Item | Value |
---|---|
geneid | 23192 |
ensemblid | ENSG00000168397.17 |
hgncid | 20790 |
symbol | ATG4B |
name | autophagy related 4B cysteine peptidase |
refseq_nuc | NM_013325.5 |
refseq_prot | NP_037457.3 |
ensembl_nuc | ENST00000404914.8 |
ensembl_prot | ENSP00000384259.3 |
mane_status | MANE Select |
chr | chr2 |
start | 241637693 |
end | 241673857 |
strand | + |
ver | v1.2 |
region | chr2:241637693-241673857 |
region5000 | chr2:241632693-241678857 |
regionname0 | ATG4B_chr2_241637693_241673857 |
regionname5000 | ATG4B_chr2_241632693_241678857 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 393 | 324 | 70 | 57 | 151 | 11 | 34 | 112 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
a0002 | 1/0 | 393 | 58 | 4 | 7 | 37 | 3 | 6 | 35 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
a0003 | 0/0 | 393 | 25 | 13 | 1 | 7 | 2 | 2 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
a0004 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
a0005 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
a0006 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | MDAAT others(388): Show |
chr2 | 241632693 | 241678857 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1179 | 223 | 58 | 45 | 86 | 6 | 27 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0001c0002 | 0/0 | 1179 | 87 | 10 | 10 | 56 | 5 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0001c0005 | 0/0 | 1179 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0001c0006 | 0/0 | 1179 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0001c0007 | 0/0 | 1179 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0001c0010 | 0/0 | 1179 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0002c0003 | 1/0 | 1179 | 58 | 4 | 7 | 37 | 3 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0003c0004 | 0/0 | 1179 | 23 | 11 | 1 | 7 | 2 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0003c0008 | 0/0 | 1179 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0004c0009 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0005c0012 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 | ||
a0006c0011 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | ATGGA others(1174): Show |
chr2 | 241632693 | 241678857 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2796 | 88 | 11 | 36 | 28 | 4 | 9 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0003 | 0/0 | 2793 | 73 | 9 | 4 | 45 | 2 | 13 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0004 | 0/0 | 2796 | 11 | 9 | 1 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0005 | 0/0 | 2792 | 17 | 16 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2787): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0008 | 0/0 | 2792 | 8 | 0 | 0 | 8 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2787): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0010 | 0/1 | 2796 | 5 | 3 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0011 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2792): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0015 | 0/0 | 2795 | 3 | 1 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2790): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0016 | 0/0 | 2795 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2790): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0017 | 0/0 | 2792 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2787): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0019 | 0/0 | 2794 | 2 | 0 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2789): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0020 | 0/0 | 2793 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0027 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0031 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0032 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2792): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0033 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2792): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0035 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0036 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0037 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2790): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0038 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0001t0039 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0002 | 0/0 | 2799 | 73 | 7 | 8 | 48 | 4 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0012 | 0/0 | 2799 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0014 | 0/0 | 2799 | 3 | 1 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0021 | 0/0 | 2799 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0022 | 0/0 | 2799 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0024 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0028 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0029 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0030 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0002t0043 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0005t0002 | 0/0 | 2799 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0006t0002 | 0/0 | 2799 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0007t0002 | 0/0 | 2799 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0001c0010t0003 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2788): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0004 | 0/0 | 2796 | 35 | 2 | 5 | 24 | 3 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0007 | 0/0 | 2796 | 12 | 0 | 0 | 12 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0011 | 1/0 | 2797 | 4 | 0 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2792): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0013 | 0/0 | 2796 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0040 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0041 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0002c0003t0042 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2792): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0006 | 0/0 | 2796 | 11 | 0 | 1 | 7 | 2 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0009 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0023 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0025 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0026 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0004t0034 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0003c0008t0018 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0004c0009t0001 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
a0005c0012t0012 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2794): Show |
chr2 | 241632693 | 241678857 |
a0006c0011t0006 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | AGTCG others(2791): Show |
chr2 | 241632693 | 241678857 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0039 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0010g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0010g0324 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0015g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0015g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0016g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0017g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0019g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0020g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0027g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0031g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0032g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0033g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0035g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0036g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0037g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0038g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0039g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0012g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0014g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0021g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0022g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0024g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0028g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0029g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0030g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0043g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0010t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0011g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0011g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0013g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0013g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0040g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0041g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0042g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0023g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0025g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0026g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0034g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0008t0018g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0008t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0004c0009t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0005c0012t0012g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0006c0011t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0039 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0159 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00140 | hp1 | a0002 | c0003 | t0004 | g0191 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00140 | hp2 | a0002 | c0003 | t0004 | g0028 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0152 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0138 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00438 | hp1 | a0001 | c0002 | t0021 | g0151 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00438 | hp2 | a0001 | c0001 | t0036 | g0249 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00544 | hp1 | a0001 | c0001 | t0032 | g0309 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00597 | hp1 | a0001 | c0002 | t0012 | g0147 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00621 | hp1 | a0001 | c0002 | t0024 | g0079 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00621 | hp2 | a0001 | c0002 | t0012 | g0155 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0041 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00735 | hp1 | a0002 | c0003 | t0004 | g0013 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00741 | hp1 | a0002 | c0003 | t0013 | g0333 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01071 | hp1 | a0002 | c0003 | t0013 | g0045 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01099 | hp1 | a0003 | c0004 | t0006 | g0102 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01106 | hp1 | a0001 | c0002 | t0022 | g0004 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01109 | hp1 | a0001 | c0006 | t0002 | g0210 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01167 | hp1 | a0002 | c0003 | t0004 | g0013 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0212 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0215 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01255 | hp2 | a0004 | c0009 | t0001 | g0177 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0206 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01496 | hp1 | a0001 | c0002 | t0014 | g0030 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01496 | hp2 | a0001 | c0006 | t0002 | g0098 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01515 | hp1 | a0003 | c0004 | t0006 | g0087 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0194 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01884 | hp2 | a0002 | c0003 | t0013 | g0095 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0326 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01928 | hp2 | a0002 | c0003 | t0004 | g0023 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01952 | hp1 | a0002 | c0003 | t0004 | g0023 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02027 | hp2 | a0002 | c0003 | t0004 | g0015 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0327 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02056 | hp2 | a0003 | c0004 | t0006 | g0019 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02074 | hp2 | a0001 | c0007 | t0002 | g0066 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02080 | hp1 | a0001 | c0005 | t0002 | g0227 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02135 | hp1 | a0001 | c0002 | t0012 | g0135 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02155 | hp2 | a0002 | c0003 | t0004 | g0148 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02572 | hp1 | a0002 | c0003 | t0013 | g0045 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0308 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02615 | hp1 | a0001 | c0006 | t0002 | g0190 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02622 | hp1 | a0003 | c0004 | t0009 | g0020 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02647 | hp1 | a0003 | c0004 | t0009 | g0099 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02683 | hp2 | a0001 | c0001 | t0035 | g0006 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02738 | hp2 | a0002 | c0003 | t0004 | g0028 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02809 | hp2 | a0002 | c0003 | t0004 | g0166 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02886 | hp1 | a0003 | c0004 | t0009 | g0100 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02965 | hp1 | a0001 | c0002 | t0043 | g0106 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02970 | hp1 | a0003 | c0004 | t0025 | g0021 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03017 | hp1 | a0001 | c0010 | t0003 | g0290 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03017 | hp2 | a0002 | c0003 | t0011 | g0010 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03041 | hp1 | a0003 | c0004 | t0023 | g0091 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03041 | hp2 | a0001 | c0006 | t0002 | g0209 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03098 | hp1 | a0003 | c0004 | t0009 | g0021 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03209 | hp1 | a0003 | c0008 | t0018 | g0049 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03453 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03453 | hp2 | a0001 | c0001 | t0016 | g0044 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03490 | hp2 | a0001 | c0001 | t0020 | g0001 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03491 | hp1 | a0003 | c0004 | t0026 | g0236 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0281 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03492 | hp1 | a0001 | c0001 | t0020 | g0001 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0319 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03540 | hp2 | a0001 | c0001 | t0039 | g0262 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03579 | hp1 | a0003 | c0004 | t0009 | g0020 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03654 | hp2 | a0002 | c0003 | t0011 | g0010 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03710 | hp2 | a0002 | c0003 | t0040 | g0014 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03831 | hp2 | a0002 | c0003 | t0041 | g0187 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0193 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03927 | hp1 | a0001 | c0001 | t0019 | g0001 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03942 | hp2 | a0003 | c0004 | t0006 | g0083 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04204 | hp1 | a0002 | c0003 | t0011 | g0010 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0040 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18906 | hp1 | a0003 | c0008 | t0018 | g0048 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18906 | hp2 | a0001 | c0001 | t0037 | g0214 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18939 | hp1 | a0001 | c0005 | t0002 | g0092 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18941 | hp1 | a0003 | c0004 | t0006 | g0096 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18943 | hp1 | a0002 | c0003 | t0004 | g0202 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18946 | hp1 | a0001 | c0007 | t0002 | g0073 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18946 | hp2 | a0002 | c0003 | t0007 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18947 | hp1 | a0002 | c0003 | t0004 | g0204 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18949 | hp2 | a0002 | c0003 | t0007 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18951 | hp1 | a0001 | c0002 | t0029 | g0026 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18954 | hp1 | a0001 | c0005 | t0002 | g0097 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18954 | hp2 | a0002 | c0003 | t0004 | g0171 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18957 | hp1 | a0002 | c0003 | t0007 | g0056 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18959 | hp1 | a0003 | c0004 | t0006 | g0086 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0232 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18961 | hp1 | a0002 | c0003 | t0007 | g0055 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18963 | hp2 | a0002 | c0003 | t0004 | g0170 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18964 | hp1 | a0002 | c0003 | t0007 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18965 | hp2 | a0002 | c0003 | t0007 | g0052 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18966 | hp1 | a0003 | c0004 | t0006 | g0088 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18969 | hp1 | a0002 | c0003 | t0004 | g0150 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18971 | hp1 | a0001 | c0007 | t0002 | g0067 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18977 | hp1 | a0003 | c0004 | t0006 | g0101 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18978 | hp1 | a0002 | c0003 | t0007 | g0053 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18979 | hp1 | a0002 | c0003 | t0004 | g0229 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18981 | hp2 | a0002 | c0003 | t0004 | g0015 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18984 | hp1 | a0002 | c0003 | t0004 | g0165 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18985 | hp2 | a0002 | c0003 | t0004 | g0200 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18987 | hp1 | a0002 | c0003 | t0004 | g0134 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18987 | hp2 | a0002 | c0003 | t0004 | g0163 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18989 | hp1 | a0003 | c0004 | t0006 | g0094 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18990 | hp1 | a0002 | c0003 | t0007 | g0054 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18990 | hp2 | a0001 | c0001 | t0027 | g0003 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18992 | hp1 | a0002 | c0003 | t0004 | g0172 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18994 | hp2 | a0001 | c0001 | t0019 | g0295 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18999 | hp1 | a0002 | c0003 | t0007 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19005 | hp1 | a0002 | c0003 | t0004 | g0015 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19006 | hp2 | a0005 | c0012 | t0012 | g0137 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19007 | hp2 | a0001 | c0005 | t0002 | g0090 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19009 | hp1 | a0003 | c0004 | t0006 | g0019 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19011 | hp2 | a0002 | c0003 | t0004 | g0201 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19012 | hp1 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19030 | hp1 | a0003 | c0004 | t0009 | g0084 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0211 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19043 | hp1 | a0001 | c0001 | t0038 | g0276 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19043 | hp2 | a0001 | c0002 | t0030 | g0311 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19055 | hp1 | a0002 | c0003 | t0004 | g0203 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19056 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19064 | hp1 | a0001 | c0002 | t0021 | g0141 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19066 | hp2 | a0002 | c0003 | t0004 | g0168 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19067 | hp1 | a0001 | c0001 | t0008 | g0230 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19068 | hp1 | a0002 | c0003 | t0004 | g0140 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19068 | hp2 | a0001 | c0007 | t0002 | g0074 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19075 | hp1 | a0002 | c0003 | t0042 | g0208 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19076 | hp2 | a0002 | c0003 | t0007 | g0057 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19077 | hp1 | a0002 | c0003 | t0007 | g0058 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19080 | hp1 | a0001 | c0001 | t0008 | g0231 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19080 | hp2 | a0002 | c0003 | t0004 | g0275 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19081 | hp1 | a0002 | c0003 | t0007 | g0051 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19081 | hp2 | a0002 | c0003 | t0004 | g0266 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19083 | hp1 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19090 | hp1 | a0001 | c0002 | t0028 | g0075 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19091 | hp1 | a0002 | c0003 | t0004 | g0167 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ASW | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20129 | hp2 | a0002 | c0003 | t0004 | g0219 | AFR | ASW | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0117 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20752 | hp2 | a0003 | c0004 | t0006 | g0085 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20805 | hp2 | a0001 | c0002 | t0014 | g0030 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | GIH | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01123 | hp1 | a0002 | c0003 | t0004 | g0013 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02486 | hp2 | a0001 | c0001 | t0015 | g0213 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02559 | hp2 | a0003 | c0004 | t0009 | g0093 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03471 | hp1 | a0001 | c0001 | t0016 | g0044 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03471 | hp2 | a0001 | c0001 | t0017 | g0025 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG06807 | hp1 | a0003 | c0004 | t0009 | g0089 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18955 | hp1 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18955 | hp2 | a0001 | c0005 | t0002 | g0064 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20300 | hp2 | a0003 | c0004 | t0034 | g0103 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA21309 | hp1 | a0006 | c0011 | t0006 | g0303 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA21309 | hp2 | a0001 | c0002 | t0014 | g0185 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0324 | REF | REF | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
homoSapiens | grch38p0 | a0002 | c0003 | t0011 | g0108 | REF | REF | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241651022 | A | G | 1 | a0005 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.23A>G | p.Tyr8Cys | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 2/13 | 45/2797 | 23/1182 | 8/393 | chr2 | 241651022 | |||
chr2:241653596 | G | A | 1 | a0004 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.269G>A | p.Arg90Gln | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/13 | 291/2797 | 269/1182 | 90/393 | chr2 | 241653596 | |||
chr2:241670757 | A | G | 2 | a0003 a0006 |
26 | HG01099.hp1 HG01515.hp1 HG02056.hp2 others(23): Show |
missense_variant | MODERATE | c.989A>G | p.Asn330Ser | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/13 | 1011/2797 | 989/1182 | 330/393 | chr2 | 241670757 | |||
chr2:241671358 | T | A | 5 | a0001 a0003 a0004 others(2): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
missense_variant | MODERATE | c.1061T>A | p.Leu354Gln | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1083/2797 | 1061/1182 | 354/393 | chr2 | 241671358 | |||
chr2:241671379 | G | T | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1082G>T | p.Cys361Phe | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1104/2797 | 1082/1182 | 361/393 | chr2 | 241671379 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241654571 | G | A | 1 | a0001c0006 | 4 | HG01109.hp1 HG01496.hp2 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.309G>A | p.Arg103Arg | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/13 | 331/2797 | 309/1182 | 103/393 | chr2 | 241654571 | |||
chr2:241666718 | C | T | 2 | a0001c0007 a0003c0008 |
6 | HG02074.hp2 HG03209.hp1 NA18906.hp1 others(3): Show |
synonymous_variant | LOW | c.612C>T | p.Asn204Asn | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/13 | 634/2797 | 612/1182 | 204/393 | chr2 | 241666718 | |||
chr2:241666760 | A | G | 1 | a0001c0005 | 5 | HG02080.hp1 NA18939.hp1 NA18954.hp1 others(2): Show |
synonymous_variant | LOW | c.654A>G | p.Pro218Pro | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/13 | 676/2797 | 654/1182 | 218/393 | chr2 | 241666760 | |||
chr2:241671314 | G | A | 1 | a0001c0010 | 1 | HG03017.hp1 | splice_region_variant&synonymous_variant | LOW | c.1017G>A | p.Leu339Leu | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1039/2797 | 1017/1182 | 339/393 | chr2 | 241671314 | |||
chr2:241671323 | T | C | 5 | a0001c0002 a0001c0005 a0001c0006 others(2): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
synonymous_variant | LOW | c.1026T>C | p.Leu342Leu | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1048/2797 | 1026/1182 | 342/393 | chr2 | 241671323 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241637703 | C | T | 1 | a0001c0002t0021 | 2 | HG00438.hp1 NA19064.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/13 | chr2 | 241637703 | |||||||
chr2:241672491 | C | T | 1 | a0001c0002t0043 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 227 | chr2 | 241672491 | ||||||
chr2:241672519 | T | C | 33 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(30): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*255T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 255 | chr2 | 241672519 | ||||||
chr2:241672543 | G | A | 1 | a0001c0002t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 279 | chr2 | 241672543 | ||||||
chr2:241672584 | C | T | 7 | a0001c0002t0002 a0001c0002t0012 a0001c0002t0021 others(4): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*320C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 320 | chr2 | 241672584 | ||||||
chr2:241672648 | T | TG | 29 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0027 others(26): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*387dupG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 388 | INFO_REALIGN_3_PRIME | chr2 | 241672648 | |||||
chr2:241672716 | T | C | 1 | a0003c0004t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 452 | chr2 | 241672716 | ||||||
chr2:241672736 | C | T | 1 | a0001c0002t0014 | 3 | HG01496.hp1 NA20805.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 472 | chr2 | 241672736 | ||||||
chr2:241672766 | C | T | 1 | a0003c0004t0034 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 502 | chr2 | 241672766 | ||||||
chr2:241672927 | G | T | 30 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0020 others(27): Show |
226 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*663G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 663 | chr2 | 241672927 | ||||||
chr2:241673040 | CG | C | 9 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0032 others(6): Show |
68 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*786delG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 786 | INFO_REALIGN_3_PRIME | chr2 | 241673040 | |||||
chr2:241673040 | CGG | C | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(37): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786delGG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 785 | INFO_REALIGN_3_PRIME | chr2 | 241673040 | |||||
chr2:241673045 | G | C | 1 | a0001c0002t0024 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*781G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 781 | chr2 | 241673045 | ||||||
chr2:241673072 | C | T | 29 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0027 others(26): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*808C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 808 | chr2 | 241673072 | ||||||
chr2:241673140 | G | C | 1 | a0002c0003t0042 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*876G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 876 | chr2 | 241673140 | ||||||
chr2:241673152 | C | T | 4 | a0001c0001t0038 a0001c0001t0039 a0001c0002t0012 others(1): Show |
6 | HG00597.hp1 HG00621.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*888C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 888 | chr2 | 241673152 | ||||||
chr2:241673203 | TGTG | T | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 |
27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*945delGTG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 943 | INFO_REALIGN_3_PRIME | chr2 | 241673203 | |||||
chr2:241673340 | G | A | 12 | a0001c0001t0001 a0001c0001t0027 a0001c0001t0032 others(9): Show |
117 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1076G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1076 | chr2 | 241673340 | ||||||
chr2:241673342 | T | G | 1 | a0001c0001t0038 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1078 | chr2 | 241673342 | ||||||
chr2:241673369 | T | G | 29 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0016 others(26): Show |
226 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1105T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1105 | chr2 | 241673369 | ||||||
chr2:241673415 | G | A | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0015 |
28 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1151G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1151 | chr2 | 241673415 | ||||||
chr2:241673420 | T | C | 14 | a0001c0002t0002 a0001c0002t0012 a0001c0002t0014 others(11): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1156T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1156 | chr2 | 241673420 | ||||||
chr2:241673457 | C | CGCT | 14 | a0001c0002t0002 a0001c0002t0012 a0001c0002t0014 others(11): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1211dupGCT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1212 | INFO_REALIGN_3_PRIME | chr2 | 241673457 | |||||
chr2:241673485 | C | T | 1 | a0001c0001t0027 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1221C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1221 | chr2 | 241673485 | ||||||
chr2:241673493 | C | T | 1 | a0001c0001t0017 | 2 | HG03453.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1229 | chr2 | 241673493 | ||||||
chr2:241673494 | A | G | 33 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(30): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*1230A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1230 | chr2 | 241673494 | ||||||
chr2:241673504 | G | A | 1 | a0001c0002t0028 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1240 | chr2 | 241673504 | ||||||
chr2:241673583 | CAT | C | 8 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0020 others(5): Show |
82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1321_*1322delTA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1321 | INFO_REALIGN_3_PRIME | chr2 | 241673583 | |||||
chr2:241673598 | C | G | 1 | a0001c0001t0036 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1334 | chr2 | 241673598 | ||||||
chr2:241673674 | A | G | 26 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0016 others(23): Show |
205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1410A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1410 | chr2 | 241673674 | ||||||
chr2:241673718 | T | G | 29 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(26): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1454T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1454 | chr2 | 241673718 | ||||||
chr2:241673763 | T | G | 1 | a0001c0002t0029 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1499T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1499 | chr2 | 241673763 | ||||||
chr2:241673812 | G | A | 1 | a0003c0004t0025 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1548 | chr2 | 241673812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241637840 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.10+116C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241637840 | |||||||
chr2:241637872 | G | GGGGCGGT others(13): Show |
2 | a0002c0003t0013g0045 a0002c0003t0013g0333 |
3 | HG00741.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.10+157_10+176dupTT others(18): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241637872 | ||||||
chr2:241637943 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10+219C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241637943 | |||||||
chr2:241638014 | C | CCCTTGCG others(26): Show |
1 | a0001c0001t0001g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+299_10+300insTC others(31): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241638014 | ||||||
chr2:241638059 | G | C | 1 | a0001c0001t0001g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+335G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638059 | |||||||
chr2:241638146 | G | A | 1 | a0001c0001t0003g0009 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10+422G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638146 | |||||||
chr2:241638147 | C | A | 1 | a0001c0002t0002g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10+423C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638147 | |||||||
chr2:241638149 | T | C | 1 | a0001c0001t0003g0047 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.10+425T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638149 | |||||||
chr2:241638192 | G | A | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+468G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638192 | |||||||
chr2:241638250 | C | T | 41 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(38): Show |
51 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.10+526C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638250 | |||||||
chr2:241638265 | C | A | 1 | a0001c0002t0002g0050 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.10+541C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638265 | |||||||
chr2:241638370 | A | AGT | 76 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(73): Show |
88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+661_10+662dupGT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241638370 | ||||||
chr2:241638413 | C | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+689C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638413 | |||||||
chr2:241638419 | A | G | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.10+695A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638419 | |||||||
chr2:241638420 | T | C | 9 | a0002c0003t0007g0005 a0002c0003t0007g0051 a0002c0003t0007g0052 others(6): Show |
12 | NA18946.hp2 NA18949.hp2 NA18957.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+696T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638420 | |||||||
chr2:241638475 | G | T | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.10+751G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638475 | |||||||
chr2:241638482 | C | T | 1 | a0001c0001t0003g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+758C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638482 | |||||||
chr2:241638497 | T | A | 1 | a0001c0001t0001g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+773T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638497 | |||||||
chr2:241638498 | A | T | 1 | a0001c0001t0001g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+774A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638498 | |||||||
chr2:241638501 | T | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.10+777T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638501 | |||||||
chr2:241638535 | G | A | 143 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(140): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.10+811G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638535 | |||||||
chr2:241638555 | C | T | 6 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(3): Show |
8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+831C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638555 | |||||||
chr2:241638610 | T | A | 1 | a0001c0005t0002g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+886T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638610 | |||||||
chr2:241638705 | C | A | 11 | a0001c0002t0002g0018 a0001c0002t0002g0065 a0001c0002t0002g0068 others(8): Show |
12 | HG01952.hp2 HG01981.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.10+981C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638705 | |||||||
chr2:241638722 | A | G | 1 | a0002c0003t0004g0229 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.10+998A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638722 | |||||||
chr2:241638786 | C | T | 1 | a0001c0001t0019g0295 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.10+1062C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638786 | |||||||
chr2:241638935 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10+1211G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638935 | |||||||
chr2:241638982 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(2): Show |
6 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.10+1258C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638982 | |||||||
chr2:241638999 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10+1275C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638999 | |||||||
chr2:241639127 | G | T | 1 | a0001c0005t0002g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+1403G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639127 | |||||||
chr2:241639166 | C | T | 1 | a0001c0005t0002g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10+1442C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639166 | |||||||
chr2:241639174 | C | G | 144 | a0001c0001t0001g0225 a0001c0001t0003g0154 a0001c0001t0003g0159 others(141): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.10+1450C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639174 | |||||||
chr2:241639226 | C | T | 1 | a0002c0003t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.10+1502C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639226 | |||||||
chr2:241639230 | G | A | 7 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(4): Show |
10 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.10+1506G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639230 | |||||||
chr2:241639246 | A | G | 1 | a0001c0001t0003g0293 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.10+1522A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639246 | |||||||
chr2:241639335 | G | T | 144 | a0001c0001t0001g0225 a0001c0001t0003g0154 a0001c0001t0003g0159 others(141): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.10+1611G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639335 | |||||||
chr2:241639386 | A | C | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+1662A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639386 | |||||||
chr2:241639590 | G | C | 1 | a0001c0001t0003g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+1866G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639590 | |||||||
chr2:241639657 | G | T | 1 | a0001c0005t0002g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+1933G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639657 | |||||||
chr2:241639860 | G | T | 74 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(71): Show |
86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+2136G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639860 | |||||||
chr2:241639909 | G | A | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+2185G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639909 | |||||||
chr2:241639992 | C | G | 1 | a0001c0002t0002g0226 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10+2268C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639992 | |||||||
chr2:241640076 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.10+2352A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640076 | |||||||
chr2:241640242 | T | C | 231 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(228): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.10+2518T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640242 | |||||||
chr2:241640398 | C | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.10+2674C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640398 | |||||||
chr2:241640430 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.10+2706C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640430 | |||||||
chr2:241640432 | T | C | 1 | a0001c0002t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.10+2708T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640432 | |||||||
chr2:241640779 | A | G | 306 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(303): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.10+3055A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640779 | |||||||
chr2:241640787 | C | CG | 5 | a0001c0001t0001g0105 a0001c0002t0002g0136 a0001c0002t0012g0135 others(2): Show |
5 | HG02135.hp1 NA18959.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+3066dupG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241640787 | ||||||
chr2:241640818 | A | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.10+3094A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640818 | |||||||
chr2:241640836 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.10+3112C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640836 | |||||||
chr2:241640996 | A | G | 7 | a0001c0001t0005g0224 a0001c0001t0008g0035 a0001c0001t0008g0036 others(4): Show |
9 | HG02647.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.10+3272A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640996 | |||||||
chr2:241641055 | G | A | 183 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0003g0154 others(180): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.10+3331G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641055 | |||||||
chr2:241641057 | G | A | 29 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0003g0154 others(26): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.10+3333G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641057 | |||||||
chr2:241641201 | G | A | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.10+3477G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641201 | |||||||
chr2:241641317 | G | A | 106 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0162 others(103): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.10+3593G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641317 | |||||||
chr2:241641325 | C | G | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3601C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641325 | |||||||
chr2:241641325 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10+3601C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641325 | |||||||
chr2:241641326 | G | C | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3602G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641326 | |||||||
chr2:241641346 | C | T | 1 | a0001c0001t0003g0291 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.10+3622C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641346 | |||||||
chr2:241641411 | A | T | 1 | a0002c0003t0004g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10+3687A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641411 | |||||||
chr2:241641448 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.10+3724G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641448 | |||||||
chr2:241641448 | G | C | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3724G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641448 | |||||||
chr2:241641449 | C | G | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3725C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641449 | |||||||
chr2:241641458 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.10+3734G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641458 | |||||||
chr2:241641549 | C | CA | 15 | a0001c0001t0001g0107 a0001c0001t0001g0300 a0001c0001t0001g0301 others(12): Show |
16 | HG00639.hp1 HG02055.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.10+3842dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241641549 | ||||||
chr2:241641549 | C | CAA | 21 | a0001c0002t0002g0082 a0001c0005t0002g0090 a0001c0005t0002g0092 others(18): Show |
23 | HG01515.hp1 HG01884.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.10+3841_10+3842dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241641549 | ||||||
chr2:241641767 | G | A | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10+4043G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641767 | |||||||
chr2:241641951 | A | G | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+4227A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641951 | |||||||
chr2:241642033 | T | TA | 181 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(178): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.10+4319dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642033 | ||||||
chr2:241642109 | A | G | 1 | a0001c0010t0003g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10+4385A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642109 | |||||||
chr2:241642167 | G | GT | 6 | a0001c0001t0003g0296 a0001c0002t0002g0104 a0001c0002t0012g0135 others(3): Show |
6 | HG02135.hp1 HG03710.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.10+4456dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642167 | ||||||
chr2:241642173 | TTTTTTTT others(7): Show |
T | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+4451_10+4464del others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642173 | ||||||
chr2:241642188 | T | C | 307 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(304): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10+4464T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642188 | |||||||
chr2:241642336 | T | C | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.10+4612T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642336 | |||||||
chr2:241642393 | T | A | 74 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(71): Show |
86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+4669T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642393 | |||||||
chr2:241642411 | A | G | 1 | a0001c0001t0010g0211 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10+4687A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642411 | |||||||
chr2:241642495 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.10+4771G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642495 | |||||||
chr2:241642569 | G | GT | 263 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(260): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.10+4854dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642569 | ||||||
chr2:241642645 | A | C | 6 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(3): Show |
8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+4921A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642645 | |||||||
chr2:241642830 | CTAA | C | 76 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(73): Show |
88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+5107_10+5109del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642830 | |||||||
chr2:241642871 | C | CT | 80 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0237 others(77): Show |
89 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTT | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(39): Show |
49 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTT | 15 | a0001c0001t0001g0302 a0001c0001t0001g0313 a0001c0001t0001g0320 others(12): Show |
17 | HG00423.hp1 HG01243.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTT | 4 | a0001c0001t0001g0300 a0001c0002t0002g0072 a0001c0002t0002g0222 others(1): Show |
4 | HG02074.hp2 NA18984.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTT | 9 | a0001c0001t0017g0025 a0001c0002t0002g0004 a0001c0002t0002g0138 others(6): Show |
10 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(5): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTT | 56 | a0001c0001t0003g0159 a0001c0001t0003g0162 a0001c0001t0004g0032 others(53): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(6): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT | 27 | a0001c0001t0004g0032 a0001c0001t0004g0196 a0001c0002t0002g0002 others(24): Show |
30 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(7): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0004g0031 a0001c0001t0004g0199 a0001c0001t0005g0016 others(11): Show |
16 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0001t0004g0181 others(9): Show |
12 | HG01169.hp1 HG01433.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(9): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0002g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(11): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(13): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(11): Show |
3 | a0001c0002t0002g0027 a0001c0002t0002g0144 a0001c0002t0002g0156 |
4 | HG02132.hp2 NA18957.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(18): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(12): Show |
4 | a0001c0002t0002g0149 a0001c0002t0002g0226 a0001c0002t0012g0147 others(1): Show |
4 | HG00597.hp1 NA18969.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(19): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(13): Show |
2 | a0002c0003t0004g0140 a0002c0003t0004g0148 |
2 | HG02155.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(20): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(14): Show |
2 | a0001c0002t0002g0153 a0001c0002t0012g0135 |
2 | HG02135.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(21): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(15): Show |
3 | a0001c0002t0002g0139 a0001c0002t0021g0141 a0001c0002t0021g0151 |
3 | HG00438.hp1 HG02129.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(16): Show |
1 | a0001c0002t0002g0145 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(23): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(18): Show |
1 | a0001c0002t0012g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(25): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0154 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(26): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | CCTTTTTT others(2): Show |
C | 25 | a0001c0002t0002g0161 a0001c0005t0002g0090 a0001c0005t0002g0092 others(22): Show |
27 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.10+5148_10+5156del others(9): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642871 | CCTTTTTT others(3): Show |
C | 3 | a0001c0002t0002g0082 a0003c0004t0006g0096 a0003c0004t0023g0091 |
3 | HG01943.hp2 HG03041.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.10+5148_10+5157del others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | |||||||
chr2:241642872 | C | T | 274 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(271): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.10+5148C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642872 | |||||||
chr2:241642972 | T | C | 1 | a0001c0002t0002g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.10+5248T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642972 | |||||||
chr2:241643076 | G | A | 105 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0162 others(102): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10+5352G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643076 | |||||||
chr2:241643165 | GAACCACC others(6): Show |
G | 1 | a0003c0004t0026g0236 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.10+5446_10+5458del others(13): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643165 | ||||||
chr2:241643267 | C | T | 2 | a0001c0006t0002g0209 a0001c0006t0002g0210 |
2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.10+5543C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643267 | |||||||
chr2:241643310 | T | C | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+5586T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643310 | |||||||
chr2:241643364 | A | AT | 18 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(15): Show |
20 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.10+5662dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | ||||||
chr2:241643364 | A | ATT | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0042 others(30): Show |
38 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.10+5661_10+5662dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | ||||||
chr2:241643364 | A | ATTT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0302 a0001c0001t0001g0320 others(4): Show |
10 | HG00423.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.10+5660_10+5662dup others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | ||||||
chr2:241643364 | AT | A | 110 | a0001c0001t0001g0243 a0001c0001t0001g0325 a0001c0001t0003g0159 others(107): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.10+5662delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | ||||||
chr2:241643576 | A | G | 74 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(71): Show |
86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+5852A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643576 | |||||||
chr2:241643596 | A | G | 28 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(25): Show |
30 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.10+5872A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643596 | |||||||
chr2:241643603 | CAT | C | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.10+5887_10+5888del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643603 | ||||||
chr2:241643616 | A | G | 76 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(73): Show |
88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+5892A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643616 | |||||||
chr2:241643619 | T | G | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5895T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643619 | |||||||
chr2:241643663 | C | CGT | 139 | a0001c0001t0001g0130 a0001c0001t0003g0154 a0001c0001t0003g0159 others(136): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.10+5956_10+5957dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGT | 9 | a0001c0001t0003g0009 a0001c0001t0003g0246 a0001c0001t0004g0032 others(6): Show |
12 | HG00609.hp2 HG00639.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+5954_10+5957dup others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGTGT | 70 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.10+5952_10+5957dup others(6): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGTGTG others(1): Show |
10 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0284 others(7): Show |
11 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.10+5950_10+5957dup others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGTGTG others(3): Show |
26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(23): Show |
34 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.10+5948_10+5957dup others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGTGTG others(5): Show |
8 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0317 others(5): Show |
8 | HG00423.hp1 HG01891.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.10+5946_10+5957dup others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0001g0298 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10+5944_10+5957dup others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | CGT | C | 25 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(22): Show |
27 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.10+5956_10+5957del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643663 | CGTGT | C | 4 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5954_10+5957del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | ||||||
chr2:241643678 | G | GTGTGTGT others(3): Show |
6 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(3): Show |
8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+5957_10+5958ins others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643678 | ||||||
chr2:241643688 | A | T | 1 | a0002c0003t0007g0052 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.10+5964A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643688 | |||||||
chr2:241643690 | A | AT | 4 | a0001c0002t0002g0192 a0001c0002t0002g0193 a0002c0003t0007g0052 others(1): Show |
4 | HG00597.hp2 HG03834.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+5970dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643690 | ||||||
chr2:241643690 | AT | A | 8 | a0001c0001t0001g0109 a0001c0001t0005g0043 a0001c0001t0005g0327 others(5): Show |
10 | HG01099.hp1 HG02055.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.10+5970delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643690 | ||||||
chr2:241643692 | T | TCCCCCCC others(3): Show |
4 | a0001c0005t0002g0092 a0003c0004t0006g0019 a0003c0004t0006g0101 others(1): Show |
5 | HG02056.hp2 HG03041.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(4): Show |
4 | a0001c0005t0002g0064 a0001c0005t0002g0090 a0003c0004t0006g0088 others(1): Show |
4 | HG06807.hp1 NA18955.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(11): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(5): Show |
1 | a0003c0004t0009g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(7): Show |
5 | a0001c0002t0002g0082 a0001c0005t0002g0097 a0003c0004t0006g0083 others(2): Show |
5 | HG01515.hp1 HG01943.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(14): Show |
3 | a0003c0004t0006g0085 a0003c0004t0009g0084 a0003c0004t0009g0099 |
3 | HG02647.hp1 NA19030.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(21): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(15): Show |
1 | a0001c0006t0002g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | T | TCCCCCCC others(36): Show |
1 | a0003c0004t0026g0236 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(43): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643692 | TTTCC | T | 4 | a0003c0004t0009g0020 a0003c0004t0009g0021 a0003c0004t0009g0093 others(1): Show |
5 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.10+5969_10+5972del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | |||||||
chr2:241643693 | T | C | 23 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(20): Show |
24 | HG01496.hp2 HG01515.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.10+5969T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643693 | |||||||
chr2:241643694 | T | C | 29 | a0001c0001t0001g0116 a0001c0001t0001g0298 a0001c0001t0001g0299 others(26): Show |
30 | HG00738.hp2 HG01099.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.10+5970T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643694 | |||||||
chr2:241643694 | TC | T | 105 | a0001c0001t0003g0154 a0001c0001t0003g0160 a0001c0001t0004g0031 others(102): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.10+5981delC | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643694 | ||||||
chr2:241643694 | TCC | T | 77 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(74): Show |
89 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.10+5980_10+5981del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643694 | ||||||
chr2:241643695 | C | T | 46 | a0001c0001t0003g0159 a0001c0001t0003g0162 a0001c0001t0004g0032 others(43): Show |
58 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.10+5971C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643695 | |||||||
chr2:241643696 | C | T | 106 | a0001c0001t0003g0154 a0001c0001t0003g0160 a0001c0001t0004g0031 others(103): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.10+5972C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643696 | |||||||
chr2:241643699 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.10+5975C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643699 | |||||||
chr2:241643738 | C | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.10+6014C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643738 | |||||||
chr2:241643788 | C | G | 1 | a0001c0002t0012g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10+6064C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643788 | |||||||
chr2:241643812 | C | G | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+6088C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643812 | |||||||
chr2:241643843 | G | A | 4 | a0001c0002t0002g0034 a0001c0002t0002g0220 a0001c0002t0002g0221 others(1): Show |
5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+6119G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643843 | |||||||
chr2:241643879 | G | A | 73 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(70): Show |
85 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.10+6155G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643879 | |||||||
chr2:241643929 | A | C | 4 | a0001c0005t0002g0064 a0001c0005t0002g0090 a0001c0005t0002g0092 others(1): Show |
4 | NA18939.hp1 NA18954.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+6205A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643929 | |||||||
chr2:241643942 | C | T | 181 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(178): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6218C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643942 | |||||||
chr2:241643943 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0293 |
2 | HG00408.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.10+6219G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643943 | |||||||
chr2:241644045 | A | T | 181 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(178): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6321A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644045 | |||||||
chr2:241644138 | G | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.10+6414G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644138 | |||||||
chr2:241644241 | G | A | 1 | a0002c0003t0013g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10+6517G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644241 | |||||||
chr2:241644285 | G | A | 181 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(178): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6561G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644285 | |||||||
chr2:241644297 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+6573C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644297 | |||||||
chr2:241644314 | G | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.10+6590G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644314 | |||||||
chr2:241644350 | C | T | 1 | a0001c0001t0003g0009 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10+6626C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644350 | |||||||
chr2:241644360 | C | T | 1 | a0002c0003t0004g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.10+6636C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644360 | |||||||
chr2:241644363 | T | C | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+6639T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644363 | |||||||
chr2:241644537 | C | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(36): Show |
47 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.11-6473C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644537 | |||||||
chr2:241644538 | G | A | 3 | a0001c0001t0003g0162 a0001c0001t0005g0328 a0001c0001t0005g0329 |
3 | HG02486.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.11-6472G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644538 | |||||||
chr2:241644747 | C | T | 153 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(150): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.11-6263C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644747 | |||||||
chr2:241644864 | G | A | 1 | a0001c0002t0002g0076 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.11-6146G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644864 | |||||||
chr2:241644947 | C | CA | 99 | a0001c0001t0001g0111 a0001c0001t0003g0159 a0001c0001t0003g0160 others(96): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.11-6050dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241644947 | ||||||
chr2:241645028 | T | G | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11-5982T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645028 | |||||||
chr2:241645093 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.11-5917G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645093 | |||||||
chr2:241645218 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0024 others(16): Show |
25 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.11-5792C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645218 | |||||||
chr2:241645327 | G | C | 1 | a0006c0011t0006g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11-5683G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645327 | |||||||
chr2:241645335 | A | G | 28 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(25): Show |
30 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.11-5675A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645335 | |||||||
chr2:241645424 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11-5586A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645424 | |||||||
chr2:241645461 | T | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(43): Show |
56 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.11-5549T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645461 | |||||||
chr2:241645483 | C | T | 1 | a0002c0003t0041g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.11-5527C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645483 | |||||||
chr2:241645487 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-5523C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645487 | |||||||
chr2:241645505 | A | G | 149 | a0001c0001t0003g0154 a0001c0001t0003g0159 a0001c0001t0003g0160 others(146): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.11-5505A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645505 | |||||||
chr2:241645599 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-5411C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645599 | |||||||
chr2:241645626 | C | T | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.11-5384C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645626 | |||||||
chr2:241645729 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.11-5281C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645729 | |||||||
chr2:241645736 | CACAGT | C | 6 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(3): Show |
8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-5271_11-5267del others(5): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241645736 | ||||||
chr2:241645888 | A | G | 26 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(23): Show |
28 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.11-5122A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645888 | |||||||
chr2:241645940 | T | C | 1 | a0001c0002t0002g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.11-5070T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645940 | |||||||
chr2:241645954 | G | A | 37 | a0001c0001t0004g0169 a0001c0002t0002g0033 a0001c0002t0002g0158 others(34): Show |
47 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.11-5056G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645954 | |||||||
chr2:241645960 | C | T | 3 | a0001c0001t0037g0214 a0003c0008t0018g0048 a0003c0008t0018g0049 |
3 | HG03209.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.11-5050C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645960 | |||||||
chr2:241646201 | G | A | 229 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(226): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.11-4809G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646201 | |||||||
chr2:241646219 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(26): Show |
36 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.11-4791G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646219 | |||||||
chr2:241646306 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0304 a0001c0001t0001g0316 others(1): Show |
5 | HG01106.hp2 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.11-4704A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646306 | |||||||
chr2:241646319 | C | G | 2 | a0001c0007t0002g0073 a0001c0007t0002g0074 |
2 | NA18946.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.11-4691C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646319 | |||||||
chr2:241646394 | G | C | 1 | a0002c0003t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.11-4616G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646394 | |||||||
chr2:241646408 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.11-4602C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646408 | |||||||
chr2:241646461 | A | G | 1 | a0002c0003t0004g0023 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.11-4549A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646461 | |||||||
chr2:241646491 | C | A | 1 | a0001c0002t0002g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.11-4519C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646491 | |||||||
chr2:241646573 | C | T | 2 | a0001c0002t0002g0186 a0001c0002t0002g0197 |
2 | HG00609.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.11-4437C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646573 | |||||||
chr2:241646735 | A | G | 2 | a0002c0003t0004g0171 a0002c0003t0004g0172 |
2 | NA18954.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.11-4275A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646735 | |||||||
chr2:241646781 | C | CT | 7 | a0001c0001t0001g0107 a0001c0001t0001g0126 a0001c0001t0003g0234 others(4): Show |
8 | HG01928.hp2 HG01952.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-4210dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | ||||||
chr2:241646781 | CT | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(75): Show |
90 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.11-4210delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | ||||||
chr2:241646781 | CTT | C | 222 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(219): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.11-4211_11-4210del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | ||||||
chr2:241646837 | C | A | 1 | a0001c0001t0005g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.11-4173C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646837 | |||||||
chr2:241646845 | C | T | 3 | a0001c0001t0015g0212 a0001c0001t0015g0213 a0001c0001t0015g0215 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.11-4165C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646845 | |||||||
chr2:241647029 | C | G | 1 | a0001c0002t0002g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.11-3981C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647029 | |||||||
chr2:241647030 | C | T | 1 | a0002c0003t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.11-3980C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647030 | |||||||
chr2:241647075 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-3935T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647075 | |||||||
chr2:241647078 | C | T | 1 | a0003c0008t0018g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.11-3932C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647078 | |||||||
chr2:241647188 | G | C | 1 | a0003c0004t0009g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-3822G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647188 | |||||||
chr2:241647270 | CATG | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.11-3738_11-3736del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647270 | ||||||
chr2:241647297 | T | C | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-3713T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647297 | |||||||
chr2:241647357 | G | A | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-3653G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647357 | |||||||
chr2:241647389 | C | G | 1 | a0001c0001t0001g0286 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.11-3621C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647389 | |||||||
chr2:241647390 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.11-3620G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647390 | |||||||
chr2:241647423 | C | A | 10 | a0001c0002t0002g0029 a0001c0002t0002g0136 a0001c0002t0002g0173 others(7): Show |
11 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.11-3587C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647423 | |||||||
chr2:241647445 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11-3565C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647445 | |||||||
chr2:241647482 | G | A | 227 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(224): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.11-3528G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647482 | |||||||
chr2:241647622 | CA | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(75): Show |
92 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.11-3367delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | ||||||
chr2:241647622 | CAA | C | 213 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(210): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.11-3368_11-3367del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | ||||||
chr2:241647622 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0005g0327 a0001c0001t0005g0328 a0001c0001t0005g0329 others(2): Show |
6 | HG02055.hp1 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.11-3378_11-3367del others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | ||||||
chr2:241647639 | A | G | 179 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(176): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.11-3371A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647639 | |||||||
chr2:241647769 | G | C | 4 | a0001c0007t0002g0066 a0001c0007t0002g0067 a0001c0007t0002g0073 others(1): Show |
4 | HG02074.hp2 NA18946.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.11-3241G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647769 | |||||||
chr2:241647820 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.11-3190A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647820 | |||||||
chr2:241647836 | G | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(37): Show |
48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.11-3174G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647836 | |||||||
chr2:241647930 | A | G | 43 | a0001c0001t0003g0159 a0001c0001t0003g0162 a0001c0001t0004g0032 others(40): Show |
56 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.11-3080A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647930 | |||||||
chr2:241647941 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | NA18612.hp1 NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.11-3069C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647941 | |||||||
chr2:241648019 | C | T | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-2991C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648019 | |||||||
chr2:241648245 | C | A | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-2765C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648245 | |||||||
chr2:241648388 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.11-2622G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648388 | |||||||
chr2:241648427 | T | C | 1 | a0003c0004t0009g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-2583T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648427 | |||||||
chr2:241648594 | C | CA | 228 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(225): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.11-2404dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241648594 | ||||||
chr2:241648606 | A | G | 1 | a0003c0004t0026g0236 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.11-2404A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648606 | |||||||
chr2:241648607 | G | A | 1 | a0003c0004t0026g0236 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.11-2403G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648607 | |||||||
chr2:241648607 | G | GA | 26 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(23): Show |
28 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.11-2394dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241648607 | ||||||
chr2:241648616 | A | AG | 5 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(2): Show |
7 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.11-2394_11-2393ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648616 | |||||||
chr2:241648655 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.11-2355G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648655 | |||||||
chr2:241648838 | T | A | 180 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(177): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.11-2172T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648838 | |||||||
chr2:241648977 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.11-2033C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648977 | |||||||
chr2:241648999 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.11-2011T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648999 | |||||||
chr2:241649211 | T | C | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-1799T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649211 | |||||||
chr2:241649392 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-1618T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649392 | |||||||
chr2:241649403 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-1607T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649403 | |||||||
chr2:241649563 | C | A | 1 | a0001c0002t0002g0164 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.11-1447C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649563 | |||||||
chr2:241649603 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11-1407C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649603 | |||||||
chr2:241649759 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.11-1251T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649759 | |||||||
chr2:241649784 | C | CT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0107 a0001c0001t0001g0110 others(20): Show |
25 | HG00099.hp1 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.11-1210dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241649784 | ||||||
chr2:241650035 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.11-975C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650035 | |||||||
chr2:241650119 | C | T | 5 | a0001c0001t0003g0039 a0001c0001t0003g0246 a0001c0001t0003g0279 others(2): Show |
6 | HG00099.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.11-891C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650119 | |||||||
chr2:241650199 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0304 a0001c0001t0001g0315 others(3): Show |
7 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.11-811C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650199 | |||||||
chr2:241650225 | T | C | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.11-785T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650225 | |||||||
chr2:241650442 | G | T | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-568G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650442 | |||||||
chr2:241650446 | C | T | 182 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(179): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.11-564C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650446 | |||||||
chr2:241650630 | T | C | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.11-380T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650630 | |||||||
chr2:241650636 | C | T | 5 | a0003c0004t0006g0019 a0003c0004t0006g0086 a0003c0004t0006g0088 others(2): Show |
6 | HG02056.hp2 NA18959.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.11-374C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650636 | |||||||
chr2:241650637 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.11-373G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650637 | |||||||
chr2:241650639 | G | T | 10 | a0001c0002t0002g0002 a0001c0002t0002g0076 a0001c0002t0002g0077 others(7): Show |
14 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.11-371G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650639 | |||||||
chr2:241650684 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0304 a0001c0001t0001g0315 others(3): Show |
7 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.11-326A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650684 | |||||||
chr2:241650822 | T | C | 257 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(254): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.11-188T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650822 | |||||||
chr2:241650914 | G | A | 1 | a0001c0001t0005g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11-96G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650914 | |||||||
chr2:241650923 | A | G | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(43): Show |
56 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.11-87A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650923 | |||||||
chr2:241651251 | A | T | 1 | a0001c0001t0003g0277 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-13A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 2/12 | chr2 | 241651251 | |||||||
chr2:241651407 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.184+72A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651407 | |||||||
chr2:241651433 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184+98C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651433 | |||||||
chr2:241651652 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.184+317G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651652 | |||||||
chr2:241651658 | G | A | 1 | a0001c0002t0002g0142 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.184+323G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651658 | |||||||
chr2:241651811 | C | T | 1 | a0003c0004t0006g0088 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.184+476C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651811 | |||||||
chr2:241651813 | G | A | 1 | a0001c0001t0003g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.184+478G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651813 | |||||||
chr2:241651941 | C | T | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.184+606C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651941 | |||||||
chr2:241651992 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.184+657G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651992 | |||||||
chr2:241652013 | G | A | 6 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(3): Show |
8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.184+678G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652013 | |||||||
chr2:241652053 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184+718T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652053 | |||||||
chr2:241652118 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.184+783G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652118 | |||||||
chr2:241652126 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.184+791C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652126 | |||||||
chr2:241652173 | G | A | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.184+838G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652173 | |||||||
chr2:241652301 | C | T | 1 | a0003c0004t0009g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+966C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652301 | |||||||
chr2:241652559 | G | A | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-953G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652559 | |||||||
chr2:241652656 | C | G | 1 | a0001c0007t0002g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.185-856C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652656 | |||||||
chr2:241652691 | G | A | 1 | a0003c0004t0009g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.185-821G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652691 | |||||||
chr2:241652691 | G | T | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.185-821G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652691 | |||||||
chr2:241652895 | G | T | 5 | a0001c0002t0002g0138 a0001c0002t0002g0139 a0001c0002t0002g0152 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-617G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652895 | |||||||
chr2:241652932 | C | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.185-580C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652932 | |||||||
chr2:241652968 | A | G | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-544A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652968 | |||||||
chr2:241652989 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.185-523C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652989 | |||||||
chr2:241652999 | A | C | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-513A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652999 | |||||||
chr2:241653005 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.185-507C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653005 | |||||||
chr2:241653038 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-474C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653038 | |||||||
chr2:241653176 | A | G | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.185-336A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653176 | |||||||
chr2:241653221 | C | T | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.185-291C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653221 | |||||||
chr2:241653227 | G | A | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.185-285G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653227 | |||||||
chr2:241653407 | G | A | 1 | a0003c0004t0006g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185-105G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653407 | |||||||
chr2:241653506 | C | T | 1 | a0003c0008t0018g0049 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.185-6C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653506 | |||||||
chr2:241653644 | C | T | 1 | a0001c0001t0008g0036 | 2 | NA18971.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.283+34C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653644 | |||||||
chr2:241653678 | C | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283+68C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653678 | |||||||
chr2:241653699 | A | G | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(40): Show |
52 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.283+89A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653699 | |||||||
chr2:241653703 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.283+93G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653703 | |||||||
chr2:241653862 | C | T | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.283+252C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653862 | |||||||
chr2:241653947 | C | G | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.283+337C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653947 | |||||||
chr2:241653947 | C | T | 1 | a0001c0001t0038g0276 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+337C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653947 | |||||||
chr2:241653990 | G | GA | 47 | a0001c0001t0001g0126 a0001c0001t0003g0253 a0001c0001t0003g0254 others(44): Show |
57 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.283+401dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241653990 | ||||||
chr2:241653990 | GA | G | 37 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0124 others(34): Show |
38 | HG00323.hp2 HG01099.hp1 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.283+401delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241653990 | ||||||
chr2:241653992 | A | G | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+382A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653992 | |||||||
chr2:241654009 | A | AG | 5 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(2): Show |
7 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+399_283+400ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654009 | |||||||
chr2:241654009 | A | G | 5 | a0001c0001t0003g0133 a0001c0001t0003g0234 a0001c0001t0003g0235 others(2): Show |
5 | HG02074.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+399A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654009 | |||||||
chr2:241654009 | AAAG | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(23): Show |
31 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.283+411_283+413del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654009 | ||||||
chr2:241654010 | AAG | A | 8 | a0001c0001t0001g0007 a0001c0001t0005g0043 a0001c0001t0005g0327 others(5): Show |
11 | HG00642.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+402_283+403del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654010 | ||||||
chr2:241654014 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.283+404A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654014 | |||||||
chr2:241654148 | T | C | 1 | a0001c0001t0003g0305 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284-398T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654148 | |||||||
chr2:241654150 | T | C | 1 | a0001c0001t0003g0305 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284-396T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654150 | |||||||
chr2:241654160 | C | G | 1 | a0001c0001t0003g0283 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.284-386C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654160 | |||||||
chr2:241654160 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0225 |
3 | HG01168.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.284-386C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654160 | |||||||
chr2:241654252 | C | T | 1 | a0001c0001t0003g0271 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.284-294C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654252 | |||||||
chr2:241654264 | C | T | 126 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(123): Show |
143 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.284-282C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654264 | |||||||
chr2:241654282 | T | A | 1 | a0001c0005t0002g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.284-264T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654282 | |||||||
chr2:241654288 | A | G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(120): Show |
140 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.284-258A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654288 | |||||||
chr2:241654290 | A | G | 10 | a0001c0005t0002g0064 a0001c0005t0002g0090 a0001c0005t0002g0092 others(7): Show |
11 | HG02056.hp2 NA18939.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-256A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654290 | |||||||
chr2:241654376 | A | G | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.284-170A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654376 | |||||||
chr2:241654392 | T | G | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.284-154T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654392 | |||||||
chr2:241654419 | TA | T | 158 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0114 others(155): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.284-104delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | ||||||
chr2:241654419 | TAA | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(51): Show |
63 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.284-105_284-104del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | ||||||
chr2:241654419 | TAAA | T | 19 | a0001c0001t0001g0300 a0001c0001t0005g0327 a0001c0001t0005g0328 others(16): Show |
21 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-106_284-104del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | ||||||
chr2:241654419 | TAAAA | T | 38 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(35): Show |
41 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.284-107_284-104del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | ||||||
chr2:241654419 | TAAAAAAA | T | 16 | a0001c0005t0002g0090 a0001c0005t0002g0092 a0003c0004t0006g0019 others(13): Show |
18 | HG02056.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-110_284-104del others(7): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | ||||||
chr2:241654462 | A | G | 46 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(43): Show |
50 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-84A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654462 | |||||||
chr2:241654683 | G | A | 57 | a0001c0001t0003g0017 a0001c0001t0003g0038 a0001c0001t0003g0047 others(54): Show |
63 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.385+36G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654683 | |||||||
chr2:241654802 | C | T | 6 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0230 others(3): Show |
8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+155C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654802 | |||||||
chr2:241654811 | C | T | 31 | a0001c0001t0005g0206 a0001c0001t0010g0041 a0001c0001t0010g0308 others(28): Show |
34 | HG00642.hp1 HG01099.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.385+164C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654811 | |||||||
chr2:241654825 | C | T | 1 | a0001c0002t0002g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.385+178C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654825 | |||||||
chr2:241654860 | C | T | 79 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0237 others(76): Show |
90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.385+213C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654860 | |||||||
chr2:241655006 | C | T | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.386-265C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655006 | |||||||
chr2:241655093 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.386-178C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655093 | |||||||
chr2:241655095 | T | C | 67 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(64): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.386-176T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655095 | |||||||
chr2:241655207 | C | T | 100 | a0001c0001t0003g0159 a0001c0001t0003g0162 a0001c0001t0004g0031 others(97): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.386-64C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655207 | |||||||
chr2:241655483 | G | A | 1 | a0002c0003t0007g0055 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.458+140G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655483 | |||||||
chr2:241655597 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.458+254C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655597 | |||||||
chr2:241655789 | T | C | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+446T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655789 | |||||||
chr2:241655967 | C | T | 1 | a0001c0001t0010g0211 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.458+624C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655967 | |||||||
chr2:241656091 | G | T | 1 | a0001c0002t0002g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.458+748G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656091 | |||||||
chr2:241656136 | C | T | 2 | a0001c0002t0002g0018 a0001c0002t0002g0072 |
3 | NA18962.hp1 NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.458+793C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656136 | |||||||
chr2:241656171 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.458+828C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656171 | |||||||
chr2:241656199 | A | T | 182 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(179): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.458+856A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656199 | |||||||
chr2:241656295 | G | A | 6 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(3): Show |
8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.458+952G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656295 | |||||||
chr2:241656472 | C | A | 5 | a0001c0002t0002g0136 a0001c0002t0002g0173 a0001c0002t0002g0174 others(2): Show |
5 | NA18945.hp2 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+1129C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656472 | |||||||
chr2:241656505 | T | C | 190 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(187): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.458+1162T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656505 | |||||||
chr2:241656586 | C | T | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+1243C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656586 | |||||||
chr2:241656713 | G | A | 4 | a0001c0002t0002g0034 a0001c0002t0002g0220 a0001c0002t0002g0221 others(1): Show |
5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+1370G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656713 | |||||||
chr2:241656802 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.458+1459A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656802 | |||||||
chr2:241656981 | T | G | 1 | a0002c0003t0013g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458+1638T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656981 | |||||||
chr2:241657009 | CCTGGGCT others(13): Show |
C | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.458+1667_458+1686d others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657009 | |||||||
chr2:241657024 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(35): Show |
46 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.458+1681A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657024 | |||||||
chr2:241657028 | G | T | 1 | a0001c0001t0001g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.458+1685G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657028 | |||||||
chr2:241657056 | A | G | 303 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(300): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.458+1713A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657056 | |||||||
chr2:241657107 | C | G | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+1764C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657107 | |||||||
chr2:241657255 | G | A | 1 | a0001c0001t0003g0009 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.459-1853G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657255 | |||||||
chr2:241657290 | CT | C | 7 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0297 others(4): Show |
7 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-1804delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241657290 | ||||||
chr2:241657300 | T | TTG | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(35): Show |
46 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.459-1807_459-1806i others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241657300 | ||||||
chr2:241657392 | G | A | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.459-1716G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657392 | |||||||
chr2:241657458 | C | A | 1 | a0001c0002t0002g0164 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.459-1650C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657458 | |||||||
chr2:241657470 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(35): Show |
46 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.459-1638A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657470 | |||||||
chr2:241657497 | G | T | 1 | a0001c0001t0003g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.459-1611G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657497 | |||||||
chr2:241657580 | G | A | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459-1528G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657580 | |||||||
chr2:241657644 | C | A | 7 | a0001c0001t0005g0238 a0001c0001t0008g0035 a0001c0001t0008g0036 others(4): Show |
9 | HG03209.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-1464C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657644 | |||||||
chr2:241657884 | G | C | 68 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(65): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.459-1224G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657884 | |||||||
chr2:241657903 | G | C | 303 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(300): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.459-1205G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657903 | |||||||
chr2:241658139 | A | G | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(29): Show |
39 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.459-969A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658139 | |||||||
chr2:241658139 | A | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0304 a0001c0001t0001g0315 others(3): Show |
7 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-969A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658139 | |||||||
chr2:241658196 | C | T | 1 | a0001c0002t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.459-912C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658196 | |||||||
chr2:241658203 | G | T | 6 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(3): Show |
8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-905G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658203 | |||||||
chr2:241658482 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459-626T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658482 | |||||||
chr2:241658622 | T | TCACTGGC others(3): Show |
41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.459-482_459-473dup others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241658622 | ||||||
chr2:241658850 | A | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0107 others(9): Show |
16 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-258A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658850 | |||||||
chr2:241658852 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.459-256G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658852 | |||||||
chr2:241658860 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459-248C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658860 | |||||||
chr2:241658922 | A | C | 1 | a0001c0006t0002g0190 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459-186A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658922 | |||||||
chr2:241659002 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0005g0326 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.459-106C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659002 | |||||||
chr2:241659003 | G | A | 81 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(78): Show |
93 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.459-105G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659003 | |||||||
chr2:241659073 | A | T | 1 | a0001c0002t0002g0197 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.459-35A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659073 | |||||||
chr2:241659364 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+177C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659364 | |||||||
chr2:241659530 | C | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538+343C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659530 | |||||||
chr2:241659659 | C | T | 80 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(77): Show |
92 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.538+472C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659659 | |||||||
chr2:241659780 | T | C | 306 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(303): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.538+593T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659780 | |||||||
chr2:241659781 | T | C | 306 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(303): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.538+594T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659781 | |||||||
chr2:241659920 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.538+733G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659920 | |||||||
chr2:241659921 | G | T | 1 | a0002c0003t0004g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.538+734G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659921 | |||||||
chr2:241660062 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.538+875C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660062 | |||||||
chr2:241660112 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.538+925C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660112 | |||||||
chr2:241660146 | C | T | 2 | a0001c0002t0014g0030 a0001c0002t0014g0185 |
3 | HG01496.hp1 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.538+959C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660146 | |||||||
chr2:241660183 | C | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+996C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660183 | |||||||
chr2:241660232 | C | T | 7 | a0001c0001t0005g0238 a0001c0001t0008g0035 a0001c0001t0008g0036 others(4): Show |
9 | HG03209.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+1045C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660232 | |||||||
chr2:241660321 | C | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1134C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660321 | |||||||
chr2:241660354 | A | G | 342 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(339): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.538+1167A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660354 | |||||||
chr2:241660367 | C | G | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.538+1180C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660367 | |||||||
chr2:241660390 | G | A | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+1203G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660390 | |||||||
chr2:241660561 | T | C | 1 | a0002c0003t0004g0194 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.538+1374T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660561 | |||||||
chr2:241660703 | T | TA | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1517dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241660703 | ||||||
chr2:241660807 | C | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1620C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660807 | |||||||
chr2:241660941 | G | C | 1 | a0001c0001t0003g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.538+1754G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660941 | |||||||
chr2:241660968 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.538+1781C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660968 | |||||||
chr2:241661117 | G | A | 1 | a0006c0011t0006g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+1930G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661117 | |||||||
chr2:241661237 | C | G | 1 | a0001c0001t0001g0008 | 4 | HG01884.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+2050C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661237 | |||||||
chr2:241661284 | A | G | 1 | a0001c0001t0003g0267 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538+2097A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661284 | |||||||
chr2:241661430 | G | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538+2243G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661430 | |||||||
chr2:241661464 | G | A | 1 | a0003c0004t0009g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.538+2277G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661464 | |||||||
chr2:241661481 | C | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+2294C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661481 | |||||||
chr2:241661515 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.538+2328C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661515 | |||||||
chr2:241661573 | C | T | 1 | a0001c0002t0043g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2386C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661573 | |||||||
chr2:241661593 | G | T | 9 | a0001c0001t0005g0238 a0001c0001t0008g0035 a0001c0001t0008g0036 others(6): Show |
11 | HG03209.hp1 HG03209.hp2 NA18906.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+2406G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661593 | |||||||
chr2:241661643 | C | G | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.538+2456C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661643 | |||||||
chr2:241661653 | C | T | 1 | a0002c0003t0004g0194 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.538+2466C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661653 | |||||||
chr2:241661757 | C | T | 1 | a0002c0003t0004g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.538+2570C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661757 | |||||||
chr2:241661834 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.538+2647G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661834 | |||||||
chr2:241661871 | A | C | 1 | a0001c0010t0003g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.538+2684A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661871 | |||||||
chr2:241662013 | G | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(262): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.538+2826G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662013 | |||||||
chr2:241662098 | C | G | 1 | a0001c0001t0003g0267 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538+2911C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662098 | |||||||
chr2:241662199 | G | A | 185 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(182): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.538+3012G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662199 | |||||||
chr2:241662290 | G | C | 6 | a0001c0001t0005g0043 a0001c0001t0005g0327 a0001c0001t0005g0328 others(3): Show |
8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.538+3103G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662290 | |||||||
chr2:241662517 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.538+3330G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662517 | |||||||
chr2:241662553 | C | T | 1 | a0001c0001t0039g0262 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.538+3366C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662553 | |||||||
chr2:241662698 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.538+3511G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662698 | |||||||
chr2:241662740 | TGGGCCGG others(46): Show |
T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0144 a0001c0002t0002g0149 |
4 | NA18957.hp2 NA18975.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+3563_538+3615d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662740 | ||||||
chr2:241662751 | TGGTGGCT others(46): Show |
T | 1 | a0001c0002t0002g0153 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.538+3597_538+3649d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662751 | ||||||
chr2:241662761 | C | T | 238 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(235): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.538+3574C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662761 | |||||||
chr2:241662787 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.538+3600A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662787 | |||||||
chr2:241662798 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.538+3611C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662798 | |||||||
chr2:241662804 | C | T | 1 | a0001c0002t0002g0149 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.538+3617C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662804 | |||||||
chr2:241662855 | C | T | 1 | a0001c0001t0008g0036 | 2 | NA18971.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.538+3668C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662855 | |||||||
chr2:241662857 | CGGTGGCT others(46): Show |
C | 1 | a0001c0001t0003g0271 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.538+3703_539-3703d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662857 | ||||||
chr2:241662858 | G | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0331 |
3 | NA19006.hp1 NA19065.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.538+3671G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662858 | |||||||
chr2:241662952 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.539-3693C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662952 | |||||||
chr2:241662953 | G | A | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-3692G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662953 | |||||||
chr2:241662956 | C | CCGGGCG | 4 | a0001c0002t0002g0034 a0001c0002t0002g0220 a0001c0002t0002g0221 others(1): Show |
5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-3685_539-3680d others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662956 | ||||||
chr2:241663054 | C | T | 85 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0243 others(82): Show |
97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.539-3591C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663054 | |||||||
chr2:241663095 | T | G | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3550T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663095 | |||||||
chr2:241663097 | G | T | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3548G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663097 | |||||||
chr2:241663098 | T | G | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3547T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663098 | |||||||
chr2:241663125 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.539-3520C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663125 | |||||||
chr2:241663126 | G | A | 1 | a0001c0001t0032g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.539-3519G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663126 | |||||||
chr2:241663140 | C | T | 1 | a0001c0001t0003g0291 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.539-3505C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663140 | |||||||
chr2:241663175 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.539-3470G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663175 | |||||||
chr2:241663317 | G | C | 27 | a0001c0002t0002g0082 a0001c0005t0002g0064 a0001c0005t0002g0090 others(24): Show |
29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-3328G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663317 | |||||||
chr2:241663322 | C | A | 1 | a0002c0003t0004g0200 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.539-3323C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663322 | |||||||
chr2:241663374 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.539-3271G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663374 | |||||||
chr2:241663490 | G | C | 32 | a0001c0001t0003g0240 a0001c0002t0002g0082 a0001c0005t0002g0064 others(29): Show |
37 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-3155G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663490 | |||||||
chr2:241663567 | T | C | 1 | a0001c0001t0003g0260 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.539-3078T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663567 | |||||||
chr2:241663591 | T | C | 32 | a0001c0001t0003g0240 a0001c0002t0002g0082 a0001c0005t0002g0064 others(29): Show |
37 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-3054T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663591 | |||||||
chr2:241663794 | A | G | 3 | a0001c0002t0002g0082 a0003c0004t0006g0085 a0003c0004t0006g0087 |
3 | HG01515.hp1 HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.539-2851A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663794 | |||||||
chr2:241663811 | A | AT | 69 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0300 others(66): Show |
87 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.539-2818dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | ||||||
chr2:241663811 | A | ATT | 40 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(37): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.539-2819_539-2818d others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | ||||||
chr2:241663811 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0243 others(1): Show |
7 | HG01074.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-2818delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | ||||||
chr2:241663823 | T | G | 12 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0188 others(9): Show |
16 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-2822T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663823 | |||||||
chr2:241663829 | G | C | 13 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0188 others(10): Show |
17 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-2816G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663829 | |||||||
chr2:241663846 | C | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539-2799C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663846 | |||||||
chr2:241663895 | C | T | 1 | a0001c0002t0002g0157 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.539-2750C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663895 | |||||||
chr2:241663927 | A | G | 1 | a0001c0001t0003g0287 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.539-2718A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663927 | |||||||
chr2:241664025 | G | A | 2 | a0001c0001t0003g0258 a0001c0001t0003g0272 |
2 | NA18962.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.539-2620G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664025 | |||||||
chr2:241664039 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.539-2606T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664039 | |||||||
chr2:241664040 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01261.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.539-2605G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664040 | |||||||
chr2:241664138 | A | G | 1 | a0001c0002t0002g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.539-2507A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664138 | |||||||
chr2:241664164 | T | G | 38 | a0001c0001t0001g0314 a0001c0002t0002g0018 a0001c0002t0002g0026 others(35): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-2481T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664164 | |||||||
chr2:241664255 | A | G | 232 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(229): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.539-2390A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664255 | |||||||
chr2:241664279 | A | G | 3 | a0001c0001t0004g0031 a0001c0001t0004g0189 a0001c0001t0011g0031 |
3 | HG01099.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.539-2366A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664279 | |||||||
chr2:241664308 | T | G | 78 | a0001c0001t0001g0127 a0001c0001t0001g0243 a0001c0001t0001g0284 others(75): Show |
90 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.539-2337T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664308 | |||||||
chr2:241664318 | C | G | 1 | a0001c0002t0002g0050 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.539-2327C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664318 | |||||||
chr2:241664394 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.539-2251C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664394 | |||||||
chr2:241664459 | G | T | 3 | a0001c0002t0012g0135 a0001c0002t0012g0147 a0001c0002t0012g0155 |
3 | HG00597.hp1 HG00621.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.539-2186G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664459 | |||||||
chr2:241664471 | G | A | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-2174G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664471 | |||||||
chr2:241664596 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.539-2049A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664596 | |||||||
chr2:241664601 | C | T | 1 | a0001c0001t0008g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.539-2044C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664601 | |||||||
chr2:241664660 | C | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0009 others(90): Show |
110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.539-1985C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664660 | |||||||
chr2:241664729 | T | C | 1 | a0001c0002t0002g0183 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.539-1916T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664729 | |||||||
chr2:241664754 | A | G | 10 | a0001c0002t0002g0002 a0001c0002t0002g0076 a0001c0002t0002g0077 others(7): Show |
14 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-1891A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664754 | |||||||
chr2:241664825 | G | A | 160 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0009 others(157): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.539-1820G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664825 | |||||||
chr2:241664912 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539-1733C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664912 | |||||||
chr2:241664961 | A | G | 46 | a0001c0001t0003g0254 a0001c0001t0003g0256 a0001c0001t0003g0263 others(43): Show |
49 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.539-1684A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664961 | |||||||
chr2:241665039 | A | G | 42 | a0001c0001t0003g0265 a0001c0002t0002g0002 a0001c0002t0002g0004 others(39): Show |
52 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.539-1606A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665039 | |||||||
chr2:241665366 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-1279C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665366 | |||||||
chr2:241665391 | G | A | 13 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(10): Show |
16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-1254G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665391 | |||||||
chr2:241665466 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.539-1179T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665466 | |||||||
chr2:241665674 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
118 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.539-971G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665674 | |||||||
chr2:241665834 | T | C | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-811T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665834 | |||||||
chr2:241665835 | C | T | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-810C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665835 | |||||||
chr2:241665916 | A | G | 5 | a0003c0004t0006g0019 a0003c0004t0006g0086 a0003c0004t0006g0088 others(2): Show |
6 | HG02056.hp2 NA18959.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-729A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665916 | |||||||
chr2:241665947 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.539-698C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665947 | |||||||
chr2:241665947 | C | G | 2 | a0002c0003t0013g0045 a0002c0003t0013g0333 |
3 | HG00741.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.539-698C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665947 | |||||||
chr2:241666007 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.539-638G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666007 | |||||||
chr2:241666023 | T | A | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.539-622T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666023 | |||||||
chr2:241666109 | C | T | 13 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(10): Show |
16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-536C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666109 | |||||||
chr2:241666136 | C | T | 1 | a0001c0002t0014g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-509C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666136 | |||||||
chr2:241666231 | C | T | 88 | a0001c0001t0003g0242 a0001c0002t0002g0002 a0001c0002t0002g0004 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.539-414C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666231 | |||||||
chr2:241666260 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-385C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666260 | |||||||
chr2:241666261 | G | A | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-384G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666261 | |||||||
chr2:241666282 | G | T | 1 | a0001c0001t0019g0295 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.539-363G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666282 | |||||||
chr2:241666526 | T | C | 1 | a0001c0002t0002g0205 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.539-119T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666526 | |||||||
chr2:241666527 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0243 others(20): Show |
26 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.539-118G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666527 | |||||||
chr2:241666539 | C | T | 3 | a0001c0002t0002g0198 a0001c0006t0002g0209 a0001c0006t0002g0210 |
3 | HG01109.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.539-106C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666539 | |||||||
chr2:241666547 | C | T | 87 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(84): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.539-98C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666547 | |||||||
chr2:241666591 | G | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-54G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666591 | |||||||
chr2:241666593 | A | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-52A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666593 | |||||||
chr2:241666621 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.539-24G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666621 | |||||||
chr2:241666913 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.732+75G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666913 | |||||||
chr2:241666916 | G | A | 3 | a0001c0002t0002g0145 a0001c0002t0021g0141 a0001c0002t0021g0151 |
3 | HG00438.hp1 HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.732+78G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666916 | |||||||
chr2:241666925 | C | T | 1 | a0006c0011t0006g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.732+87C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666925 | |||||||
chr2:241666946 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.732+108G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666946 | |||||||
chr2:241666976 | C | T | 1 | a0001c0002t0024g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.732+138C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666976 | |||||||
chr2:241667096 | T | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.732+258T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667096 | |||||||
chr2:241667250 | C | T | 13 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(10): Show |
16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+412C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667250 | |||||||
chr2:241667268 | A | T | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.732+430A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667268 | |||||||
chr2:241667432 | T | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.732+594T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667432 | |||||||
chr2:241667450 | A | G | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.732+612A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667450 | |||||||
chr2:241667477 | G | A | 1 | a0003c0004t0009g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.732+639G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667477 | |||||||
chr2:241667493 | A | T | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-650A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667493 | |||||||
chr2:241667607 | TA | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(6): Show |
9 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-521delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 241667607 | ||||||
chr2:241667608 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
89 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.733-535A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667608 | |||||||
chr2:241667609 | A | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-534A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667609 | |||||||
chr2:241667683 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.733-460C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667683 | |||||||
chr2:241667684 | A | G | 21 | a0001c0002t0002g0026 a0001c0002t0002g0138 a0001c0002t0002g0139 others(18): Show |
21 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.733-459A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667684 | |||||||
chr2:241667895 | C | T | 21 | a0003c0004t0006g0019 a0003c0004t0006g0083 a0003c0004t0006g0085 others(18): Show |
23 | HG01099.hp1 HG01515.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-248C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667895 | |||||||
chr2:241668036 | T | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.733-107T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668036 | |||||||
chr2:241668068 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.733-75G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668068 | |||||||
chr2:241668069 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.733-74C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668069 | |||||||
chr2:241668091 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.733-52G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668091 | |||||||
chr2:241668348 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.811+127T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668348 | |||||||
chr2:241668363 | C | A | 3 | a0002c0003t0013g0045 a0002c0003t0013g0095 a0002c0003t0013g0333 |
4 | HG00741.hp1 HG01071.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+142C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668363 | |||||||
chr2:241668392 | G | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.812-148G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668392 | |||||||
chr2:241668509 | A | G | 88 | a0001c0001t0003g0162 a0001c0002t0002g0002 a0001c0002t0002g0004 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.812-31A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668509 | |||||||
chr2:241668700 | C | G | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.957+15C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668700 | |||||||
chr2:241668766 | G | GC | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+82dupC | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241668766 | ||||||
chr2:241668768 | G | GT | 50 | a0001c0001t0001g0307 a0001c0001t0003g0257 a0001c0001t0003g0289 others(47): Show |
60 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.957+93dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241668768 | ||||||
chr2:241668768 | G | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+83G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668768 | |||||||
chr2:241668777 | T | C | 2 | a0001c0001t0008g0232 a0001c0001t0008g0233 |
2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.957+92T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668777 | |||||||
chr2:241668789 | G | C | 22 | a0001c0001t0004g0179 a0001c0001t0005g0016 a0001c0001t0005g0043 others(19): Show |
28 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.957+104G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668789 | |||||||
chr2:241668872 | C | T | 1 | a0001c0002t0002g0175 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.957+187C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668872 | |||||||
chr2:241668898 | A | G | 1 | a0001c0001t0036g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.957+213A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668898 | |||||||
chr2:241668941 | G | A | 1 | a0001c0002t0002g0183 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.957+256G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668941 | |||||||
chr2:241668948 | G | A | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+263G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668948 | |||||||
chr2:241669018 | CACACGGG others(48): Show |
C | 79 | a0001c0001t0001g0008 a0001c0002t0002g0002 a0001c0002t0002g0004 others(76): Show |
95 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.957+359_957+413del others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669018 | ||||||
chr2:241669022 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(97): Show |
117 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.957+337C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669022 | |||||||
chr2:241669069 | T | C | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+384T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669069 | |||||||
chr2:241669100 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+415C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669100 | |||||||
chr2:241669123 | C | T | 1 | a0001c0002t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.957+438C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669123 | |||||||
chr2:241669124 | G | A | 2 | a0001c0001t0036g0249 a0003c0004t0009g0099 |
2 | HG00438.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.957+439G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669124 | |||||||
chr2:241669145 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.957+460C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669145 | |||||||
chr2:241669257 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0325 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.957+572G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669257 | |||||||
chr2:241669299 | G | A | 89 | a0001c0001t0001g0061 a0001c0002t0002g0002 a0001c0002t0002g0004 others(86): Show |
102 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.957+614G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669299 | |||||||
chr2:241669351 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+666C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669351 | |||||||
chr2:241669414 | G | A | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+729G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669414 | |||||||
chr2:241669504 | TTTTG | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.957+835_957+838del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669504 | ||||||
chr2:241669546 | C | T | 47 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0029 others(44): Show |
57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.957+861C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669546 | |||||||
chr2:241669568 | C | T | 22 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(19): Show |
29 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.957+883C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669568 | |||||||
chr2:241669569 | A | G | 303 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.957+884A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669569 | |||||||
chr2:241669622 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
120 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.957+937C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669622 | |||||||
chr2:241669632 | G | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+947G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669632 | |||||||
chr2:241669663 | A | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+978A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669663 | |||||||
chr2:241669679 | C | A | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+994C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669679 | |||||||
chr2:241669728 | T | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-998T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669728 | |||||||
chr2:241669743 | A | G | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-983A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669743 | |||||||
chr2:241669801 | G | A | 86 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(83): Show |
99 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.958-925G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669801 | |||||||
chr2:241669811 | G | T | 2 | a0001c0001t0003g0280 a0001c0001t0003g0281 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.958-915G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669811 | |||||||
chr2:241669837 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.958-889C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669837 | |||||||
chr2:241669850 | G | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(210): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.958-876G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669850 | |||||||
chr2:241669885 | A | G | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-841A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669885 | |||||||
chr2:241669908 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.958-818G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669908 | |||||||
chr2:241669913 | C | CT | 47 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0029 others(44): Show |
57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.958-812dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669913 | ||||||
chr2:241669946 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.958-780C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669946 | |||||||
chr2:241670021 | C | T | 87 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(84): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.958-705C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670021 | |||||||
chr2:241670089 | T | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-637T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670089 | |||||||
chr2:241670139 | C | T | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-587C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670139 | |||||||
chr2:241670140 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.958-586G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670140 | |||||||
chr2:241670171 | G | T | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.958-555G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670171 | |||||||
chr2:241670232 | G | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-494G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670232 | |||||||
chr2:241670245 | C | G | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-481C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670245 | |||||||
chr2:241670317 | C | T | 1 | a0002c0003t0042g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.958-409C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670317 | |||||||
chr2:241670318 | T | C | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.958-408T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670318 | |||||||
chr2:241670374 | C | T | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-352C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670374 | |||||||
chr2:241670424 | T | C | 1 | a0001c0001t0016g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.958-302T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670424 | |||||||
chr2:241670435 | C | T | 1 | a0001c0001t0003g0291 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.958-291C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670435 | |||||||
chr2:241670505 | G | A | 1 | a0002c0003t0004g0148 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.958-221G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670505 | |||||||
chr2:241670572 | G | A | 47 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0029 others(44): Show |
57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.958-154G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670572 | |||||||
chr2:241670577 | T | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-149T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670577 | |||||||
chr2:241670604 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.958-122A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670604 | |||||||
chr2:241670838 | T | C | 94 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(91): Show |
107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1014+56T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670838 | |||||||
chr2:241670925 | T | C | 1 | a0001c0001t0005g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1014+143T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670925 | |||||||
chr2:241670990 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1014+208C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670990 | |||||||
chr2:241671002 | G | A | 21 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(18): Show |
27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1014+220G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671002 | |||||||
chr2:241671087 | G | A | 3 | a0001c0001t0015g0212 a0001c0001t0015g0213 a0001c0001t0015g0215 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1015-225G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671087 | |||||||
chr2:241671087 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(189): Show |
225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015-225G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671087 | |||||||
chr2:241671092 | C | T | 1 | a0001c0002t0002g0222 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1015-220C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671092 | |||||||
chr2:241671225 | C | T | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1015-87C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671225 | |||||||
chr2:241671266 | A | G | 3 | a0001c0001t0015g0212 a0001c0001t0015g0213 a0001c0001t0015g0215 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1015-46A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671266 | |||||||
chr2:241671452 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1108+47T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671452 | |||||||
chr2:241671464 | C | T | 3 | a0002c0003t0013g0045 a0002c0003t0013g0095 a0002c0003t0013g0333 |
4 | HG00741.hp1 HG01071.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+59C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671464 | |||||||
chr2:241671635 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1108+230C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671635 | |||||||
chr2:241671640 | G | A | 21 | a0001c0001t0005g0016 a0001c0001t0005g0043 a0001c0001t0005g0178 others(18): Show |
27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1108+235G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671640 | |||||||
chr2:241671655 | G | A | 3 | a0003c0004t0009g0099 a0003c0004t0009g0100 a0003c0004t0034g0103 |
3 | HG02647.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1108+250G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671655 | |||||||
chr2:241671752 | C | G | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1108+347C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671752 | |||||||
chr2:241671762 | G | C | 1 | a0003c0004t0034g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1108+357G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671762 | |||||||
chr2:241671817 | G | A | 1 | a0001c0001t0017g0025 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1109-374G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671817 | |||||||
chr2:241671842 | C | T | 1 | a0001c0001t0003g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1109-349C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671842 | |||||||
chr2:241671857 | T | C | 88 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(85): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1109-334T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671857 | |||||||
chr2:241671872 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
123 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1109-319G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671872 | |||||||
chr2:241671911 | T | G | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0325 |
3 | HG02451.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1109-280T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671911 | |||||||
chr2:241671934 | G | C | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-257G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671934 | |||||||
chr2:241671959 | A | G | 41 | a0001c0002t0002g0018 a0001c0002t0002g0026 a0001c0002t0002g0027 others(38): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1109-232A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671959 | |||||||
chr2:241671963 | T | C | 1 | a0001c0002t0002g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1109-228T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671963 | |||||||
chr2:241671994 | C | G | 2 | a0003c0008t0018g0048 a0003c0008t0018g0049 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-197C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671994 | |||||||
chr2:241672132 | G | A | 86 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0018 others(83): Show |
98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1109-59G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241672132 | |||||||
chr2:241672136 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1109-55C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241672136 |