp1 NA19083.hp2 |
missense_variant | MODERATE | c.418A>C | p.Asn140His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/12 | 750/3254 | 418/1719 | 140/572 | chr15 | 41215804 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184267 | G | A | 9 | a0001c0001 a0001c0005 a0002c0003 others(6): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1715/3254 | 1383/1719 | 461/572 | chr15 | 41184267 | |||
chr15:41190033 | T | C | 1 | a0001c0006 | 3 | HG00323.hp2 HG01433.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.960A>G | p.Ala320Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/12 | 1292/3254 | 960/1719 | 320/572 | chr15 | 41190033 | |||
chr15:41191442 | C | T | 1 | a0002c0004 | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.864G>A | p.Gln288Gln | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1196/3254 | 864/1719 | 288/572 | chr15 | 41191442 | |||
chr15:41191484 | A | G | 6 | a0001c0001 a0001c0011 a0002c0013 others(3): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
synonymous_variant | LOW | c.822T>C | p.Pro274Pro | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1154/3254 | 822/1719 | 274/572 | chr15 | 41191484 | |||
chr15:41226495 | G | A | 1 | a0001c0008 | 2 | NA18944.hp2 NA18956.hp2 |
synonymous_variant | LOW | c.81C>T | p.Phe27Phe | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/12 | 413/3254 | 81/1719 | 27/572 | chr15 | 41226495 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41183051 | C | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*880G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 880 | chr15 | 41183051 | ||||||
chr15:41183158 | C | T | 3 | a0001c0001t0003 a0003c0007t0003 a0009c0012t0003 |
40 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*773G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 773 | chr15 | 41183158 | ||||||
chr15:41183167 | G | A | 1 | a0001c0002t0009 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 764 | chr15 | 41183167 | ||||||
chr15:41183273 | G | C | 4 | a0001c0001t0003 a0001c0001t0004 a0003c0007t0003 others(1): Show |
62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*658C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 658 | chr15 | 41183273 | ||||||
chr15:41183332 | T | G | 1 | a0002c0003t0010 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 599 | chr15 | 41183332 | ||||||
chr15:41183460 | T | TA | 3 | a0001c0001t0002 a0001c0002t0002 a0007c0010t0002 |
65 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*470dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 470 | chr15 | 41183460 | ||||||
chr15:41183521 | T | C | 1 | a0001c0002t0011 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 410 | chr15 | 41183521 | ||||||
chr15:41183635 | A | T | 1 | a0001c0002t0008 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 296 | chr15 | 41183635 | ||||||
chr15:41183758 | T | G | 1 | a0002c0003t0005 | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*173A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 173 | chr15 | 41183758 | ||||||
chr15:41183819 | T | C | 1 | a0001c0002t0012 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 112 | chr15 | 41183819 | ||||||
chr15:41226581 | T | C | 1 | a0001c0002t0014 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/12 | 6 | chr15 | 41226581 | ||||||
chr15:41230653 | C | A | 1 | a0001c0001t0015 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/12 | 4078 | chr15 | 41230653 | ||||||
chr15:41230741 | A | T | 1 | a0001c0002t0006 | 2 | HG02109.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-316T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/12 | 4166 | chr15 | 41230741 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184658 | C | CT | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1057-66dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184658 | |||||||
chr15:41184658 | C | CTT | 129 | a0001c0001t0002g0183 a0001c0001t0003g0031 a0001c0002t0001g0041 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1057-67_1057-66dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184658 | |||||||
chr15:41184677 | T | C | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1057-84A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184677 | |||||||
chr15:41184678 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0166 a0001c0001t0002g0181 |
3 | HG01884.hp1 HG02055.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1057-85C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184678 | |||||||
chr15:41184718 | G | A | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1057-125C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184718 | |||||||
chr15:41184816 | A | G | 273 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(270): Show |
274 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.1057-223T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184816 | |||||||
chr15:41184846 | C | T | 1 | a0001c0002t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1057-253G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184846 | |||||||
chr15:41184889 | C | G | 1 | a0001c0001t0002g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1057-296G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184889 | |||||||
chr15:41184935 | C | T | 129 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1057-342G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184935 | |||||||
chr15:41184945 | A | C | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1057-352T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184945 | |||||||
chr15:41184952 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1057-359C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184952 | |||||||
chr15:41185009 | A | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0181 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1057-416T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185009 | |||||||
chr15:41185095 | C | A | 1 | a0001c0001t0004g0012 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1057-502G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185095 | |||||||
chr15:41185107 | G | T | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1057-514C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185107 | |||||||
chr15:41185143 | T | C | 2 | a0002c0003t0001g0116 a0002c0003t0001g0121 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1057-550A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185143 | |||||||
chr15:41185263 | A | AT | 305 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.1057-671dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185263 | |||||||
chr15:41185336 | T | TTTTTG | 60 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(57): Show |
61 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1057-748_1057-744d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185336 | |||||||
chr15:41185357 | A | T | 305 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.1057-764T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185357 | |||||||
chr15:41185361 | T | G | 1 | a0001c0001t0003g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1057-768A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185361 | |||||||
chr15:41185570 | G | C | 1 | a0001c0001t0003g0037 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1057-977C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185570 | |||||||
chr15:41185615 | G | A | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1022C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185615 | |||||||
chr15:41185616 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1023G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185616 | |||||||
chr15:41185628 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1057-1035C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185628 | |||||||
chr15:41185845 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0167 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1057-1252C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185845 | |||||||
chr15:41186150 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1057-1557C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186150 | |||||||
chr15:41186240 | G | A | 138 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
139 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1057-1647C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186240 | |||||||
chr15:41186403 | T | C | 267 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(264): Show |
268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1057-1810A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186403 | |||||||
chr15:41186470 | C | CA | 70 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(67): Show |
71 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.1057-1878dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAA | 11 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0165 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1057-1879_1057-187 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(4): Show |
6 | a0001c0002t0001g0206 a0001c0002t0001g0270 a0001c0002t0001g0271 others(3): Show |
6 | HG01891.hp2 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-1888_1057-187 others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(5): Show |
79 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0191 others(76): Show |
79 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1057-1889_1057-187 others(16): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(6): Show |
40 | a0001c0002t0001g0113 a0001c0002t0001g0114 a0001c0002t0001g0128 others(37): Show |
40 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1057-1890_1057-187 others(17): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(7): Show |
3 | a0001c0002t0001g0239 a0001c0002t0001g0261 a0001c0002t0008g0287 |
3 | HG01109.hp2 HG02148.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1057-1891_1057-187 others(18): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0212 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1057-1892_1057-187 others(19): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186470 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1057-1894_1057-187 others(21): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | |||||||
chr15:41186511 | G | T | 5 | a0001c0005t0001g0007 a0001c0005t0001g0008 a0001c0005t0001g0095 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-1918C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186511 | |||||||
chr15:41186878 | G | A | 2 | a0001c0001t0003g0040 a0001c0001t0003g0061 |
2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1057-2285C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186878 | |||||||
chr15:41186889 | T | C | 6 | a0001c0001t0002g0138 a0001c0001t0002g0144 a0001c0001t0002g0145 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-2296A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186889 | |||||||
chr15:41186890 | TTTTC | T | 6 | a0001c0001t0002g0138 a0001c0001t0002g0144 a0001c0001t0002g0145 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-2301_1057-229 others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186890 | |||||||
chr15:41186894 | C | CT | 51 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0131 others(48): Show |
51 | HG00408.hp1 HG01167.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.1057-2302dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186894 | |||||||
chr15:41186894 | C | T | 1 | a0001c0001t0007g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1057-2301G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186894 | |||||||
chr15:41186988 | G | A | 5 | a0001c0005t0001g0007 a0001c0005t0001g0008 a0001c0005t0001g0095 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-2395C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186988 | |||||||
chr15:41187020 | C | G | 184 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1057-2427G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187020 | |||||||
chr15:41187027 | G | A | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-2434C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187027 | |||||||
chr15:41187385 | C | T | 1 | a0001c0002t0008g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1056+2552G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187385 | |||||||
chr15:41187782 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1056+2155C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187782 | |||||||
chr15:41187857 | A | C | 1 | a0001c0002t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1056+2080T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187857 | |||||||
chr15:41187965 | G | C | 5 | a0001c0005t0001g0007 a0001c0005t0001g0008 a0001c0005t0001g0095 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+1972C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187965 | |||||||
chr15:41187971 | C | T | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1056+1966G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187971 | |||||||
chr15:41188010 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0167 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1056+1927G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188010 | |||||||
chr15:41188013 | C | T | 265 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
266 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1056+1924G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188013 | |||||||
chr15:41188015 | CA | C | 21 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0133 others(18): Show |
21 | HG01175.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+1921delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | |||||||
chr15:41188015 | CAA | C | 170 | a0001c0001t0002g0002 a0001c0001t0002g0131 a0001c0001t0002g0134 others(167): Show |
171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1056+1920_1056+192 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | |||||||
chr15:41188015 | CAAA | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
23 | HG01515.hp1 HG01943.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1056+1919_1056+192 others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | |||||||
chr15:41188015 | CAAAA | C | 92 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1056+1918_1056+192 others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | |||||||
chr15:41188079 | G | T | 3 | a0001c0002t0011g0265 a0001c0002t0014g0094 a0004c0014t0001g0194 |
3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1056+1858C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188079 | |||||||
chr15:41188217 | C | T | 1 | a0004c0014t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1720G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188217 | |||||||
chr15:41188265 | C | T | 2 | a0002c0004t0001g0085 a0002c0004t0001g0086 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1056+1672G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188265 | |||||||
chr15:41188342 | C | G | 1 | a0002c0003t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1056+1595G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188342 | |||||||
chr15:41188350 | C | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+1587G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188350 | |||||||
chr15:41188462 | G | A | 7 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1056+1475C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188462 | |||||||
chr15:41188496 | G | A | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1056+1441C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188496 | |||||||
chr15:41188551 | C | T | 28 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1056+1386G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188551 | |||||||
chr15:41188600 | C | T | 64 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1056+1337G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188600 | |||||||
chr15:41188625 | T | G | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1056+1312A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188625 | |||||||
chr15:41188644 | G | A | 5 | a0001c0001t0004g0029 a0001c0001t0004g0045 a0001c0001t0004g0055 others(2): Show |
5 | HG02257.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1056+1293C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188644 | |||||||
chr15:41188682 | G | A | 1 | a0002c0004t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1056+1255C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188682 | |||||||
chr15:41188698 | C | G | 1 | a0001c0002t0001g0294 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1056+1239G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188698 | |||||||
chr15:41188782 | C | T | 1 | a0002c0003t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1056+1155G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188782 | |||||||
chr15:41188803 | CT | C | 168 | a0001c0001t0001g0018 a0001c0001t0002g0002 a0001c0001t0002g0089 others(165): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1056+1133delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188803 | |||||||
chr15:41188803 | CTT | C | 9 | a0001c0001t0003g0034 a0001c0002t0001g0041 a0001c0002t0001g0196 others(6): Show |
9 | HG01070.hp1 HG01192.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1056+1132_1056+113 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188803 | |||||||
chr15:41188910 | C | G | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1056+1027G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188910 | |||||||
chr15:41188930 | G | C | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+1007C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188930 | |||||||
chr15:41188990 | G | T | 7 | a0002c0003t0001g0115 a0002c0003t0001g0116 a0002c0003t0001g0121 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1056+947C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188990 | |||||||
chr15:41189056 | A | G | 129 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1056+881T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189056 | |||||||
chr15:41189222 | A | T | 134 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0002g0143 others(131): Show |
134 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1056+715T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189222 | |||||||
chr15:41189241 | G | A | 1 | a0002c0003t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1056+696C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189241 | |||||||
chr15:41189326 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1056+611G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189326 | |||||||
chr15:41189408 | A | G | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1056+529T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189408 | |||||||
chr15:41189478 | A | G | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+459T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189478 | |||||||
chr15:41189550 | T | C | 4 | a0001c0001t0002g0138 a0001c0001t0002g0145 a0001c0001t0002g0155 others(1): Show |
4 | HG01891.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+387A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189550 | |||||||
chr15:41189713 | T | C | 1 | a0008c0016t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1056+224A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189713 | |||||||
chr15:41189732 | TAGAC | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1056+201_1056+204d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189732 | |||||||
chr15:41189807 | C | T | 1 | a0001c0002t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1056+130G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189807 | |||||||
chr15:41189815 | A | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1056+122T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189815 | |||||||
chr15:41190187 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.865-59C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190187 | |||||||
chr15:41190267 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-139G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190267 | |||||||
chr15:41190367 | A | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0052 |
2 | NA18957.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.865-239T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190367 | |||||||
chr15:41190586 | C | A | 13 | a0001c0002t0001g0232 a0001c0002t0001g0234 a0001c0002t0001g0239 others(10): Show |
13 | HG01109.hp2 HG01123.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.865-458G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190586 | |||||||
chr15:41190602 | T | C | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.865-474A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190602 | |||||||
chr15:41190618 | C | T | 1 | a0002c0003t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.865-490G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190618 | |||||||
chr15:41190819 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.864+623C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190819 | |||||||
chr15:41190833 | A | C | 1 | a0001c0005t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.864+609T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190833 | |||||||
chr15:41190898 | GTTTA | G | 302 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(299): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.864+540_864+543del others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190898 | |||||||
chr15:41190906 | A | G | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.864+536T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190906 | |||||||
chr15:41191002 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.864+440G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191002 | |||||||
chr15:41191053 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.864+389C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191053 | |||||||
chr15:41191336 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.864+106T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191336 | |||||||
chr15:41191425 | A | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.864+17T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191425 | |||||||
chr15:41191433 | T | TA | 306 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(303): Show |
307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
splice_region_variant&intron_variant | LOW | c.864+8dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191433 | |||||||
chr15:41191803 | G | A | 6 | a0001c0002t0001g0213 a0001c0002t0001g0224 a0001c0002t0001g0315 others(3): Show |
6 | HG00609.hp2 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-218C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41191803 | |||||||
chr15:41191816 | G | A | 1 | a0001c0001t0004g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.721-231C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41191816 | |||||||
chr15:41192070 | T | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-485A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192070 | |||||||
chr15:41192089 | C | A | 182 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.721-504G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192089 | |||||||
chr15:41192116 | C | T | 28 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(25): Show |
28 | HG00408.hp1 HG01496.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-531G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192116 | |||||||
chr15:41192130 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-545G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192130 | |||||||
chr15:41192248 | C | A | 1 | a0001c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721-663G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192248 | |||||||
chr15:41192479 | T | C | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-894A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192479 | |||||||
chr15:41192506 | A | C | 1 | a0001c0001t0002g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.721-921T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192506 | |||||||
chr15:41192592 | GCAT | G | 8 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0209 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-1010_721-1008d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | |||||||
chr15:41192592 | GCATT | G | 33 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0199 others(30): Show |
33 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.721-1011_721-1008d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | |||||||
chr15:41192592 | GCATTT | G | 71 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(68): Show |
71 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.721-1012_721-1008d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | |||||||
chr15:41192592 | GCATTTT | G | 6 | a0001c0002t0001g0205 a0001c0002t0001g0282 a0001c0002t0001g0284 others(3): Show |
6 | HG00673.hp2 HG03098.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1013_721-1008d others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | |||||||
chr15:41192592 | GCATTTTT others(15): Show |
G | 1 | a0001c0001t0002g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1029_721-1008d others(24): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | |||||||
chr15:41192593 | C | T | 7 | a0001c0002t0001g0212 a0001c0002t0001g0242 a0001c0002t0001g0244 others(4): Show |
7 | HG00558.hp2 HG02523.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-1008G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192593 | |||||||
chr15:41192594 | A | ATTTT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG02109.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1013_721-1010d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | AT | A | 19 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0052 others(16): Show |
20 | HG01106.hp1 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1010delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATT | A | 40 | a0001c0001t0003g0034 a0001c0001t0003g0042 a0001c0001t0003g0043 others(37): Show |
40 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.721-1011_721-1010d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTT | A | 19 | a0001c0001t0003g0026 a0001c0001t0003g0033 a0001c0001t0003g0035 others(16): Show |
19 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.721-1012_721-1010d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTTTTTT others(3): Show |
A | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1019_721-1010d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTTTTTT others(6): Show |
A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1022_721-1010d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTTTTTT others(14): Show |
A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0180 |
2 | HG02027.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.721-1030_721-1010d others(23): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTTTTTT others(15): Show |
A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0130 a0001c0001t0002g0133 others(57): Show |
61 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.721-1031_721-1010d others(24): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192594 | ATTTTTTT others(16): Show |
A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.721-1032_721-1010d others(25): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | |||||||
chr15:41192596 | T | A | 2 | a0001c0002t0001g0208 a0001c0002t0001g0269 |
2 | HG03239.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.721-1011A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192596 | |||||||
chr15:41192597 | T | A | 8 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0209 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-1012A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192597 | |||||||
chr15:41192598 | T | A | 33 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0199 others(30): Show |
33 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.721-1013A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192598 | |||||||
chr15:41192599 | T | A | 71 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(68): Show |
71 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.721-1014A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192599 | |||||||
chr15:41192600 | T | A | 6 | a0001c0002t0001g0205 a0001c0002t0001g0282 a0001c0002t0001g0284 others(3): Show |
6 | HG00673.hp2 HG03098.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1015A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192600 | |||||||
chr15:41192606 | T | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.721-1021A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192606 | |||||||
chr15:41192611 | T | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.721-1026A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192611 | |||||||
chr15:41192616 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1031A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192616 | |||||||
chr15:41192689 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0167 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.721-1104T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192689 | |||||||
chr15:41192737 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1152G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192737 | |||||||
chr15:41192790 | AT | A | 156 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(153): Show |
157 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.721-1206delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192790 | |||||||
chr15:41192790 | ATT | A | 103 | a0001c0001t0002g0150 a0001c0001t0002g0166 a0001c0001t0002g0171 others(100): Show |
103 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.721-1207_721-1206d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192790 | |||||||
chr15:41192842 | C | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1257G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192842 | |||||||
chr15:41192952 | A | G | 18 | a0001c0002t0001g0232 a0001c0002t0001g0234 a0001c0002t0001g0239 others(15): Show |
18 | HG00609.hp1 HG01109.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-1367T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192952 | |||||||
chr15:41193011 | C | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-1426G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193011 | |||||||
chr15:41193028 | T | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1443A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193028 | |||||||
chr15:41193423 | A | G | 4 | a0002c0003t0005g0098 a0002c0003t0005g0099 a0002c0003t0005g0100 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1838T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193423 | |||||||
chr15:41193499 | G | A | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.721-1914C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193499 | |||||||
chr15:41193745 | C | CA | 139 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+2029dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193745 | |||||||
chr15:41193999 | A | AT | 59 | a0001c0002t0001g0113 a0001c0002t0001g0128 a0001c0002t0001g0198 others(56): Show |
59 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.720+1775dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | |||||||
chr15:41193999 | AT | A | 71 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.720+1775delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | |||||||
chr15:41193999 | ATT | A | 52 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(49): Show |
53 | HG00408.hp1 HG01081.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.720+1774_720+1775d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | |||||||
chr15:41194046 | C | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0058 |
2 | HG02027.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.720+1729G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194046 | |||||||
chr15:41194059 | T | C | 132 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(129): Show |
132 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.720+1716A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194059 | |||||||
chr15:41194081 | A | G | 273 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(270): Show |
274 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.720+1694T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194081 | |||||||
chr15:41194195 | T | C | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+1580A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194195 | |||||||
chr15:41194226 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.720+1549A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194226 | |||||||
chr15:41194241 | G | A | 2 | a0001c0001t0002g0166 a0001c0001t0002g0181 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.720+1534C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194241 | |||||||
chr15:41194306 | G | A | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+1469C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194306 | |||||||
chr15:41194319 | G | A | 1 | a0001c0002t0001g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.720+1456C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194319 | |||||||
chr15:41194334 | A | C | 1 | a0002c0003t0001g0092 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.720+1441T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194334 | |||||||
chr15:41194452 | G | C | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1323C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194452 | |||||||
chr15:41194573 | A | C | 7 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+1202T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194573 | |||||||
chr15:41194709 | A | G | 2 | a0001c0002t0001g0207 a0001c0002t0001g0209 |
2 | HG01081.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.720+1066T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194709 | |||||||
chr15:41194781 | A | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+994T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194781 | |||||||
chr15:41194792 | G | A | 6 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(3): Show |
6 | HG00323.hp2 HG00738.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+983C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194792 | |||||||
chr15:41195231 | TAAC | T | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+541_720+543del others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195231 | |||||||
chr15:41195285 | C | T | 4 | a0001c0001t0002g0141 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | NA18939.hp1 NA18956.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+490G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195285 | |||||||
chr15:41195318 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.720+457G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195318 | |||||||
chr15:41195348 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.720+427A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195348 | |||||||
chr15:41195584 | G | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0048 |
2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.720+191C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195584 | |||||||
chr15:41195663 | C | CA | 174 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.720+111dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195663 | |||||||
chr15:41195663 | CA | C | 8 | a0001c0002t0001g0227 a0001c0002t0001g0237 a0001c0002t0001g0240 others(5): Show |
8 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+111delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195663 | |||||||
chr15:41195697 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+78G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195697 | |||||||
chr15:41195736 | G | C | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+39C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195736 | |||||||
chr15:41196119 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.535-82G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196119 | |||||||
chr15:41196120 | G | A | 1 | a0004c0014t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-83C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196120 | |||||||
chr15:41196207 | C | T | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.535-170G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196207 | |||||||
chr15:41196312 | A | AT | 59 | a0001c0001t0003g0044 a0001c0001t0004g0012 a0001c0001t0004g0029 others(56): Show |
59 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.535-276dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | |||||||
chr15:41196312 | A | ATT | 58 | a0001c0001t0001g0018 a0001c0001t0003g0011 a0001c0001t0003g0026 others(55): Show |
58 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.535-277_535-276dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | |||||||
chr15:41196312 | A | ATTT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02027.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.535-278_535-276dup others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | |||||||
chr15:41196312 | ATTTTT | A | 62 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(59): Show |
63 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.535-280_535-276del others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | |||||||
chr15:41196628 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.535-591T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196628 | |||||||
chr15:41196940 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-903G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196940 | |||||||
chr15:41197105 | G | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1068C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197105 | |||||||
chr15:41197293 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.535-1256A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197293 | |||||||
chr15:41197368 | A | G | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1331T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197368 | |||||||
chr15:41197376 | T | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1339A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197376 | |||||||
chr15:41197388 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1351G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197388 | |||||||
chr15:41197657 | T | A | 1 | a0001c0002t0001g0222 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535-1620A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197657 | |||||||
chr15:41197796 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.535-1759A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197796 | |||||||
chr15:41197814 | T | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
142 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.535-1777A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197814 | |||||||
chr15:41197835 | A | C | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1798T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197835 | |||||||
chr15:41197836 | G | T | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1799C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197836 | |||||||
chr15:41197837 | G | C | 65 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.535-1800C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197837 | |||||||
chr15:41197837 | G | GGTTAAGC others(294): Show |
1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1801_535-1800i others(303): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197837 | |||||||
chr15:41198101 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0134 a0001c0001t0002g0135 others(30): Show |
34 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.535-2064C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198101 | |||||||
chr15:41198256 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.535-2219C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198256 | |||||||
chr15:41198291 | C | T | 1 | a0001c0002t0001g0310 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.535-2254G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198291 | |||||||
chr15:41198335 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.535-2298C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198335 | |||||||
chr15:41198344 | G | A | 1 | a0001c0002t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.535-2307C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198344 | |||||||
chr15:41198376 | A | G | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-2339T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198376 | |||||||
chr15:41198473 | C | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.535-2436G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198473 | |||||||
chr15:41198490 | A | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0053 others(1): Show |
4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2453T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198490 | |||||||
chr15:41198491 | A | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0053 others(1): Show |
4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2454T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198491 | |||||||
chr15:41198637 | C | T | 78 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(75): Show |
78 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.535-2600G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198637 | |||||||
chr15:41198657 | C | G | 1 | a0001c0002t0008g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.535-2620G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198657 | |||||||
chr15:41198700 | T | TA | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.535-2664dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198700 | |||||||
chr15:41198706 | A | C | 1 | a0002c0004t0001g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.535-2669T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198706 | |||||||
chr15:41198708 | A | T | 3 | a0001c0002t0001g0269 a0001c0002t0001g0291 a0001c0005t0001g0095 |
3 | HG02922.hp2 HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.535-2671T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198708 | |||||||
chr15:41198708 | AT | A | 6 | a0001c0002t0001g0228 a0002c0003t0001g0009 a0002c0003t0001g0091 others(3): Show |
6 | HG01070.hp2 HG01515.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-2672delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198708 | |||||||
chr15:41198709 | T | A | 96 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.535-2672A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198709 | |||||||
chr15:41198710 | T | A | 8 | a0001c0001t0004g0072 a0001c0002t0014g0094 a0002c0003t0001g0009 others(5): Show |
8 | HG01515.hp1 HG02074.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-2673A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198710 | |||||||
chr15:41198782 | T | C | 182 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.535-2745A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198782 | |||||||
chr15:41198829 | T | C | 181 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.535-2792A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198829 | |||||||
chr15:41198862 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535-2825G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198862 | |||||||
chr15:41198879 | G | T | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-2842C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198879 | |||||||
chr15:41199248 | G | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.535-3211C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199248 | |||||||
chr15:41199267 | A | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3230T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199267 | |||||||
chr15:41199334 | C | A | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-3297G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199334 | |||||||
chr15:41199412 | T | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3375A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199412 | |||||||
chr15:41199458 | A | G | 186 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.535-3421T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199458 | |||||||
chr15:41199595 | ATATATAT | A | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-3565_535-3559d others(9): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199595 | |||||||
chr15:41199705 | A | ATC | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.535-3670_535-3669d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199705 | |||||||
chr15:41199711 | T | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-3674A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199711 | |||||||
chr15:41199728 | A | ATC | 128 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(125): Show |
128 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.535-3692_535-3691i others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199728 | |||||||
chr15:41199730 | G | C | 275 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(272): Show |
276 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.535-3693C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199730 | |||||||
chr15:41199732 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3695A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199732 | |||||||
chr15:41199737 | ATG | A | 64 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(61): Show |
65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3702_535-3701d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199737 | |||||||
chr15:41199739 | GTC | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3704_535-3703d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199739 | |||||||
chr15:41199740 | T | A | 200 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(197): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.535-3703A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199740 | |||||||
chr15:41199741 | C | T | 200 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(197): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.535-3704G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199741 | |||||||
chr15:41199746 | A | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3709T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199746 | |||||||
chr15:41199748 | T | C | 200 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(197): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.535-3711A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199748 | |||||||
chr15:41199748 | T | G | 64 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(61): Show |
65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3711A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199748 | |||||||
chr15:41199753 | A | G | 2 | a0001c0002t0001g0203 a0001c0002t0001g0204 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.535-3716T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199753 | |||||||
chr15:41199755 | G | A | 64 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(61): Show |
65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3718C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199755 | |||||||
chr15:41199755 | G | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3718C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199755 | |||||||
chr15:41199757 | T | TATATAAT others(72): Show |
3 | a0001c0001t0003g0011 a0001c0001t0003g0051 a0001c0001t0003g0088 |
3 | NA18984.hp1 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(81): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(74): Show |
1 | a0001c0002t0001g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(83): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(37): Show |
2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(46): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(51): Show |
62 | a0001c0001t0003g0026 a0001c0001t0003g0030 a0001c0001t0003g0031 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(60): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(51): Show |
4 | a0001c0002t0001g0305 a0001c0005t0001g0095 a0001c0005t0001g0096 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(60): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(74): Show |
110 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(107): Show |
110 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(83): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(97): Show |
1 | a0001c0002t0001g0222 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(97): Show |
14 | a0001c0002t0001g0208 a0001c0002t0001g0224 a0001c0002t0001g0233 others(11): Show |
14 | HG00408.hp2 HG00544.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATAAT others(120): Show |
1 | a0001c0002t0001g0241 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(129): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATATC others(113): Show |
1 | a0001c0002t0001g0298 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(122): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATCAT others(44): Show |
1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(53): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATCAT others(42): Show |
61 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(58): Show |
62 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(51): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATCAT others(37): Show |
2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(46): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATGAT others(90): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(99): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATGAT others(92): Show |
1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(101): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATGAT others(106): Show |
1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(115): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199757 | T | TATATTAT others(97): Show |
1 | a0001c0002t0001g0294 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | |||||||
chr15:41199759 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3722G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199759 | |||||||
chr15:41199764 | A | G | 5 | a0001c0002t0001g0226 a0001c0002t0001g0240 a0001c0002t0001g0274 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.535-3727T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199764 | |||||||
chr15:41199766 | G | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3729C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199766 | |||||||
chr15:41199768 | T | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3731A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199768 | |||||||
chr15:41199777 | C | G | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0189 |
3 | NA19005.hp1 NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.535-3740G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199777 | |||||||
chr15:41199785 | A | C | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3748T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199785 | |||||||
chr15:41199811 | T | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3774A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199811 | |||||||
chr15:41199812 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3775G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199812 | |||||||
chr15:41199820 | G | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3783C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199820 | |||||||
chr15:41199822 | T | TATA | 305 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.535-3788_535-3786d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199822 | |||||||
chr15:41199839 | T | C | 2 | a0002c0003t0001g0010 a0002c0003t0001g0106 |
2 | HG00642.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.535-3802A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199839 | |||||||
chr15:41199865 | C | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3828G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199865 | |||||||
chr15:41199867 | G | A | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3830C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199867 | |||||||
chr15:41199897 | A | G | 11 | a0001c0001t0002g0144 a0001c0001t0002g0170 a0001c0001t0002g0179 others(8): Show |
11 | HG00609.hp1 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3860T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199897 | |||||||
chr15:41200048 | C | T | 9 | a0001c0002t0014g0094 a0002c0004t0001g0001 a0002c0004t0001g0006 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-4011G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200048 | |||||||
chr15:41200085 | G | T | 186 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.535-4048C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200085 | |||||||
chr15:41200092 | G | A | 28 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.535-4055C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200092 | |||||||
chr15:41200137 | G | A | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-4100C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200137 | |||||||
chr15:41200186 | A | C | 1 | a0001c0002t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.535-4149T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200186 | |||||||
chr15:41200459 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.535-4422C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200459 | |||||||
chr15:41200771 | T | C | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-4734A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200771 | |||||||
chr15:41200815 | T | C | 303 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(300): Show |
304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.535-4778A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200815 | |||||||
chr15:41200879 | A | AT | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
83 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.535-4843dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200879 | |||||||
chr15:41200943 | G | A | 3 | a0001c0002t0001g0309 a0001c0002t0001g0310 a0001c0002t0001g0311 |
3 | HG01943.hp1 HG01952.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.535-4906C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200943 | |||||||
chr15:41200945 | C | A | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.535-4908G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200945 | |||||||
chr15:41201116 | T | G | 4 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0053 others(1): Show |
4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5079A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201116 | |||||||
chr15:41201162 | C | T | 1 | a0001c0002t0002g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.535-5125G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201162 | |||||||
chr15:41201259 | C | G | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-5222G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201259 | |||||||
chr15:41201485 | AT | A | 56 | a0001c0001t0002g0141 a0001c0001t0002g0168 a0001c0001t0002g0175 others(53): Show |
56 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.535-5449delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | |||||||
chr15:41201485 | ATT | A | 232 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(229): Show |
232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.535-5450_535-5449d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | |||||||
chr15:41201485 | ATTT | A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0157 a0001c0001t0002g0174 others(11): Show |
15 | HG01081.hp1 HG01106.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-5451_535-5449d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | |||||||
chr15:41201521 | G | A | 64 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(61): Show |
64 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.535-5484C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201521 | |||||||
chr15:41201590 | A | T | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-5553T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201590 | |||||||
chr15:41201909 | T | C | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.535-5872A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201909 | |||||||
chr15:41202066 | G | A | 1 | a0007c0010t0002g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.535-6029C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202066 | |||||||
chr15:41202088 | C | G | 1 | a0001c0002t0001g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.535-6051G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202088 | |||||||
chr15:41202148 | T | TTA | 6 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(3): Show |
6 | HG00642.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-6113_535-6112d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202148 | |||||||
chr15:41202148 | TTA | T | 129 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(126): Show |
130 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.535-6113_535-6112d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202148 | |||||||
chr15:41202153 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.535-6116A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202153 | |||||||
chr15:41202155 | T | C | 62 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(59): Show |
63 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.535-6118A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202155 | |||||||
chr15:41202164 | A | AT | 6 | a0001c0002t0001g0193 a0001c0002t0001g0280 a0001c0002t0001g0310 others(3): Show |
6 | HG00597.hp2 HG01943.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-6128dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202164 | |||||||
chr15:41202164 | A | T | 10 | a0001c0002t0001g0207 a0001c0002t0001g0214 a0001c0002t0001g0270 others(7): Show |
10 | HG00639.hp2 HG01081.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-6127T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202164 | |||||||
chr15:41202166 | A | AT | 26 | a0001c0002t0001g0041 a0001c0002t0001g0128 a0001c0002t0001g0196 others(23): Show |
26 | HG00609.hp2 HG00673.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.535-6130dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | |||||||
chr15:41202166 | A | T | 134 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(131): Show |
135 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.535-6129T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | |||||||
chr15:41202166 | AT | A | 4 | a0001c0001t0002g0189 a0001c0005t0001g0095 a0001c0005t0001g0096 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-6130delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | |||||||
chr15:41202166 | ATT | A | 12 | a0001c0001t0003g0033 a0001c0001t0003g0039 a0001c0001t0003g0042 others(9): Show |
12 | HG01928.hp2 HG01975.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.535-6131_535-6130d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | |||||||
chr15:41202168 | T | A | 24 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0002c0003t0001g0010 others(21): Show |
24 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.535-6131A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202168 | |||||||
chr15:41202170 | T | A | 3 | a0002c0003t0001g0102 a0002c0003t0001g0111 a0002c0003t0001g0118 |
3 | HG01975.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.535-6133A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202170 | |||||||
chr15:41202174 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.535-6137A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202174 | |||||||
chr15:41202185 | T | A | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-6148A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202185 | |||||||
chr15:41202445 | A | G | 1 | a0001c0002t0011g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.535-6408T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202445 | |||||||
chr15:41202466 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-6429G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202466 | |||||||
chr15:41202475 | C | CAT | 3 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 |
3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.535-6440_535-6439d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202475 | |||||||
chr15:41202566 | T | C | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-6529A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202566 | |||||||
chr15:41202682 | G | A | 3 | a0002c0003t0001g0115 a0002c0003t0001g0125 a0002c0003t0001g0127 |
3 | HG00099.hp2 HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.535-6645C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202682 | |||||||
chr15:41202713 | C | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-6676G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202713 | |||||||
chr15:41202772 | G | A | 16 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0031 others(13): Show |
16 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+6729C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202772 | |||||||
chr15:41202825 | C | T | 28 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0131 others(25): Show |
28 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.534+6676G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202825 | |||||||
chr15:41202917 | C | CA | 22 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0173 others(19): Show |
22 | HG00673.hp2 HG01243.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.534+6583dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | |||||||
chr15:41202917 | CA | C | 9 | a0001c0001t0002g0163 a0001c0001t0003g0034 a0001c0002t0001g0193 others(6): Show |
9 | HG00597.hp2 HG00609.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.534+6583delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | |||||||
chr15:41202917 | CAA | C | 32 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(29): Show |
33 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.534+6582_534+6583d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | |||||||
chr15:41202918 | A | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0153 others(1): Show |
4 | HG02040.hp1 NA18942.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+6583T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202918 | |||||||
chr15:41203206 | A | G | 307 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.534+6295T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203206 | |||||||
chr15:41203262 | C | T | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.534+6239G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203262 | |||||||
chr15:41203333 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+6168G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203333 | |||||||
chr15:41203542 | A | G | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.534+5959T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203542 | |||||||
chr15:41203734 | T | A | 40 | a0001c0005t0001g0107 a0002c0003t0001g0009 a0002c0003t0001g0010 others(37): Show |
41 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.534+5767A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203734 | |||||||
chr15:41203825 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0167 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.534+5676C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203825 | |||||||
chr15:41203871 | C | T | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+5630G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203871 | |||||||
chr15:41203876 | C | T | 1 | a0001c0001t0004g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.534+5625G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203876 | |||||||
chr15:41203916 | C | CA | 49 | a0001c0002t0001g0041 a0001c0002t0001g0112 a0001c0002t0001g0113 others(46): Show |
49 | HG00323.hp2 HG00597.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+5584dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAA | 7 | a0001c0002t0001g0281 a0001c0002t0001g0294 a0002c0003t0001g0010 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+5583_534+5584d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAA | 16 | a0001c0001t0003g0040 a0001c0001t0003g0061 a0001c0005t0001g0107 others(13): Show |
16 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.534+5582_534+5584d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAA | 42 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.534+5581_534+5584d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAA | 46 | a0001c0001t0002g0002 a0001c0001t0002g0134 a0001c0001t0002g0138 others(43): Show |
47 | HG00673.hp1 HG01081.hp1 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.534+5580_534+5584d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAA | 18 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0143 others(15): Show |
18 | HG00408.hp1 HG01106.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+5579_534+5584d others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01169.hp2 HG01433.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+5577_534+5584d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAAA others(2): Show |
18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
18 | HG01175.hp2 HG02027.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+5576_534+5584d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(4): Show |
7 | HG01884.hp1 HG02071.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+5575_534+5584d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0168 a0001c0001t0002g0181 |
2 | HG02055.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.534+5574_534+5584d others(13): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.534+5572_534+5584d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203916 | CAAAAAAA others(5): Show |
C | 3 | a0002c0003t0001g0115 a0002c0003t0001g0125 a0002c0003t0001g0127 |
3 | HG00099.hp2 HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.534+5573_534+5584d others(14): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | |||||||
chr15:41203973 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534+5528G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203973 | |||||||
chr15:41204068 | C | A | 307 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.534+5433G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204068 | |||||||
chr15:41204141 | G | A | 1 | a0001c0002t0011g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.534+5360C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204141 | |||||||
chr15:41204226 | C | T | 11 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.534+5275G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204226 | |||||||
chr15:41204237 | G | GACTCTGT others(6): Show |
1 | a0001c0001t0003g0075 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.534+5251_534+5263d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204237 | |||||||
chr15:41204247 | C | CA | 33 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00642.hp1 HG00642.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.534+5253dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | |||||||
chr15:41204247 | C | CAAAAAAA others(294): Show |
1 | a0001c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.534+5253_534+5254i others(303): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | |||||||
chr15:41204247 | CA | C | 68 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0131 others(65): Show |
69 | HG00408.hp1 HG00639.hp1 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.534+5253delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | |||||||
chr15:41204320 | G | A | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.534+5181C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204320 | |||||||
chr15:41204380 | G | C | 1 | a0001c0002t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534+5121C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204380 | |||||||
chr15:41204466 | G | A | 21 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(18): Show |
21 | HG00408.hp1 HG02040.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.534+5035C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204466 | |||||||
chr15:41204515 | C | T | 54 | a0001c0002t0001g0114 a0001c0002t0001g0191 a0001c0002t0001g0192 others(51): Show |
54 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.534+4986G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204515 | |||||||
chr15:41204530 | A | G | 274 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(271): Show |
275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.534+4971T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204530 | |||||||
chr15:41204759 | C | CAT | 5 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(2): Show |
5 | HG01106.hp1 HG01515.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+4740_534+4741d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204759 | |||||||
chr15:41204797 | G | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+4704C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204797 | |||||||
chr15:41204882 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+4619G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204882 | |||||||
chr15:41205032 | T | C | 1 | a0001c0002t0001g0262 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.534+4469A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205032 | |||||||
chr15:41205212 | C | T | 3 | a0001c0002t0001g0193 a0001c0002t0001g0219 a0001c0002t0001g0220 |
3 | HG00597.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.534+4289G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205212 | |||||||
chr15:41205229 | T | C | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+4272A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205229 | |||||||
chr15:41205332 | C | A | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+4169G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205332 | |||||||
chr15:41205387 | G | A | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.534+4114C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205387 | |||||||
chr15:41205392 | A | C | 1 | a0002c0003t0001g0009 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.534+4109T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205392 | |||||||
chr15:41205436 | CTGTA | C | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+4061_534+4064d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205436 | |||||||
chr15:41205467 | T | G | 1 | a0001c0002t0001g0269 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.534+4034A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205467 | |||||||
chr15:41205548 | T | C | 2 | a0001c0002t0006g0003 a0001c0002t0006g0004 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.534+3953A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205548 | |||||||
chr15:41205605 | C | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+3896G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205605 | |||||||
chr15:41205702 | GGAAGGAG others(9): Show |
G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
76 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.534+3783_534+3798d others(18): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205702 | |||||||
chr15:41205710 | GGAAGGAG others(1): Show |
G | 64 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(61): Show |
65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.534+3783_534+3790d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205710 | |||||||
chr15:41205718 | A | G | 47 | a0001c0002t0014g0094 a0001c0005t0001g0007 a0001c0005t0001g0008 others(44): Show |
48 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.534+3783T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205718 | |||||||
chr15:41205721 | A | G | 7 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+3780T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205721 | |||||||
chr15:41205805 | G | A | 1 | a0001c0002t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.534+3696C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205805 | |||||||
chr15:41205853 | G | T | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+3648C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205853 | |||||||
chr15:41205879 | C | CT | 18 | a0001c0001t0002g0141 a0001c0001t0002g0150 a0001c0001t0002g0151 others(15): Show |
18 | HG00099.hp1 HG00673.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.534+3621dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205879 | |||||||
chr15:41205956 | T | C | 2 | a0001c0001t0004g0069 a0001c0001t0004g0070 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.534+3545A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205956 | |||||||
chr15:41205980 | A | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.534+3521T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205980 | |||||||
chr15:41206175 | ACAGGAAA others(90): Show |
A | 1 | a0001c0002t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.534+3229_534+3325d others(99): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206175 | |||||||
chr15:41206261 | G | C | 1 | a0001c0002t0001g0235 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.534+3240C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206261 | |||||||
chr15:41206474 | GA | G | 7 | a0001c0001t0003g0074 a0001c0002t0001g0212 a0001c0002t0001g0227 others(4): Show |
7 | HG00639.hp2 HG00738.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+3026delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | |||||||
chr15:41206474 | GAA | G | 62 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(59): Show |
62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.534+3025_534+3026d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | |||||||
chr15:41206474 | GAAA | G | 77 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
78 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.534+3024_534+3026d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | |||||||
chr15:41206618 | C | CT | 118 | a0001c0002t0001g0113 a0001c0002t0001g0114 a0001c0002t0001g0128 others(115): Show |
118 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.534+2882dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | |||||||
chr15:41206618 | C | CTT | 12 | a0001c0002t0001g0112 a0001c0002t0001g0200 a0001c0002t0001g0222 others(9): Show |
12 | HG01175.hp1 HG02074.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.534+2881_534+2882d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | |||||||
chr15:41206618 | CTT | C | 6 | a0001c0001t0002g0153 a0001c0001t0002g0181 a0001c0001t0015g0316 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+2881_534+2882d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | |||||||
chr15:41206618 | CTTT | C | 134 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(131): Show |
135 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.534+2880_534+2882d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | |||||||
chr15:41206691 | G | A | 1 | a0001c0002t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.534+2810C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206691 | |||||||
chr15:41206754 | T | C | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.534+2747A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206754 | |||||||
chr15:41206756 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.534+2745C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206756 | |||||||
chr15:41206771 | G | A | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.534+2730C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206771 | |||||||
chr15:41206870 | G | T | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2631C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206870 | |||||||
chr15:41206890 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.534+2611C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206890 | |||||||
chr15:41206929 | CT | C | 39 | a0001c0002t0001g0114 a0001c0002t0001g0214 a0001c0002t0001g0244 others(36): Show |
39 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.534+2571delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | |||||||
chr15:41206929 | CTT | C | 124 | a0001c0001t0001g0022 a0001c0001t0002g0089 a0001c0001t0002g0133 others(121): Show |
124 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.534+2570_534+2571d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | |||||||
chr15:41206929 | CTTT | C | 131 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(128): Show |
132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.534+2569_534+2571d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | |||||||
chr15:41206929 | CTTTT | C | 11 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0143 others(8): Show |
11 | HG00099.hp1 HG01167.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+2568_534+2571d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | |||||||
chr15:41206954 | T | A | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2547A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206954 | |||||||
chr15:41206966 | C | T | 52 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(49): Show |
52 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.534+2535G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206966 | |||||||
chr15:41206969 | C | G | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2532G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206969 | |||||||
chr15:41206994 | G | T | 5 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+2507C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206994 | |||||||
chr15:41207082 | A | C | 1 | a0001c0002t0001g0294 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.534+2419T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207082 | |||||||
chr15:41207097 | C | T | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2404G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207097 | |||||||
chr15:41207102 | G | T | 1 | a0001c0002t0001g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.534+2399C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207102 | |||||||
chr15:41207110 | G | A | 1 | a0001c0002t0009g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.534+2391C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207110 | |||||||
chr15:41207151 | G | A | 65 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.534+2350C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207151 | |||||||
chr15:41207358 | A | T | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2143T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207358 | |||||||
chr15:41207455 | T | G | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2046A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207455 | |||||||
chr15:41207529 | C | G | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1972G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207529 | |||||||
chr15:41207536 | T | C | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1965A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207536 | |||||||
chr15:41207550 | A | T | 29 | a0001c0002t0001g0128 a0001c0002t0001g0193 a0001c0002t0001g0196 others(26): Show |
29 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.534+1951T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207550 | |||||||
chr15:41207605 | T | C | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1896A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207605 | |||||||
chr15:41208002 | C | G | 3 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 |
3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.534+1499G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208002 | |||||||
chr15:41208010 | C | CA | 7 | a0001c0001t0001g0022 a0001c0002t0001g0315 a0001c0005t0001g0095 others(4): Show |
7 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+1490dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208010 | |||||||
chr15:41208010 | CA | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(64): Show |
68 | HG00408.hp1 HG01070.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.534+1490delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208010 | |||||||
chr15:41208032 | G | A | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1469C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208032 | |||||||
chr15:41208056 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.534+1445A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208056 | |||||||
chr15:41208083 | C | G | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1418G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208083 | |||||||
chr15:41208145 | G | T | 3 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 |
3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.534+1356C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208145 | |||||||
chr15:41208163 | G | T | 28 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+1338C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208163 | |||||||
chr15:41208351 | T | G | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1150A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208351 | |||||||
chr15:41208369 | G | A | 5 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+1132C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | |||||||
chr15:41208369 | G | GA | 8 | a0001c0002t0001g0204 a0001c0002t0001g0263 a0001c0002t0001g0302 others(5): Show |
8 | HG01515.hp1 HG02074.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+1131dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | |||||||
chr15:41208369 | GA | G | 9 | a0001c0002t0001g0205 a0001c0002t0001g0228 a0001c0002t0001g0240 others(6): Show |
9 | HG01070.hp2 HG01943.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.534+1131delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | |||||||
chr15:41208369 | GAAA | G | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
134 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.534+1129_534+1131d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | |||||||
chr15:41208369 | GAAAA | G | 6 | a0001c0001t0002g0174 a0001c0001t0002g0184 a0001c0001t0003g0026 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+1128_534+1131d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | |||||||
chr15:41208442 | A | G | 65 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.534+1059T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208442 | |||||||
chr15:41208621 | G | A | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.534+880C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208621 | |||||||
chr15:41208727 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+774C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208727 | |||||||
chr15:41208809 | A | G | 1 | a0001c0001t0003g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.534+692T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208809 | |||||||
chr15:41208987 | T | TA | 151 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(148): Show |
153 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.534+513dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208987 | |||||||
chr15:41209192 | A | G | 209 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.534+309T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209192 | |||||||
chr15:41209285 | T | C | 156 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(153): Show |
158 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.534+216A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209285 | |||||||
chr15:41209323 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.534+178C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209323 | |||||||
chr15:41209778 | C | CT | 229 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(226): Show |
230 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.448-192dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209778 | |||||||
chr15:41209870 | T | C | 1 | a0001c0002t0001g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.448-283A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209870 | |||||||
chr15:41209946 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.448-359A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209946 | |||||||
chr15:41210150 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-563T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210150 | |||||||
chr15:41210180 | G | T | 11 | a0001c0001t0004g0005 a0001c0001t0004g0063 a0001c0001t0004g0064 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.448-593C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210180 | |||||||
chr15:41210183 | G | C | 1 | a0001c0008t0001g0300 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.448-596C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210183 | |||||||
chr15:41210377 | C | T | 1 | a0001c0002t0001g0041 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.448-790G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210377 | |||||||
chr15:41210393 | C | T | 4 | a0001c0001t0002g0141 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | NA18939.hp1 NA18956.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-806G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210393 | |||||||
chr15:41210417 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.448-830G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210417 | |||||||
chr15:41210662 | T | TA | 69 | a0001c0001t0002g0136 a0001c0001t0002g0173 a0001c0001t0003g0011 others(66): Show |
69 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.448-1076dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210662 | |||||||
chr15:41210662 | T | TAA | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.448-1077_448-1076d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210662 | |||||||
chr15:41210693 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.448-1106C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210693 | |||||||
chr15:41210828 | T | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1241A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210828 | |||||||
chr15:41210830 | C | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1243G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210830 | |||||||
chr15:41210932 | G | A | 2 | a0001c0002t0001g0203 a0001c0002t0001g0204 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.448-1345C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210932 | |||||||
chr15:41211000 | A | C | 18 | a0002c0003t0001g0103 a0002c0003t0001g0104 a0002c0003t0001g0110 others(15): Show |
18 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-1413T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211000 | |||||||
chr15:41211038 | C | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1451G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211038 | |||||||
chr15:41211100 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.448-1513G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211100 | |||||||
chr15:41211397 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1810G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211397 | |||||||
chr15:41211469 | T | A | 1 | a0001c0002t0001g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.448-1882A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211469 | |||||||
chr15:41211484 | T | A | 5 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1897A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211484 | |||||||
chr15:41211489 | A | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1902T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211489 | |||||||
chr15:41211508 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1921T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211508 | |||||||
chr15:41211532 | C | T | 170 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0131 others(167): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.448-1945G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211532 | |||||||
chr15:41211608 | A | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2021T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211608 | |||||||
chr15:41211620 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2033G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211620 | |||||||
chr15:41211704 | A | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0229 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.448-2117T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211704 | |||||||
chr15:41211795 | T | TAAAAAAA others(1): Show |
9 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(6): Show |
9 | HG00099.hp1 HG00558.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-2216_448-2209d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | |||||||
chr15:41211795 | T | TAAAAAAA others(2): Show |
70 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
71 | HG00544.hp1 HG00673.hp1 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.448-2217_448-2209d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | |||||||
chr15:41211795 | T | TAAAAAAA others(3): Show |
5 | a0001c0001t0003g0087 a0001c0001t0004g0065 a0001c0011t0001g0071 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-2218_448-2209d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | |||||||
chr15:41211795 | TA | T | 30 | a0001c0001t0002g0131 a0001c0001t0002g0134 a0001c0001t0002g0138 others(27): Show |
30 | HG00099.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.448-2209delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | |||||||
chr15:41212032 | CA | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2446delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212032 | |||||||
chr15:41212041 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2454T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212041 | |||||||
chr15:41212246 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.448-2659C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212246 | |||||||
chr15:41212265 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.448-2678G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212265 | |||||||
chr15:41212277 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0018 others(6): Show |
9 | HG02109.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-2690C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212277 | |||||||
chr15:41212387 | A | G | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.448-2800T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212387 | |||||||
chr15:41212454 | C | CA | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.448-2868dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212454 | |||||||
chr15:41212535 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2948C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212535 | |||||||
chr15:41212704 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.447+3071C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212704 | |||||||
chr15:41213047 | A | T | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.447+2728T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213047 | |||||||
chr15:41213049 | T | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+2726A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213049 | |||||||
chr15:41213211 | A | AT | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2563dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213211 | |||||||
chr15:41213457 | G | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2318C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213457 | |||||||
chr15:41213501 | T | TTTTTGTT others(3): Show |
1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447+2264_447+2273d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | |||||||
chr15:41213501 | T | TTTTTGTT others(8): Show |
13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG02109.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2259_447+2273d others(17): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | |||||||
chr15:41213501 | T | TTTTTGTT others(13): Show |
13 | a0001c0001t0001g0023 a0001c0001t0003g0081 a0001c0001t0004g0012 others(10): Show |
13 | HG00673.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2254_447+2273d others(22): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | |||||||
chr15:41213501 | T | TTTTTGTT others(18): Show |
55 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0031 others(52): Show |
56 | HG00544.hp1 HG00558.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.447+2249_447+2273d others(27): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | |||||||
chr15:41213501 | T | TTTTTGTT others(23): Show |
2 | a0001c0001t0003g0026 a0001c0001t0004g0028 |
2 | HG00099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.447+2273_447+2274i others(32): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | |||||||
chr15:41213540 | C | CA | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2234dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213540 | |||||||
chr15:41213584 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2191G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213584 | |||||||
chr15:41213603 | C | T | 65 | a0001c0001t0003g0011 a0001c0001t0003g0026 a0001c0001t0003g0030 others(62): Show |
65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.447+2172G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213603 | |||||||
chr15:41213629 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2146T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213629 | |||||||
chr15:41213697 | C | T | 1 | a0001c0002t0009g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.447+2078G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213697 | |||||||
chr15:41213839 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1936G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213839 | |||||||
chr15:41213851 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1924T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213851 | |||||||
chr15:41213937 | A | G | 7 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.447+1838T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213937 | |||||||
chr15:41214036 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1739T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214036 | |||||||
chr15:41214098 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1677A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214098 | |||||||
chr15:41214143 | G | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.447+1632C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214143 | |||||||
chr15:41214276 | G | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1499C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214276 | |||||||
chr15:41214288 | A | G | 1 | a0001c0002t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.447+1487T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214288 | |||||||
chr15:41214311 | G | A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.447+1464C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214311 | |||||||
chr15:41214421 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1354C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214421 | |||||||
chr15:41214428 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.447+1347C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214428 | |||||||
chr15:41214475 | C | T | 1 | a0001c0002t0002g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.447+1300G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214475 | |||||||
chr15:41214512 | CA | C | 87 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(84): Show |
88 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.447+1262delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214512 | |||||||
chr15:41214598 | C | G | 10 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(7): Show |
10 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.447+1177G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214598 | |||||||
chr15:41214665 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.447+1110C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214665 | |||||||
chr15:41214689 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447+1086T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214689 | |||||||
chr15:41214904 | C | T | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.447+871G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214904 | |||||||
chr15:41214938 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+837C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214938 | |||||||
chr15:41214992 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+783C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214992 | |||||||
chr15:41215025 | G | A | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.447+750C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215025 | |||||||
chr15:41215113 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+662G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215113 | |||||||
chr15:41215270 | C | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+505G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215270 | |||||||
chr15:41215271 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+504C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215271 | |||||||
chr15:41215452 | C | T | 3 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 |
3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.447+323G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215452 | |||||||
chr15:41215457 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+318G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215457 | |||||||
chr15:41215461 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+314A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215461 | |||||||
chr15:41215579 | G | A | 6 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(3): Show |
6 | HG00642.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+196C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215579 | |||||||
chr15:41215667 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+108A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215667 | |||||||
chr15:41215685 | C | CA | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+89dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215685 | |||||||
chr15:41215685 | C | CAA | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+88_447+89dupTT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215685 | |||||||
chr15:41215839 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.389-6T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41215839 | |||||||
chr15:41215972 | G | C | 10 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(7): Show |
10 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.389-139C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41215972 | |||||||
chr15:41216012 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.389-179G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216012 | |||||||
chr15:41216056 | T | C | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.389-223A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216056 | |||||||
chr15:41216230 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.389-397T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216230 | |||||||
chr15:41216304 | T | TA | 72 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.388+363dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216304 | |||||||
chr15:41216304 | TA | T | 9 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(6): Show |
9 | HG01167.hp2 HG01515.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+363delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216304 | |||||||
chr15:41216319 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+349C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216319 | |||||||
chr15:41216321 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+347C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216321 | |||||||
chr15:41216435 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+233A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216435 | |||||||
chr15:41216466 | T | C | 13 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0063 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.388+202A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216466 | |||||||
chr15:41216587 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+81G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216587 | |||||||
chr15:41216966 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.260+131G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41216966 | |||||||
chr15:41217042 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.260+55T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217042 | |||||||
chr15:41217072 | A | G | 3 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 |
3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.260+25T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217072 | |||||||
chr15:41217090 | T | A | 185 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
splice_region_variant&intron_variant | LOW | c.260+7A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217090 | |||||||
chr15:41217214 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.203-60G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217214 | |||||||
chr15:41217529 | C | CT | 70 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(67): Show |
71 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.203-376dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | |||||||
chr15:41217529 | C | CTT | 7 | a0001c0001t0001g0027 a0001c0001t0002g0140 a0001c0001t0002g0182 others(4): Show |
7 | HG02071.hp2 HG02293.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-377_203-376dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | |||||||
chr15:41217529 | C | CTTT | 71 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(68): Show |
71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.203-378_203-376dup others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | |||||||
chr15:41217529 | C | CTTTT | 9 | a0001c0001t0003g0087 a0001c0001t0004g0077 a0002c0004t0001g0001 others(6): Show |
10 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-379_203-376dup others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | |||||||
chr15:41217597 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-443G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217597 | |||||||
chr15:41217641 | C | G | 1 | a0001c0006t0001g0230 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.203-487G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217641 | |||||||
chr15:41217684 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-530G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217684 | |||||||
chr15:41217748 | C | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-594G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217748 | |||||||
chr15:41217748 | C | G | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.203-594G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217748 | |||||||
chr15:41217828 | C | G | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.203-674G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217828 | |||||||
chr15:41218078 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-924C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218078 | |||||||
chr15:41218142 | C | T | 2 | a0001c0002t0001g0203 a0001c0002t0001g0204 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.203-988G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218142 | |||||||
chr15:41218162 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1008A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218162 | |||||||
chr15:41218197 | C | T | 1 | a0001c0002t0001g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.203-1043G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218197 | |||||||
chr15:41218259 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1105A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218259 | |||||||
chr15:41218296 | A | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1142T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218296 | |||||||
chr15:41218451 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1297G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218451 | |||||||
chr15:41218460 | C | T | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-1306G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218460 | |||||||
chr15:41218486 | C | CA | 64 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0131 others(61): Show |
65 | HG00408.hp1 HG00609.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.203-1333dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | |||||||
chr15:41218486 | C | CAAA | 6 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0004g0005 others(3): Show |
6 | HG02293.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-1335_203-1333d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | |||||||
chr15:41218486 | C | CAAAA | 72 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.203-1336_203-1333d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | |||||||
chr15:41218486 | CA | C | 12 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0001c0002t0001g0227 others(9): Show |
12 | HG01070.hp2 HG01884.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.203-1333delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | |||||||
chr15:41218518 | G | T | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.202+1312C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218518 | |||||||
chr15:41218545 | G | C | 1 | a0002c0003t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202+1285C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218545 | |||||||
chr15:41218561 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+1269T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218561 | |||||||
chr15:41218684 | C | T | 3 | a0001c0002t0001g0304 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | NA18966.hp2 NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.202+1146G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218684 | |||||||
chr15:41218891 | G | A | 1 | a0006c0017t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202+939C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218891 | |||||||
chr15:41218894 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+936A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218894 | |||||||
chr15:41218961 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+869A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218961 | |||||||
chr15:41219061 | C | T | 3 | a0001c0002t0001g0193 a0001c0002t0001g0219 a0001c0002t0001g0220 |
3 | HG00597.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.202+769G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219061 | |||||||
chr15:41219084 | T | C | 1 | a0001c0001t0003g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.202+746A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219084 | |||||||
chr15:41219138 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+692A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219138 | |||||||
chr15:41219151 | C | A | 1 | a0001c0002t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.202+679G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219151 | |||||||
chr15:41219187 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+643T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219187 | |||||||
chr15:41219293 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.202+537T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219293 | |||||||
chr15:41219385 | G | A | 1 | a0001c0002t0001g0213 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.202+445C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219385 | |||||||
chr15:41219607 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+223C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219607 | |||||||
chr15:41219718 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202+112T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219718 | |||||||
chr15:41219751 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+79T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219751 | |||||||
chr15:41219762 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202+68T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219762 | |||||||
chr15:41219819 | G | C | 1 | a0001c0002t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.202+11C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219819 | |||||||
chr15:41220101 | A | C | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.134-203T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220101 | |||||||
chr15:41220187 | T | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-289A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220187 | |||||||
chr15:41220237 | C | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(62): Show |
66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-339G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220237 | |||||||
chr15:41220302 | G | A | 3 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 |
3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.134-404C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220302 | |||||||
chr15:41220339 | C | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-441G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220339 | |||||||
chr15:41220375 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-477T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220375 | |||||||
chr15:41220393 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.134-495G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220393 | |||||||
chr15:41220427 | C | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-529G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220427 | |||||||
chr15:41220474 | T | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-576A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220474 | |||||||
chr15:41220510 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-612T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220510 | |||||||
chr15:41220773 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.134-875A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220773 | |||||||
chr15:41220861 | T | C | 3 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 |
3 | HG00639.hp2 HG00738.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.134-963A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220861 | |||||||
chr15:41221059 | T | C | 185 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.134-1161A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221059 | |||||||
chr15:41221105 | A | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.134-1207T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221105 | |||||||
chr15:41221129 | A | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1231T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221129 | |||||||
chr15:41221154 | T | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1256A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221154 | |||||||
chr15:41221323 | G | C | 1 | a0001c0002t0001g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.134-1425C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221323 | |||||||
chr15:41221330 | G | A | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1432C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221330 | |||||||
chr15:41221419 | G | A | 2 | a0001c0001t0015g0316 a0002c0003t0001g0127 |
2 | HG01070.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.134-1521C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221419 | |||||||
chr15:41221443 | C | CT | 29 | a0001c0002t0001g0193 a0001c0002t0001g0196 a0001c0002t0001g0197 others(26): Show |
29 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-1546dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221443 | |||||||
chr15:41221443 | CT | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1546delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221443 | |||||||
chr15:41221454 | G | A | 2 | a0001c0002t0001g0277 a0001c0002t0001g0294 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.134-1556C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221454 | |||||||
chr15:41221494 | G | A | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.134-1596C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221494 | |||||||
chr15:41221822 | G | C | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1924C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221822 | |||||||
chr15:41221826 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1928T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221826 | |||||||
chr15:41221883 | T | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1985A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221883 | |||||||
chr15:41221935 | AC | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(62): Show |
66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-2038delG | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221935 | |||||||
chr15:41221938 | A | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(62): Show |
66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-2040T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221938 | |||||||
chr15:41221960 | C | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2062G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221960 | |||||||
chr15:41222072 | A | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.134-2174T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222072 | |||||||
chr15:41222100 | G | A | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.134-2202C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222100 | |||||||
chr15:41222136 | C | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2238G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222136 | |||||||
chr15:41222208 | A | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.134-2310T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222208 | |||||||
chr15:41222208 | A | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134-2310T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222208 | |||||||
chr15:41222226 | T | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2328A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222226 | |||||||
chr15:41222273 | G | C | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-2375C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222273 | |||||||
chr15:41222300 | C | A | 4 | a0001c0002t0001g0278 a0001c0002t0001g0279 a0001c0002t0001g0295 others(1): Show |
4 | HG01257.hp1 HG01346.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-2402G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222300 | |||||||
chr15:41222501 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2603T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222501 | |||||||
chr15:41222535 | A | G | 182 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.134-2637T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222535 | |||||||
chr15:41222576 | T | A | 1 | a0002c0003t0010g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.134-2678A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222576 | |||||||
chr15:41222600 | A | G | 4 | a0002c0003t0005g0098 a0002c0003t0005g0099 a0002c0003t0005g0100 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-2702T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222600 | |||||||
chr15:41222638 | A | AT | 11 | a0001c0001t0002g0089 a0001c0001t0002g0137 a0001c0002t0001g0212 others(8): Show |
11 | HG00609.hp2 HG02027.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-2741dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | |||||||
chr15:41222638 | AT | A | 35 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 others(32): Show |
35 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.134-2741delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | |||||||
chr15:41222638 | ATTTT | A | 72 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-2744_134-2741d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | |||||||
chr15:41222638 | ATTTTT | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-2745_134-2741d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | |||||||
chr15:41222643 | T | A | 1 | a0001c0001t0004g0076 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-2745A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222643 | |||||||
chr15:41222665 | G | A | 3 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 |
3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.134-2767C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222665 | |||||||
chr15:41222678 | G | C | 182 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.134-2780C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222678 | |||||||
chr15:41222712 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2814T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222712 | |||||||
chr15:41222763 | C | T | 1 | a0001c0002t0009g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.134-2865G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222763 | |||||||
chr15:41222773 | A | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2875T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222773 | |||||||
chr15:41222774 | T | TA | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2877dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222774 | |||||||
chr15:41222934 | C | CA | 27 | a0001c0002t0001g0113 a0001c0002t0001g0193 a0001c0002t0001g0200 others(24): Show |
27 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.134-3037dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | |||||||
chr15:41222934 | CA | C | 45 | a0001c0001t0015g0316 a0001c0002t0001g0201 a0001c0002t0001g0202 others(42): Show |
45 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.134-3037delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | |||||||
chr15:41222934 | CAAAAAAA others(1): Show |
C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0002 others(131): Show |
136 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.134-3044_134-3037d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | |||||||
chr15:41222934 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02109.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-3045_134-3037d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | |||||||
chr15:41223005 | C | T | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-3107G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223005 | |||||||
chr15:41223016 | T | G | 66 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.134-3118A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223016 | |||||||
chr15:41223391 | G | C | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.133+3052C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223391 | |||||||
chr15:41223738 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.133+2705C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223738 | |||||||
chr15:41223761 | A | G | 1 | a0001c0002t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133+2682T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223761 | |||||||
chr15:41223789 | C | T | 5 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(2): Show |
5 | HG01192.hp1 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+2654G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223789 | |||||||
chr15:41223807 | G | A | 1 | a0001c0002t0001g0296 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.133+2636C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223807 | |||||||
chr15:41223822 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2621T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223822 | |||||||
chr15:41223932 | C | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(62): Show |
66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.133+2511G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223932 | |||||||
chr15:41223999 | T | C | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2444A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223999 | |||||||
chr15:41224083 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133+2360C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224083 | |||||||
chr15:41224092 | A | C | 1 | a0005c0009t0001g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.133+2351T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224092 | |||||||
chr15:41224230 | G | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(62): Show |
66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.133+2213C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224230 | |||||||
chr15:41224280 | T | C | 3 | a0003c0007t0003g0078 a0003c0007t0003g0079 a0003c0007t0003g0080 |
3 | NA18968.hp1 NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.133+2163A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224280 | |||||||
chr15:41224362 | C | T | 4 | a0002c0003t0005g0098 a0002c0003t0005g0099 a0002c0003t0005g0100 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+2081G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224362 | |||||||
chr15:41224415 | T | C | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2028A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224415 | |||||||
chr15:41224473 | C | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1970G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224473 | |||||||
chr15:41224487 | A | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+1956T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224487 | |||||||
chr15:41224625 | C | T | 29 | a0001c0005t0001g0107 a0002c0003t0001g0010 a0002c0003t0001g0102 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.133+1818G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224625 | |||||||
chr15:41224650 | G | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.133+1793C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224650 | |||||||
chr15:41224674 | C | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1769G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224674 | |||||||
chr15:41224782 | C | T | 1 | a0002c0003t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.133+1661G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224782 | |||||||
chr15:41224899 | G | C | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.133+1544C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224899 | |||||||
chr15:41224967 | T | TA | 149 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(146): Show |
151 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.133+1475dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224967 | |||||||
chr15:41225093 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1350T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225093 | |||||||
chr15:41225288 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133+1155A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225288 | |||||||
chr15:41225303 | G | A | 1 | a0001c0002t0001g0298 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.133+1140C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225303 | |||||||
chr15:41225320 | C | T | 3 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 |
3 | NA18942.hp2 NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.133+1123G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225320 | |||||||
chr15:41225334 | C | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1109G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225334 | |||||||
chr15:41225348 | G | GCCAAGGT others(41): Show |
1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.133+1047_133+1094d others(50): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225348 | |||||||
chr15:41225429 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1014T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225429 | |||||||
chr15:41225483 | G | C | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+960C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225483 | |||||||
chr15:41225587 | G | GA | 14 | a0002c0003t0001g0115 a0002c0003t0001g0116 a0002c0003t0001g0117 others(11): Show |
14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+855dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | |||||||
chr15:41225587 | GA | G | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.133+855delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | |||||||
chr15:41225587 | GAA | G | 5 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+854_133+855del others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | |||||||
chr15:41225706 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.133+737C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225706 | |||||||
chr15:41225749 | A | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+694T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225749 | |||||||
chr15:41225774 | G | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.133+669C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225774 | |||||||
chr15:41225822 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+621T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225822 | |||||||
chr15:41225901 | CAAAACAA others(4): Show |
C | 72 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.133+531_133+541del others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225901 | |||||||
chr15:41225911 | C | CA | 5 | a0001c0002t0001g0193 a0001c0002t0001g0288 a0001c0002t0001g0293 others(2): Show |
5 | HG00597.hp2 HG03098.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+531dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225911 | |||||||
chr15:41225919 | AC | A | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
77 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.133+523delG | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225919 | |||||||
chr15:41225920 | C | A | 72 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.133+523G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225920 | |||||||
chr15:41225974 | T | C | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+469A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225974 | |||||||
chr15:41225975 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0089 a0001c0001t0002g0130 others(60): Show |
64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.133+468G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225975 | |||||||
chr15:41226019 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+424T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226019 | |||||||
chr15:41226024 | A | G | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+419T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226024 | |||||||
chr15:41226045 | G | C | 1 | a0002c0003t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.133+398C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226045 | |||||||
chr15:41226079 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.133+364A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226079 | |||||||
chr15:41226177 | G | A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0008 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133+266C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226177 | |||||||
chr15:41226184 | A | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.133+259T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226184 | |||||||
chr15:41226720 | T | G | 1 | a0001c0001t0003g0082 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-53-92A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226720 | |||||||
chr15:41226734 | T | C | 2 | a0001c0002t0001g0302 a0001c0002t0001g0303 |
2 | NA18971.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-53-106A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226734 | |||||||
chr15:41226991 | G | T | 3 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 |
3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-53-363C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226991 | |||||||
chr15:41227115 | T | G | 7 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0083 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-487A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227115 | |||||||
chr15:41227182 | C | A | 9 | a0001c0002t0001g0128 a0001c0002t0001g0304 a0001c0002t0001g0305 others(6): Show |
9 | HG01943.hp1 HG01952.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-554G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227182 | |||||||
chr15:41227427 | T | C | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-53-799A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227427 | |||||||
chr15:41227498 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-53-870A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227498 | |||||||
chr15:41227539 | T | C | 152 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(149): Show |
154 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.-53-911A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227539 | |||||||
chr15:41227619 | G | A | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-991C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227619 | |||||||
chr15:41227635 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-53-1007C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227635 | |||||||
chr15:41227675 | CAA | C | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
145 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.-53-1049_-53-1048d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227675 | |||||||
chr15:41227861 | C | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1233G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227861 | |||||||
chr15:41227862 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1234G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227862 | |||||||
chr15:41227866 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1238T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227866 | |||||||
chr15:41227868 | G | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1240C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227868 | |||||||
chr15:41227871 | GAAACCCC others(22): Show |
G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1272_-53-1244d others(31): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227871 | |||||||
chr15:41227878 | C | T | 1 | a0002c0003t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-53-1250G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227878 | |||||||
chr15:41227902 | T | TTGTGGGG others(3): Show |
1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1275_-53-1274i others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227902 | |||||||
chr15:41227903 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1275T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227903 | |||||||
chr15:41227905 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1277G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227905 | |||||||
chr15:41227906 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1278G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227906 | |||||||
chr15:41227907 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1279T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227907 | |||||||
chr15:41227909 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1281G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227909 | |||||||
chr15:41227910 | T | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1282A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227910 | |||||||
chr15:41227913 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1285T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227913 | |||||||
chr15:41227916 | G | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1288C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227916 | |||||||
chr15:41227917 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1289T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227917 | |||||||
chr15:41227918 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1290G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227918 | |||||||
chr15:41227975 | A | G | 2 | a0001c0002t0014g0094 a0004c0014t0001g0194 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-53-1347T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227975 | |||||||
chr15:41228116 | T | G | 1 | a0001c0002t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-53-1488A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228116 | |||||||
chr15:41228125 | A | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1497T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228125 | |||||||
chr15:41228221 | C | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1593G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228221 | |||||||
chr15:41228317 | T | C | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-1689A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228317 | |||||||
chr15:41228334 | G | A | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1706C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228334 | |||||||
chr15:41228450 | G | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1822C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228450 | |||||||
chr15:41228609 | C | A | 4 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0189 others(1): Show |
4 | NA19005.hp1 NA19055.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+1870G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228609 | |||||||
chr15:41228637 | G | A | 72 | a0001c0001t0001g0027 a0001c0001t0003g0011 a0001c0001t0003g0026 others(69): Show |
73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-54+1842C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228637 | |||||||
chr15:41228732 | C | T | 4 | a0002c0003t0001g0009 a0002c0003t0001g0091 a0002c0003t0001g0092 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+1747G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228732 | |||||||
chr15:41228754 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-54+1725T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228754 | |||||||
chr15:41228787 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-54+1692G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228787 | |||||||
chr15:41228830 | A | G | 1 | a0001c0001t0004g0012 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-54+1649T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228830 | |||||||
chr15:41229139 | C | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+1340G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229139 | |||||||
chr15:41229206 | G | A | 1 | a0002c0004t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+1273C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229206 | |||||||
chr15:41229218 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-54+1261G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229218 | |||||||
chr15:41229284 | CCTAGACA others(21): Show |
C | 1 | a0001c0001t0002g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-54+1167_-54+1194d others(30): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229284 | |||||||
chr15:41229295 | T | A | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-54+1184A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229295 | |||||||
chr15:41229384 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1095T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229384 | |||||||
chr15:41229391 | T | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1088A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229391 | |||||||
chr15:41229407 | GGAGGTTG others(19): Show |
G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1046_-54+1071d others(28): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229407 | |||||||
chr15:41229539 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-54+940G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229539 | |||||||
chr15:41229636 | C | T | 148 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+843G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229636 | |||||||
chr15:41229769 | A | AAACAAC | 83 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-54+704_-54+709dup others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229769 | |||||||
chr15:41229787 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-54+692G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229787 | |||||||
chr15:41229921 | G | A | 1 | a0002c0004t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+558C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229921 | |||||||
chr15:41230082 | C | CT | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-54+396dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230082 | |||||||
chr15:41230082 | C | CTT | 6 | a0001c0001t0004g0005 a0001c0005t0001g0007 a0001c0005t0001g0008 others(3): Show |
6 | HG01109.hp1 HG02074.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+395_-54+396dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230082 | |||||||
chr15:41230091 | T | C | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+388A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230091 |