Item | Value |
---|---|
geneid | 26060 |
ensemblid | ENSG00000157500.12 |
hgncid | 24035 |
symbol | APPL1 |
name | adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 |
refseq_nuc | NM_012096.3 |
refseq_prot | NP_036228.1 |
ensembl_nuc | ENST00000288266.8 |
ensembl_prot | ENSP00000288266.3 |
mane_status | MANE Select |
chr | chr3 |
start | 57227729 |
end | 57273471 |
strand | + |
ver | v1.2 |
region | chr3:57227729-57273471 |
region5000 | chr3:57222729-57278471 |
regionname0 | APPL1_chr3_57227729_57273471 |
regionname5000 | APPL1_chr3_57222729_57278471 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 709 | 235 | 81 | 47 | 60 | 11 | 35 | 48 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0002 | 0/1 | 709 | 20 | 0 | 11 | 0 | 3 | 5 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0003 | 0/0 | 709 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0004 | 0/0 | 709 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0005 | 0/0 | 709 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0006 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
a0007 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | MPGID others(704): Show |
chr3 | 57222729 | 57278471 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2127 | 227 | 77 | 44 | 60 | 11 | 34 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0001c0004 | 0/0 | 2127 | 5 | 4 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0001c0006 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0001c0009 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0001c0011 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0002c0002 | 0/1 | 2127 | 20 | 0 | 11 | 0 | 3 | 5 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0003c0003 | 0/0 | 2127 | 6 | 6 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0004c0005 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0005c0010 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0006c0007 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 | ||
a0007c0008 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | ATGCC others(2122): Show |
chr3 | 57222729 | 57278471 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6069 | 90 | 6 | 19 | 41 | 7 | 17 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0002 | 1/0 | 6069 | 62 | 8 | 16 | 18 | 4 | 15 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0003 | 0/0 | 6067 | 21 | 19 | 2 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6062): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0004 | 0/0 | 6069 | 18 | 16 | 2 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0005 | 0/0 | 6069 | 6 | 6 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0006 | 0/0 | 6069 | 4 | 4 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0007 | 0/0 | 6070 | 3 | 3 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6065): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0008 | 0/0 | 6068 | 3 | 3 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6063): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0010 | 0/0 | 6069 | 3 | 2 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0011 | 0/0 | 6069 | 2 | 0 | 2 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0012 | 0/0 | 6069 | 2 | 0 | 1 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0014 | 0/0 | 6069 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0015 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0016 | 0/0 | 6068 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6063): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0017 | 0/0 | 6047 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6042): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0018 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6065): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0019 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0020 | 0/0 | 6069 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0021 | 0/0 | 6067 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6062): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0022 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0023 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0024 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0001t0025 | 0/0 | 6069 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0004t0009 | 0/0 | 6070 | 3 | 2 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6065): Show |
chr3 | 57222729 | 57278471 |
a0001c0004t0013 | 0/0 | 6070 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6065): Show |
chr3 | 57222729 | 57278471 |
a0001c0006t0002 | 0/0 | 6069 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0009t0002 | 0/0 | 6069 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0001c0011t0002 | 0/0 | 6069 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0002c0002t0003 | 0/1 | 6067 | 20 | 0 | 11 | 0 | 3 | 5 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6062): Show |
chr3 | 57222729 | 57278471 |
a0003c0003t0004 | 0/0 | 6069 | 6 | 6 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0004c0005t0001 | 0/0 | 6069 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0005c0010t0004 | 0/0 | 6069 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0006c0007t0002 | 0/0 | 6069 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
a0007c0008t0001 | 0/0 | 6069 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | GCACG others(6064): Show |
chr3 | 57222729 | 57278471 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 1 | 0 | 6 | 2 | 2 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0010g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0011g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0011g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0012g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0016g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0017g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0019g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0020g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0021g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0022g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0023g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0024g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0001t0025g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0004t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0004t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0004t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0004t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0004t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0006t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0009t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0001c0011t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0003c0003t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0004c0005t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0005c0010t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0006c0007t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
a0007c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0004 | EUR | FIN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0089 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0158 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01081 | hp2 | a0001 | c0011 | t0002 | g0129 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01099 | hp1 | a0002 | c0002 | t0003 | g0108 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01109 | hp1 | a0001 | c0004 | t0009 | g0153 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01256 | hp1 | a0002 | c0002 | t0003 | g0122 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01257 | hp1 | a0001 | c0001 | t0011 | g0014 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01258 | hp1 | a0001 | c0001 | t0011 | g0015 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01358 | hp1 | a0001 | c0009 | t0002 | g0098 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0106 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01433 | hp2 | a0002 | c0002 | t0003 | g0092 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01496 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0023 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0138 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0023 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0091 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01934 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01993 | hp1 | a0002 | c0002 | t0003 | g0096 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0103 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02451 | hp1 | a0001 | c0004 | t0013 | g0155 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0191 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02630 | hp1 | a0005 | c0010 | t0004 | g0186 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0121 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02717 | hp1 | a0001 | c0004 | t0009 | g0180 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02809 | hp2 | a0003 | c0003 | t0004 | g0190 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02886 | hp1 | a0003 | c0003 | t0004 | g0187 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0030 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02922 | hp1 | a0003 | c0003 | t0004 | g0188 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02965 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02976 | hp1 | a0001 | c0004 | t0009 | g0154 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03130 | hp2 | a0001 | c0001 | t0022 | g0192 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03139 | hp2 | a0001 | c0001 | t0021 | g0026 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0005 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03453 | hp1 | a0001 | c0001 | t0023 | g0184 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0182 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03579 | hp2 | a0001 | c0004 | t0013 | g0152 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0033 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03669 | hp2 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0005 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03927 | hp2 | a0001 | c0006 | t0002 | g0117 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04204 | hp1 | a0001 | c0001 | t0017 | g0161 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | STU | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0116 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18946 | hp1 | a0001 | c0001 | t0025 | g0055 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18982 | hp2 | a0006 | c0007 | t0002 | g0194 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19030 | hp1 | a0001 | c0001 | t0018 | g0102 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19090 | hp2 | a0007 | c0008 | t0001 | g0086 | EAS | JPT | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | YRI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20129 | hp1 | a0003 | c0003 | t0004 | g0181 | AFR | ASW | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ASW | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0137 | EUR | TSI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | TSI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20905 | hp1 | a0002 | c0002 | t0003 | g0104 | SAS | GIH | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG01123 | hp2 | a0001 | c0001 | t0020 | g0037 | AMR | CLM | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0183 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0185 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0088 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02559 | hp1 | a0001 | c0001 | t0024 | g0189 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG02559 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | ACB | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0156 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0120 | AFR | USA | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | USA | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0099 | REF | REF | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0025 | REF | REF | APPL1_chr3_57222729_57278471 | APPL1 | chr3 | 57222729 | 57278471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57237538 | A | G | 1 | a0005 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.200A>G | p.Glu67Gly | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 3/22 | 355/6069 | 200/2130 | 67/709 | chr3 | 57237538 | |||
chr3:57242121 | G | A | 1 | a0006 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.394G>A | p.Val132Ile | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 6/22 | 549/6069 | 394/2130 | 132/709 | chr3 | 57242121 | |||
chr3:57249498 | C | G | 1 | a0003 | 6 | HG02109.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
missense_variant | MODERATE | c.1002C>G | p.Asp334Glu | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/22 | 1157/6069 | 1002/2130 | 334/709 | chr3 | 57249498 | |||
chr3:57257260 | C | T | 1 | a0004 | 2 | HG02559.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.1262C>T | p.Pro421Leu | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/22 | 1417/6069 | 1262/2130 | 421/709 | chr3 | 57257260 | |||
chr3:57268430 | A | G | 1 | a0007 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1926A>G | p.Ile642Met | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/22 | 2081/6069 | 1926/2130 | 642/709 | chr3 | 57268430 | |||
chr3:57269656 | A | G | 1 | a0002 | 19 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(16): Show |
missense_variant | MODERATE | c.2099A>G | p.Glu700Gly | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2254/6069 | 2099/2130 | 700/709 | chr3 | 57269656 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57227892 | G | A | 1 | a0001c0006 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.9G>A | p.Gly3Gly | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | 164/6069 | 9/2130 | 3/709 | chr3 | 57227892 | |||
chr3:57235580 | A | G | 1 | a0001c0011 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.69A>G | p.Leu23Leu | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/22 | 224/6069 | 69/2130 | 23/709 | chr3 | 57235580 | |||
chr3:57248238 | A | G | 1 | a0001c0009 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.750A>G | p.Thr250Thr | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 10/22 | 905/6069 | 750/2130 | 250/709 | chr3 | 57248238 | |||
chr3:57257010 | A | G | 1 | a0001c0004 | 5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.1206A>G | p.Pro402Pro | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 14/22 | 1361/6069 | 1206/2130 | 402/709 | chr3 | 57257010 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57227744 | G | C | 1 | a0001c0001t0015 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | 140 | chr3 | 57227744 | ||||||
chr3:57227762 | G | T | 1 | a0001c0001t0025 | 1 | NA18946.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-122G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | chr3 | 57227762 | |||||||
chr3:57227798 | G | A | 1 | a0001c0001t0011 | 2 | HG01257.hp1 HG01258.hp1 |
5_prime_UTR_variant | MODIFIER | c.-86G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | 86 | chr3 | 57227798 | ||||||
chr3:57227856 | C | T | 1 | a0001c0001t0024 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-28C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | 28 | chr3 | 57227856 | ||||||
chr3:57227866 | C | T | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(6): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/22 | chr3 | 57227866 | |||||||
chr3:57270189 | T | G | 2 | a0001c0001t0010 a0001c0001t0022 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*502T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 502 | chr3 | 57270189 | ||||||
chr3:57270199 | T | C | 1 | a0001c0001t0024 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 512 | chr3 | 57270199 | ||||||
chr3:57270522 | A | G | 2 | a0001c0001t0005 a0001c0001t0006 |
10 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*835A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 835 | chr3 | 57270522 | ||||||
chr3:57270581 | G | A | 1 | a0001c0001t0007 | 3 | HG01884.hp1 HG02922.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*894G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 894 | chr3 | 57270581 | ||||||
chr3:57270961 | G | A | 1 | a0001c0001t0015 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1274G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1274 | chr3 | 57270961 | ||||||
chr3:57270977 | C | T | 1 | a0001c0001t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1290 | chr3 | 57270977 | ||||||
chr3:57271142 | C | T | 3 | a0001c0001t0003 a0001c0001t0021 a0002c0002t0003 |
41 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1455C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1455 | chr3 | 57271142 | ||||||
chr3:57271215 | A | G | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*1528A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1528 | chr3 | 57271215 | ||||||
chr3:57271222 | TCA | T | 3 | a0001c0001t0003 a0001c0001t0021 a0002c0002t0003 |
41 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1539_*1540delAC | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1539 | INFO_REALIGN_3_PRIME | chr3 | 57271222 | |||||
chr3:57271446 | T | C | 1 | a0001c0001t0021 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 1759 | chr3 | 57271446 | ||||||
chr3:57271759 | G | T | 1 | a0001c0001t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2072G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2072 | chr3 | 57271759 | ||||||
chr3:57271821 | C | T | 1 | a0001c0001t0020 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2134C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2134 | chr3 | 57271821 | ||||||
chr3:57271843 | T | C | 1 | a0001c0001t0012 | 2 | HG00639.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2156T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2156 | chr3 | 57271843 | ||||||
chr3:57271890 | TC | T | 2 | a0001c0001t0008 a0001c0001t0016 |
4 | HG02280.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2205delC | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2205 | INFO_REALIGN_3_PRIME | chr3 | 57271890 | |||||
chr3:57272101 | T | C | 2 | a0001c0004t0009 a0001c0004t0013 |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2414T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2414 | chr3 | 57272101 | ||||||
chr3:57272155 | T | C | 1 | a0001c0001t0010 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2468T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2468 | chr3 | 57272155 | ||||||
chr3:57272198 | C | T | 1 | a0001c0001t0016 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2511C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2511 | chr3 | 57272198 | ||||||
chr3:57272291 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*2604T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2604 | chr3 | 57272291 | ||||||
chr3:57272583 | C | A | 3 | a0001c0001t0003 a0001c0001t0021 a0002c0002t0003 |
41 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2896C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2896 | chr3 | 57272583 | ||||||
chr3:57272598 | G | GA | 2 | a0001c0004t0009 a0001c0004t0013 |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2920dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2921 | INFO_REALIGN_3_PRIME | chr3 | 57272598 | |||||
chr3:57272610 | G | GT | 2 | a0001c0001t0007 a0001c0001t0018 |
4 | HG01884.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2930dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 2931 | INFO_REALIGN_3_PRIME | chr3 | 57272610 | |||||
chr3:57272754 | C | T | 6 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0020 others(3): Show |
97 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3067C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3067 | chr3 | 57272754 | ||||||
chr3:57272850 | C | T | 1 | a0001c0004t0009 | 3 | HG01109.hp1 HG02717.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3163C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3163 | chr3 | 57272850 | ||||||
chr3:57272909 | A | G | 1 | a0001c0001t0014 | 2 | HG02486.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3222A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3222 | chr3 | 57272909 | ||||||
chr3:57272933 | G | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*3246G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3246 | chr3 | 57272933 | ||||||
chr3:57273243 | TAATCATG others(15): Show |
T | 1 | a0001c0001t0017 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3566_*3587delGTGT others(18): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3566 | INFO_REALIGN_3_PRIME | chr3 | 57273243 | |||||
chr3:57273263 | C | T | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
41 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3576C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 22/22 | 3576 | chr3 | 57273263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57228000 | C | T | 16 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(13): Show |
22 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+63C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57228000 | |||||||
chr3:57228132 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0002g0006 a0001c0001t0002g0193 others(1): Show |
6 | NA18946.hp2 NA18950.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+195C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57228132 | |||||||
chr3:57228186 | G | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.54+249G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57228186 | |||||||
chr3:57228627 | G | T | 16 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(13): Show |
22 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+690G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57228627 | |||||||
chr3:57228798 | T | C | 1 | a0001c0001t0012g0033 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.54+861T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57228798 | |||||||
chr3:57229184 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.54+1247G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57229184 | |||||||
chr3:57229366 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
96 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.54+1429G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57229366 | |||||||
chr3:57229394 | A | G | 1 | a0007c0008t0001g0086 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.54+1457A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57229394 | |||||||
chr3:57229433 | C | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+1496C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57229433 | |||||||
chr3:57229699 | C | CT | 49 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0034 others(46): Show |
53 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.54+1790dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57229699 | ||||||
chr3:57229699 | C | CTT | 8 | a0001c0001t0001g0085 a0001c0001t0014g0182 a0001c0001t0014g0185 others(5): Show |
8 | HG01433.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1789_54+1790dup others(2): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57229699 | ||||||
chr3:57229699 | C | CTTT | 10 | a0001c0001t0004g0012 a0001c0001t0004g0032 a0001c0001t0004g0196 others(7): Show |
13 | HG01167.hp2 HG01169.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+1788_54+1790dup others(3): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57229699 | ||||||
chr3:57229699 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0004g0011 a0001c0001t0004g0031 a0001c0001t0004g0197 others(2): Show |
8 | HG01891.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+1778_54+1790del others(13): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57229699 | ||||||
chr3:57229724 | T | G | 2 | a0001c0001t0002g0087 a0001c0001t0019g0088 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.54+1787T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57229724 | |||||||
chr3:57230041 | A | C | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+2104A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230041 | |||||||
chr3:57230229 | CT | C | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+2295delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57230229 | ||||||
chr3:57230314 | C | G | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+2377C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230314 | |||||||
chr3:57230742 | G | A | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+2805G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230742 | |||||||
chr3:57230844 | T | A | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+2907T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230844 | |||||||
chr3:57230844 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(73): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.54+2907T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230844 | |||||||
chr3:57230853 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.54+2916A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230853 | |||||||
chr3:57230880 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.54+2943C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230880 | |||||||
chr3:57230992 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.54+3055G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57230992 | |||||||
chr3:57231000 | T | C | 1 | a0001c0001t0006g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.54+3063T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231000 | |||||||
chr3:57231103 | G | A | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+3166G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231103 | |||||||
chr3:57231199 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.54+3262C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231199 | |||||||
chr3:57231287 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0179 |
2 | HG01257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.54+3350C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231287 | |||||||
chr3:57231312 | C | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0031 a0001c0001t0004g0197 others(2): Show |
8 | HG01891.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+3375C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231312 | |||||||
chr3:57231338 | C | CA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
92 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.54+3422dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57231338 | ||||||
chr3:57231338 | C | CAA | 4 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
5 | HG01884.hp1 HG03927.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+3421_54+3422dup others(2): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57231338 | ||||||
chr3:57231338 | CA | C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0175 a0001c0001t0002g0006 others(52): Show |
60 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.54+3422delA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57231338 | ||||||
chr3:57231359 | A | G | 28 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(25): Show |
35 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.54+3422A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231359 | |||||||
chr3:57231360 | G | A | 28 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(25): Show |
35 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.54+3423G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231360 | |||||||
chr3:57231364 | A | T | 27 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(24): Show |
34 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.54+3427A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231364 | |||||||
chr3:57231553 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0082 |
2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.54+3616A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231553 | |||||||
chr3:57231750 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.54+3813G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231750 | |||||||
chr3:57231752 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0083 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.55-3814G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231752 | |||||||
chr3:57231809 | T | TA | 18 | a0001c0001t0001g0068 a0001c0001t0004g0011 a0001c0001t0004g0012 others(15): Show |
24 | HG00639.hp1 HG01123.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-3740dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57231809 | ||||||
chr3:57231809 | TA | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0150 others(5): Show |
8 | HG01243.hp2 HG01256.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-3740delA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57231809 | ||||||
chr3:57231891 | G | A | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-3675G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231891 | |||||||
chr3:57231897 | A | G | 16 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(13): Show |
22 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-3669A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57231897 | |||||||
chr3:57232044 | T | C | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.55-3522T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232044 | |||||||
chr3:57232159 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.55-3407G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232159 | |||||||
chr3:57232276 | C | G | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.55-3290C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232276 | |||||||
chr3:57232309 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.55-3257G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232309 | |||||||
chr3:57232352 | A | G | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.55-3214A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232352 | |||||||
chr3:57232416 | T | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0069 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-3150T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232416 | |||||||
chr3:57232447 | A | T | 1 | a0001c0001t0002g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-3119A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232447 | |||||||
chr3:57232666 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.55-2900T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232666 | |||||||
chr3:57232745 | G | A | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55-2821G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232745 | |||||||
chr3:57232805 | A | G | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.55-2761A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232805 | |||||||
chr3:57232939 | G | A | 2 | a0001c0001t0008g0113 a0001c0001t0008g0114 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.55-2627G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232939 | |||||||
chr3:57232981 | G | A | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-2585G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57232981 | |||||||
chr3:57233480 | T | C | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.55-2086T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57233480 | |||||||
chr3:57233540 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.55-2026C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57233540 | |||||||
chr3:57233678 | G | T | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-1888G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57233678 | |||||||
chr3:57233838 | T | A | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.55-1728T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57233838 | |||||||
chr3:57233980 | A | G | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.55-1586A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57233980 | |||||||
chr3:57234296 | C | CT | 12 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0069 others(9): Show |
12 | HG00639.hp1 HG01109.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.55-1251dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57234296 | ||||||
chr3:57234296 | C | CTT | 19 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(16): Show |
26 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.55-1252_55-1251dup others(2): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57234296 | ||||||
chr3:57234296 | C | CTTT | 10 | a0001c0001t0004g0199 a0001c0001t0004g0201 a0001c0001t0014g0182 others(7): Show |
10 | HG02109.hp2 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-1253_55-1251dup others(3): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57234296 | ||||||
chr3:57234320 | C | T | 4 | a0001c0001t0008g0113 a0001c0001t0008g0114 a0001c0001t0008g0121 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1246C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234320 | |||||||
chr3:57234353 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
135 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.55-1213G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234353 | |||||||
chr3:57234379 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.55-1187G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234379 | |||||||
chr3:57234446 | C | G | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-1120C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234446 | |||||||
chr3:57234472 | G | A | 1 | a0007c0008t0001g0086 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.55-1094G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234472 | |||||||
chr3:57234587 | C | T | 1 | a0005c0010t0004g0186 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.55-979C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234587 | |||||||
chr3:57234690 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.55-876C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234690 | |||||||
chr3:57234718 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0070 |
2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.55-848T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234718 | |||||||
chr3:57234854 | A | T | 1 | a0001c0004t0013g0155 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.55-712A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234854 | |||||||
chr3:57234951 | G | A | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.55-615G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57234951 | |||||||
chr3:57235300 | G | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.55-266G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | chr3 | 57235300 | |||||||
chr3:57235441 | ATAGAT | A | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-122_55-118delGA others(3): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 57235441 | ||||||
chr3:57235778 | T | A | 1 | a0002c0002t0003g0096 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.153+114T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57235778 | |||||||
chr3:57235825 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.153+161A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57235825 | |||||||
chr3:57236044 | C | CT | 46 | a0001c0001t0001g0006 a0001c0001t0001g0175 a0001c0001t0002g0006 others(43): Show |
51 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.153+397dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 57236044 | ||||||
chr3:57236044 | CT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(98): Show |
135 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.153+397delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 57236044 | ||||||
chr3:57236176 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153+512C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236176 | |||||||
chr3:57236185 | C | T | 1 | a0001c0001t0014g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.153+521C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236185 | |||||||
chr3:57236271 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0083 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+607C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236271 | |||||||
chr3:57236330 | CT | C | 6 | a0001c0001t0003g0097 a0001c0004t0009g0153 a0001c0004t0009g0154 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+680delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 57236330 | ||||||
chr3:57236331 | T | C | 1 | a0001c0001t0012g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.153+667T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236331 | |||||||
chr3:57236350 | T | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.153+686T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236350 | |||||||
chr3:57236393 | A | G | 2 | a0001c0001t0003g0093 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.153+729A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236393 | |||||||
chr3:57236399 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0004c0005t0001g0020 |
4 | HG02559.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+735G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236399 | |||||||
chr3:57236438 | T | C | 22 | a0001c0001t0002g0027 a0001c0001t0002g0109 a0001c0001t0002g0127 others(19): Show |
23 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.153+774T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236438 | |||||||
chr3:57236490 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
140 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.153+826A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236490 | |||||||
chr3:57236575 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.153+911G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236575 | |||||||
chr3:57236853 | C | T | 1 | a0002c0002t0003g0108 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.154-639C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236853 | |||||||
chr3:57236985 | C | A | 1 | a0001c0001t0002g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.154-507C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57236985 | |||||||
chr3:57237179 | C | T | 1 | a0003c0003t0004g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-313C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 2/21 | chr3 | 57237179 | |||||||
chr3:57237885 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0004c0005t0001g0020 |
4 | HG02559.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-160G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 3/21 | chr3 | 57237885 | |||||||
chr3:57238122 | C | T | 16 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(13): Show |
22 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.285+6C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238122 | |||||||
chr3:57238331 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0091 |
3 | HG01884.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.285+215C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238331 | |||||||
chr3:57238369 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.285+253T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238369 | |||||||
chr3:57238409 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.285+293A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238409 | |||||||
chr3:57238421 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+305T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238421 | |||||||
chr3:57238735 | C | T | 1 | a0001c0004t0009g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+619C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238735 | |||||||
chr3:57238809 | A | G | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.285+693A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238809 | |||||||
chr3:57238911 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.285+795G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238911 | |||||||
chr3:57238931 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.285+815G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57238931 | |||||||
chr3:57239039 | G | A | 2 | a0001c0001t0010g0030 a0001c0001t0010g0191 |
3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.285+923G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239039 | |||||||
chr3:57239076 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285+960G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239076 | |||||||
chr3:57239077 | A | G | 1 | a0001c0001t0004g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285+961A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239077 | |||||||
chr3:57239102 | G | A | 1 | a0001c0011t0002g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.285+986G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239102 | |||||||
chr3:57239107 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.285+991T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239107 | |||||||
chr3:57239200 | G | A | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.285+1084G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239200 | |||||||
chr3:57239278 | C | T | 15 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0026 others(12): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.285+1162C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239278 | |||||||
chr3:57239494 | G | A | 2 | a0001c0001t0004g0012 a0001c0001t0004g0203 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-971G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239494 | |||||||
chr3:57239783 | C | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-682C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239783 | |||||||
chr3:57239897 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.286-568G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57239897 | |||||||
chr3:57240026 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.286-439C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57240026 | |||||||
chr3:57240100 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-365A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | chr3 | 57240100 | |||||||
chr3:57240131 | G | GT | 28 | a0001c0001t0002g0112 a0001c0001t0002g0172 a0001c0001t0003g0002 others(25): Show |
40 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.286-320dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 57240131 | ||||||
chr3:57240719 | T | C | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373+167T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 5/21 | chr3 | 57240719 | |||||||
chr3:57240798 | ACACTTAT others(2): Show |
A | 1 | a0001c0001t0005g0010 | 3 | HG02258.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.373+248_373+256del others(9): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 57240798 | ||||||
chr3:57241117 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
140 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.373+565A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 5/21 | chr3 | 57241117 | |||||||
chr3:57241293 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.373+741T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 5/21 | chr3 | 57241293 | |||||||
chr3:57241930 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.374-171T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 5/21 | chr3 | 57241930 | |||||||
chr3:57242230 | GA | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.415+96delA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 57242230 | ||||||
chr3:57242662 | A | G | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-194A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 6/21 | chr3 | 57242662 | |||||||
chr3:57242799 | C | A | 1 | a0001c0001t0015g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.416-57C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 6/21 | chr3 | 57242799 | |||||||
chr3:57243018 | T | A | 1 | a0001c0001t0017g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.474+104T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243018 | |||||||
chr3:57243096 | A | G | 3 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 |
3 | HG01109.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.474+182A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243096 | |||||||
chr3:57243207 | C | T | 2 | a0001c0001t0024g0189 a0005c0010t0004g0186 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.474+293C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243207 | |||||||
chr3:57243246 | T | C | 1 | a0002c0002t0003g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.474+332T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243246 | |||||||
chr3:57243801 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.474+887A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243801 | |||||||
chr3:57243895 | C | T | 4 | a0001c0001t0002g0157 a0001c0001t0007g0022 a0001c0001t0007g0091 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+981C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243895 | |||||||
chr3:57243928 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.474+1014A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57243928 | |||||||
chr3:57244296 | C | G | 5 | a0001c0001t0004g0011 a0001c0001t0004g0031 a0001c0001t0004g0197 others(2): Show |
8 | HG01891.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+1382C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244296 | |||||||
chr3:57244421 | G | T | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.474+1507G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244421 | |||||||
chr3:57244635 | T | A | 5 | a0003c0003t0004g0181 a0003c0003t0004g0183 a0003c0003t0004g0187 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-1441T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244635 | |||||||
chr3:57244635 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
6 | HG01934.hp2 HG02040.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-1441T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244635 | |||||||
chr3:57244645 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
146 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.475-1431A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244645 | |||||||
chr3:57244753 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0059 |
3 | HG00099.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.475-1323A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244753 | |||||||
chr3:57244967 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.475-1109A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57244967 | |||||||
chr3:57245093 | A | G | 30 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(27): Show |
37 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.475-983A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245093 | |||||||
chr3:57245522 | G | A | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.475-554G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245522 | |||||||
chr3:57245547 | A | AT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0076 a0002c0002t0003g0057 |
3 | HG03669.hp2 HG03927.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.475-529_475-528ins others(1): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245547 | |||||||
chr3:57245547 | AG | A | 29 | a0001c0001t0001g0059 a0001c0001t0004g0011 a0001c0001t0004g0012 others(26): Show |
36 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.475-528delG | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245547 | |||||||
chr3:57245548 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(70): Show |
99 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.475-528G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245548 | |||||||
chr3:57245652 | C | G | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.475-424C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245652 | |||||||
chr3:57245659 | C | T | 1 | a0001c0001t0019g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.475-417C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245659 | |||||||
chr3:57245668 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0137 |
3 | HG00099.hp1 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.475-408C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245668 | |||||||
chr3:57245718 | T | C | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-358T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245718 | |||||||
chr3:57245733 | G | A | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.475-343G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245733 | |||||||
chr3:57245735 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475-341C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245735 | |||||||
chr3:57245911 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.475-165G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 7/21 | chr3 | 57245911 | |||||||
chr3:57246227 | A | G | 20 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(17): Show |
28 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.621+5A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246227 | |||||||
chr3:57246518 | C | T | 1 | a0001c0001t0004g0011 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.621+296C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246518 | |||||||
chr3:57246707 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.621+485T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246707 | |||||||
chr3:57246818 | C | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-577C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246818 | |||||||
chr3:57246935 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.622-460T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246935 | |||||||
chr3:57246950 | G | T | 1 | a0001c0001t0004g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.622-445G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246950 | |||||||
chr3:57246989 | TC | T | 6 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0150 others(3): Show |
6 | HG00642.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.622-405delC | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57246989 | |||||||
chr3:57246990 | C | CA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(34): Show |
53 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.622-388dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 57246990 | ||||||
chr3:57247092 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.622-303T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 8/21 | chr3 | 57247092 | |||||||
chr3:57247555 | T | C | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.704+78T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57247555 | |||||||
chr3:57247569 | C | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+92C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57247569 | |||||||
chr3:57247777 | T | C | 3 | a0001c0001t0003g0024 a0001c0001t0003g0100 a0001c0001t0003g0124 |
4 | HG01099.hp2 HG01884.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+300T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57247777 | |||||||
chr3:57247982 | T | C | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.705-211T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57247982 | |||||||
chr3:57248067 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.705-126T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57248067 | |||||||
chr3:57248120 | A | G | 1 | a0001c0001t0004g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.705-73A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 9/21 | chr3 | 57248120 | |||||||
chr3:57248644 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.863+293C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 10/21 | chr3 | 57248644 | |||||||
chr3:57248701 | C | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.863+350C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 10/21 | chr3 | 57248701 | |||||||
chr3:57248770 | T | A | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.863+419T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 10/21 | chr3 | 57248770 | |||||||
chr3:57249134 | T | C | 5 | a0003c0003t0004g0181 a0003c0003t0004g0183 a0003c0003t0004g0187 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-226T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 10/21 | chr3 | 57249134 | |||||||
chr3:57249579 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1052+31T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57249579 | |||||||
chr3:57249736 | T | C | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1052+188T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57249736 | |||||||
chr3:57249764 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1052+216A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57249764 | |||||||
chr3:57249766 | T | TA | 5 | a0001c0001t0004g0011 a0001c0001t0004g0031 a0001c0001t0004g0197 others(2): Show |
8 | HG01891.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1052+221dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57249766 | ||||||
chr3:57249970 | TGG | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
141 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1052+430_1052+431d others(4): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57249970 | ||||||
chr3:57250101 | G | C | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052+553G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250101 | |||||||
chr3:57250299 | C | T | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1052+751C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250299 | |||||||
chr3:57250316 | A | T | 1 | a0001c0001t0004g0031 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1052+768A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250316 | |||||||
chr3:57250317 | T | A | 1 | a0001c0001t0004g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1052+769T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250317 | |||||||
chr3:57250402 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0002g0160 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1052+854A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250402 | |||||||
chr3:57250796 | C | T | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1052+1248C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250796 | |||||||
chr3:57250804 | C | CT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
87 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1052+1277dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57250804 | ||||||
chr3:57250804 | C | CTT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(3): Show |
6 | HG00639.hp2 HG01346.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052+1276_1052+127 others(6): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57250804 | ||||||
chr3:57250804 | CT | C | 8 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0136 others(5): Show |
8 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052+1277delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57250804 | ||||||
chr3:57250822 | T | G | 2 | a0001c0001t0002g0111 a0001c0001t0002g0160 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1052+1274T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250822 | |||||||
chr3:57250846 | C | T | 1 | a0001c0001t0003g0024 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1052+1298C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250846 | |||||||
chr3:57250848 | C | T | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1052+1300C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250848 | |||||||
chr3:57250868 | C | A | 4 | a0001c0001t0003g0026 a0001c0001t0003g0123 a0001c0001t0003g0166 others(1): Show |
4 | HG01243.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+1320C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250868 | |||||||
chr3:57250901 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1052+1353G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250901 | |||||||
chr3:57250953 | G | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1053-1316G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250953 | |||||||
chr3:57250964 | C | T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0178 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1053-1305C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250964 | |||||||
chr3:57250997 | C | T | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1053-1272C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57250997 | |||||||
chr3:57251155 | A | G | 2 | a0001c0001t0007g0022 a0001c0001t0007g0091 |
3 | HG01884.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1053-1114A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251155 | |||||||
chr3:57251180 | C | T | 1 | a0001c0001t0023g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1053-1089C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251180 | |||||||
chr3:57251261 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1053-1008C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251261 | |||||||
chr3:57251404 | A | T | 3 | a0001c0001t0003g0024 a0001c0001t0003g0100 a0001c0001t0003g0124 |
4 | HG01099.hp2 HG01884.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-865A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251404 | |||||||
chr3:57251434 | A | G | 5 | a0001c0001t0004g0011 a0001c0001t0004g0031 a0001c0001t0004g0197 others(2): Show |
8 | HG01891.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1053-835A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251434 | |||||||
chr3:57251461 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0019g0088 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1053-808G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251461 | |||||||
chr3:57251479 | C | T | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1053-790C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251479 | |||||||
chr3:57251493 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
141 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1053-776T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251493 | |||||||
chr3:57251524 | C | CA | 13 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0066 others(10): Show |
14 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1053-726dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 57251524 | ||||||
chr3:57251754 | A | G | 1 | a0002c0002t0003g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1053-515A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251754 | |||||||
chr3:57251788 | T | A | 1 | a0001c0001t0008g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053-481T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251788 | |||||||
chr3:57251809 | C | T | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1053-460C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251809 | |||||||
chr3:57251869 | T | G | 1 | a0001c0001t0008g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053-400T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57251869 | |||||||
chr3:57252210 | G | A | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053-59G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 11/21 | chr3 | 57252210 | |||||||
chr3:57252504 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1095+193A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57252504 | |||||||
chr3:57252546 | T | G | 1 | a0001c0001t0002g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1095+235T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57252546 | |||||||
chr3:57252810 | T | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1095+499T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57252810 | |||||||
chr3:57253048 | C | A | 9 | a0001c0001t0023g0184 a0001c0001t0024g0189 a0003c0003t0004g0156 others(6): Show |
9 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-634C>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57253048 | |||||||
chr3:57253264 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1096-418C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57253264 | |||||||
chr3:57253267 | G | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1096-415G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57253267 | |||||||
chr3:57253484 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1096-198C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 12/21 | chr3 | 57253484 | |||||||
chr3:57253878 | T | G | 1 | a0002c0002t0003g0103 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1152+140T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57253878 | |||||||
chr3:57253922 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
35 | HG00639.hp2 HG01071.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.1152+184G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57253922 | |||||||
chr3:57253945 | C | T | 5 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0014g0182 others(2): Show |
6 | HG01934.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1152+207C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57253945 | |||||||
chr3:57254339 | C | T | 2 | a0001c0001t0024g0189 a0005c0010t0004g0186 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1152+601C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57254339 | |||||||
chr3:57254508 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1152+770G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57254508 | |||||||
chr3:57254774 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0048 |
2 | NA18940.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1152+1036G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57254774 | |||||||
chr3:57254844 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1152+1106T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57254844 | |||||||
chr3:57255256 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1152+1518T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255256 | |||||||
chr3:57255360 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1153-1597T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255360 | |||||||
chr3:57255494 | G | A | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1463G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255494 | |||||||
chr3:57255690 | G | A | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1153-1267G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255690 | |||||||
chr3:57255788 | A | G | 3 | a0001c0001t0006g0200 a0001c0001t0006g0205 a0001c0001t0006g0206 |
3 | HG02818.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1153-1169A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255788 | |||||||
chr3:57255982 | T | G | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1153-975T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57255982 | |||||||
chr3:57256328 | AT | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
138 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.1153-623delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr3 | 57256328 | ||||||
chr3:57256472 | T | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0160 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1153-485T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57256472 | |||||||
chr3:57256836 | A | C | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-121A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57256836 | |||||||
chr3:57256837 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1153-120G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57256837 | |||||||
chr3:57256840 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1153-117G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 13/21 | chr3 | 57256840 | |||||||
chr3:57257080 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0063 others(1): Show |
4 | HG02080.hp2 HG02135.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247+29A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 14/21 | chr3 | 57257080 | |||||||
chr3:57257091 | C | G | 3 | a0001c0001t0003g0024 a0001c0001t0003g0100 a0001c0001t0003g0124 |
4 | HG01099.hp2 HG01884.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247+40C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 14/21 | chr3 | 57257091 | |||||||
chr3:57257190 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1248-56A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 14/21 | chr3 | 57257190 | |||||||
chr3:57257463 | G | C | 3 | a0001c0001t0002g0130 a0001c0001t0002g0168 a0001c0009t0002g0098 |
3 | HG01358.hp1 HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1430+35G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57257463 | |||||||
chr3:57257598 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1430+170A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57257598 | |||||||
chr3:57257802 | C | T | 2 | a0001c0001t0014g0182 a0001c0001t0014g0185 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1430+374C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57257802 | |||||||
chr3:57257887 | A | G | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1430+459A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57257887 | |||||||
chr3:57258391 | G | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
95 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1431-637G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57258391 | |||||||
chr3:57258984 | A | T | 2 | a0001c0001t0002g0087 a0001c0001t0019g0088 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1431-44A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 15/21 | chr3 | 57258984 | |||||||
chr3:57259269 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
95 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1483+189T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 16/21 | chr3 | 57259269 | |||||||
chr3:57259460 | T | TTG | 6 | a0001c0001t0001g0047 a0001c0004t0009g0153 a0001c0004t0009g0154 others(3): Show |
6 | HG01109.hp1 HG02040.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-367_1484-366d others(4): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 57259460 | ||||||
chr3:57259551 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1484-294C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 16/21 | chr3 | 57259551 | |||||||
chr3:57259774 | A | G | 12 | a0002c0002t0003g0004 a0002c0002t0003g0005 a0002c0002t0003g0023 others(9): Show |
19 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1484-71A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 16/21 | chr3 | 57259774 | |||||||
chr3:57260057 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
95 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1658+38C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 17/21 | chr3 | 57260057 | |||||||
chr3:57260201 | T | C | 20 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(17): Show |
28 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1695+48T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 18/21 | chr3 | 57260201 | |||||||
chr3:57260236 | G | A | 1 | a0001c0001t0020g0037 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1695+83G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 18/21 | chr3 | 57260236 | |||||||
chr3:57260267 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1695+114T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 18/21 | chr3 | 57260267 | |||||||
chr3:57260856 | CAAATT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1842+89_1842+93del others(5): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57260856 | ||||||
chr3:57260864 | ATTAG | A | 3 | a0001c0001t0002g0087 a0001c0001t0019g0088 a0001c0001t0024g0189 |
3 | HG02486.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1842+96_1842+99del others(4): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57260864 | ||||||
chr3:57261086 | G | A | 27 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(24): Show |
39 | HG00280.hp2 HG00738.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1842+312G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261086 | |||||||
chr3:57261094 | TC | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+321delC | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261094 | |||||||
chr3:57261101 | C | T | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1842+327C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261101 | |||||||
chr3:57261165 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1842+391C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261165 | |||||||
chr3:57261240 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1842+466G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261240 | |||||||
chr3:57261500 | A | G | 2 | a0001c0001t0002g0112 a0001c0001t0002g0146 |
2 | HG02132.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1842+726A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261500 | |||||||
chr3:57261601 | C | G | 25 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(22): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1842+827C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261601 | |||||||
chr3:57261620 | G | A | 32 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(29): Show |
41 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1842+846G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261620 | |||||||
chr3:57261647 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1842+873T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261647 | |||||||
chr3:57261813 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1842+1039C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261813 | |||||||
chr3:57261924 | A | G | 25 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(22): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1842+1150A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261924 | |||||||
chr3:57261930 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1842+1156G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57261930 | |||||||
chr3:57262050 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1842+1276C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262050 | |||||||
chr3:57262092 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1842+1318C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262092 | |||||||
chr3:57262229 | T | C | 7 | a0001c0001t0005g0010 a0001c0001t0005g0119 a0001c0001t0005g0164 others(4): Show |
9 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1842+1455T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262229 | |||||||
chr3:57262235 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1842+1461A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262235 | |||||||
chr3:57262385 | C | CTTT | 5 | a0001c0001t0001g0050 a0001c0001t0004g0203 a0001c0001t0006g0206 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1842+1634_1842+163 others(7): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(70): Show |
109 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1842+1633_1842+163 others(8): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTT | 48 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0034 others(45): Show |
61 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.1842+1632_1842+163 others(9): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTT | 5 | a0001c0001t0001g0075 a0001c0001t0003g0105 a0001c0001t0003g0159 others(2): Show |
5 | HG01358.hp2 HG01433.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+1631_1842+163 others(10): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0015g0116 a0001c0001t0018g0102 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1842+1626_1842+163 others(15): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1842+1624_1842+163 others(17): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0087 a0001c0001t0002g0125 a0001c0001t0002g0160 |
3 | HG01109.hp2 HG02683.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1842+1623_1842+163 others(18): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0019g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1842+1622_1842+163 others(19): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0008g0113 a0001c0001t0016g0120 a0001c0001t0017g0161 others(1): Show |
4 | HG02280.hp1 HG03927.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+1620_1842+163 others(21): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0002g0115 a0001c0001t0002g0118 a0001c0001t0002g0163 others(1): Show |
4 | HG00735.hp2 HG02647.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+1619_1842+163 others(22): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(12): Show |
10 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0002g0006 others(7): Show |
12 | HG01081.hp2 HG02132.hp2 HG03195.hp2 others(9): Show |
intron_variant | MODIFIER | c.1842+1618_1842+163 others(23): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(13): Show |
11 | a0001c0001t0001g0016 a0001c0001t0002g0027 a0001c0001t0002g0028 others(8): Show |
14 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.1842+1617_1842+163 others(24): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(14): Show |
6 | a0001c0001t0001g0041 a0001c0001t0002g0137 a0001c0001t0002g0138 others(3): Show |
6 | HG01516.hp2 HG04115.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842+1616_1842+163 others(25): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0002g0110 a0001c0001t0002g0149 a0001c0001t0002g0173 others(1): Show |
4 | HG02055.hp2 HG03942.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1615_1842+163 others(26): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0002g0029 a0001c0001t0002g0167 a0001c0001t0008g0114 |
4 | HG02258.hp2 HG02970.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1614_1842+163 others(27): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1842+1613_1842+163 others(28): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0002g0134 a0001c0009t0002g0098 a0006c0007t0002g0194 |
3 | HG01071.hp2 HG01358.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1842+1612_1842+163 others(29): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0002g0127 a0001c0001t0002g0169 |
2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1842+1636_1842+163 others(30): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(20): Show |
3 | a0001c0001t0001g0040 a0001c0001t0002g0130 a0001c0001t0002g0145 |
3 | HG00609.hp2 HG01928.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1842+1636_1842+163 others(31): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1842+1636_1842+163 others(32): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1842+1636_1842+163 others(33): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0002g0179 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1842+1636_1842+163 others(34): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(24): Show |
2 | a0001c0001t0002g0131 a0001c0001t0002g0135 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1842+1636_1842+163 others(35): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1842+1636_1842+163 others(36): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0002g0170 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1842+1636_1842+163 others(37): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262385 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0002g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1842+1636_1842+163 others(40): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262385 | ||||||
chr3:57262421 | C | T | 25 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(22): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1842+1647C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262421 | |||||||
chr3:57262511 | G | GC | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1842+1738dupC | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262511 | ||||||
chr3:57262572 | G | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1842+1798G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262572 | |||||||
chr3:57262590 | T | A | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1842+1816T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262590 | |||||||
chr3:57262724 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
96 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1842+1950C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262724 | |||||||
chr3:57262794 | G | T | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1842+2020G>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262794 | |||||||
chr3:57262809 | A | C | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1842+2035A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262809 | |||||||
chr3:57262810 | AGGGGTGT others(3): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1842+2037_1842+204 others(14): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262810 | |||||||
chr3:57262813 | G | GGT | 3 | a0001c0001t0002g0087 a0001c0001t0002g0111 a0001c0001t0002g0141 |
3 | HG02809.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1842+2072_1842+207 others(6): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262813 | ||||||
chr3:57262813 | GGTGT | G | 12 | a0001c0001t0002g0109 a0001c0001t0002g0157 a0001c0001t0002g0163 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1842+2070_1842+207 others(8): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262813 | ||||||
chr3:57262813 | GGTGTGT | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
119 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.1842+2068_1842+207 others(10): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262813 | ||||||
chr3:57262813 | GGTGTGTG others(1): Show |
G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(34): Show |
50 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.1842+2066_1842+207 others(12): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262813 | ||||||
chr3:57262813 | GGTGTGTG others(11): Show |
G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
6 | HG01934.hp2 HG02040.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842+2056_1842+207 others(22): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262813 | ||||||
chr3:57262846 | G | A | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+2072G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262846 | |||||||
chr3:57262848 | A | G | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1842+2074A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262848 | |||||||
chr3:57262851 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1842+2077C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262851 | |||||||
chr3:57262852 | AT | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1842+2093delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57262852 | ||||||
chr3:57262867 | T | C | 5 | a0001c0004t0009g0153 a0001c0004t0009g0154 a0001c0004t0009g0180 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+2093T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262867 | |||||||
chr3:57262955 | G | A | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1842+2181G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57262955 | |||||||
chr3:57263034 | A | G | 1 | a0001c0001t0014g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1842+2260A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263034 | |||||||
chr3:57263142 | C | T | 1 | a0001c0001t0024g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1842+2368C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263142 | |||||||
chr3:57263157 | A | G | 1 | a0001c0001t0008g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1842+2383A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263157 | |||||||
chr3:57263203 | C | T | 2 | a0001c0004t0013g0152 a0001c0004t0013g0155 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1842+2429C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263203 | |||||||
chr3:57263362 | A | AT | 7 | a0001c0001t0014g0182 a0001c0001t0014g0185 a0001c0004t0009g0153 others(4): Show |
7 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1842+2600dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57263362 | ||||||
chr3:57263559 | G | A | 25 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(22): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1842+2785G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263559 | |||||||
chr3:57263590 | C | G | 1 | a0001c0001t0004g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1842+2816C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263590 | |||||||
chr3:57263637 | ACATTTTC others(6): Show |
A | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1842+2880_1842+289 others(17): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57263637 | ||||||
chr3:57263709 | G | A | 1 | a0001c0001t0012g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1842+2935G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263709 | |||||||
chr3:57263712 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1842+2938G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263712 | |||||||
chr3:57263725 | TTG | T | 2 | a0001c0001t0014g0182 a0001c0001t0014g0185 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1842+2963_1842+296 others(6): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57263725 | ||||||
chr3:57263765 | GT | G | 35 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(32): Show |
44 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.1842+3005delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57263765 | ||||||
chr3:57263768 | T | G | 25 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(22): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1842+2994T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263768 | |||||||
chr3:57263769 | T | G | 2 | a0001c0001t0014g0182 a0001c0001t0014g0185 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1842+2995T>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57263769 | |||||||
chr3:57264157 | T | TATA | 1 | a0001c0001t0001g0008 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1842+3383_1842+338 others(7): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264157 | |||||||
chr3:57264376 | T | C | 1 | a0002c0002t0003g0023 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1843-3366T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264376 | |||||||
chr3:57264560 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1843-3182A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264560 | |||||||
chr3:57264563 | T | A | 5 | a0002c0002t0003g0004 a0002c0002t0003g0096 a0002c0002t0003g0103 others(2): Show |
8 | HG00280.hp2 HG01192.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843-3179T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264563 | |||||||
chr3:57264564 | A | T | 2 | a0001c0001t0002g0101 a0001c0006t0002g0117 |
2 | HG03209.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1843-3178A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264564 | |||||||
chr3:57264582 | TA | T | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1843-3151delA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57264582 | ||||||
chr3:57264591 | AT | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0160 a0001c0001t0003g0097 |
3 | HG01109.hp2 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1843-3144delT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57264591 | ||||||
chr3:57264592 | T | A | 24 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0093 others(21): Show |
36 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1843-3150T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264592 | |||||||
chr3:57264598 | T | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0040 others(106): Show |
132 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1843-3144T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264598 | |||||||
chr3:57264599 | A | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0001g0077 others(2): Show |
5 | HG02486.hp1 HG03516.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-3143A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264599 | |||||||
chr3:57264638 | T | A | 7 | a0001c0001t0005g0010 a0001c0001t0005g0119 a0001c0001t0005g0164 others(4): Show |
9 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1843-3104T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264638 | |||||||
chr3:57264742 | C | T | 1 | a0001c0001t0004g0204 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1843-3000C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264742 | |||||||
chr3:57264743 | G | A | 3 | a0001c0001t0010g0030 a0001c0001t0010g0191 a0001c0001t0022g0192 |
4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843-2999G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57264743 | |||||||
chr3:57264801 | C | CT | 6 | a0001c0001t0001g0053 a0001c0001t0003g0123 a0001c0001t0005g0010 others(3): Show |
8 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843-2925dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57264801 | ||||||
chr3:57265127 | C | T | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1843-2615C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265127 | |||||||
chr3:57265190 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0074 |
2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1843-2552C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265190 | |||||||
chr3:57265218 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1843-2524G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265218 | |||||||
chr3:57265436 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1843-2306C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265436 | |||||||
chr3:57265488 | T | C | 2 | a0001c0001t0012g0033 a0001c0001t0012g0089 |
2 | HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1843-2254T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265488 | |||||||
chr3:57265528 | ATTACT | A | 2 | a0001c0001t0014g0182 a0001c0001t0014g0185 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1843-2210_1843-220 others(9): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57265528 | ||||||
chr3:57265540 | A | C | 2 | a0001c0004t0013g0152 a0001c0004t0013g0155 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1843-2202A>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265540 | |||||||
chr3:57265655 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1843-2087G>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265655 | |||||||
chr3:57265919 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02698.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1843-1823T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57265919 | |||||||
chr3:57266635 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1843-1107T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57266635 | |||||||
chr3:57266804 | A | G | 5 | a0003c0003t0004g0181 a0003c0003t0004g0183 a0003c0003t0004g0187 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-938A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57266804 | |||||||
chr3:57267028 | A | AT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1843-713dupT | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 57267028 | ||||||
chr3:57267119 | A | T | 1 | a0005c0010t0004g0186 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1843-623A>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 19/21 | chr3 | 57267119 | |||||||
chr3:57267857 | C | T | 1 | a0001c0001t0004g0031 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1893+65C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 20/21 | chr3 | 57267857 | |||||||
chr3:57267927 | A | G | 4 | a0001c0001t0004g0032 a0001c0001t0004g0201 a0001c0001t0004g0204 others(1): Show |
5 | HG02647.hp2 HG03486.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+135A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 20/21 | chr3 | 57267927 | |||||||
chr3:57267966 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1893+174C>T | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 20/21 | chr3 | 57267966 | |||||||
chr3:57268092 | C | CA | 27 | a0001c0001t0002g0101 a0001c0001t0002g0157 a0001c0001t0004g0011 others(24): Show |
36 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1894-294dupA | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 57268092 | ||||||
chr3:57268851 | A | G | 2 | a0001c0001t0004g0012 a0001c0001t0004g0203 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1983+364A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57268851 | |||||||
chr3:57268916 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1983+429T>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57268916 | |||||||
chr3:57268926 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1983+439A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57268926 | |||||||
chr3:57268940 | C | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0026 others(25): Show |
41 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1983+453C>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57268940 | |||||||
chr3:57268965 | T | A | 34 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0031 others(31): Show |
43 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1983+478T>A | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57268965 | |||||||
chr3:57269066 | G | C | 1 | a0001c0001t0001g0042 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1984-475G>C | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57269066 | |||||||
chr3:57269178 | A | G | 1 | a0002c0002t0003g0023 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1984-363A>G | APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | chr3 | 57269178 | |||||||
chr3:57269450 | A | AGAATT | 68 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0026 others(65): Show |
90 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(87): Show |
intron_variant | MODIFIER | c.1984-88_1984-87ins others(5): Show |
APPL1 | ENSG00000157500.12 | transcript | ENST00000288266.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr3 | 57269450 |