Item | Value |
---|---|
geneid | 9776 |
ensemblid | ENSG00000175224.17 |
hgncid | 29091 |
symbol | ATG13 |
name | autophagy related 13 |
refseq_nuc | NM_001346311.2 |
refseq_prot | NP_001333240.1 |
ensembl_nuc | ENST00000683050.1 |
ensembl_prot | ENSP00000507809.1 |
mane_status | MANE Select |
chr | chr11 |
start | 46617553 |
end | 46674518 |
strand | + |
ver | v1.2 |
region | chr11:46617553-46674518 |
region5000 | chr11:46612553-46679518 |
regionname0 | ATG13_chr11_46617553_46674518 |
regionname5000 | ATG13_chr11_46612553_46679518 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 550 | 216 | 85 | 46 | 54 | 10 | 19 | 36 | ATG13_chr11_46612553_46679518 | ATG13 | METDL others(545): Show |
chr11 | 46612553 | 46679518 |
a0002 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | METDL others(545): Show |
chr11 | 46612553 | 46679518 |
a0003 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | METDL others(545): Show |
chr11 | 46612553 | 46679518 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1650 | 204 | 77 | 45 | 53 | 10 | 17 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0001c0002 | 0/0 | 1650 | 7 | 6 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0001c0003 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0001c0004 | 0/0 | 1650 | 2 | 0 | 0 | 0 | 0 | 2 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0001c0006 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0002c0005 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 | ||
a0003c0007 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | ATGGA others(1645): Show |
chr11 | 46612553 | 46679518 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4244 | 103 | 43 | 28 | 18 | 8 | 6 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0002 | 0/0 | 4244 | 36 | 8 | 11 | 10 | 1 | 6 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0003 | 0/1 | 4244 | 23 | 0 | 3 | 16 | 0 | 3 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0004 | 0/0 | 4244 | 14 | 14 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0006 | 0/0 | 4244 | 5 | 0 | 0 | 5 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0007 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0008 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0009 | 0/0 | 4244 | 3 | 2 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0010 | 0/0 | 4244 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0011 | 1/0 | 4246 | 2 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4241): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0012 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0013 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0014 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0015 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0016 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0017 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0018 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0019 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0022 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0001t0023 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0002t0005 | 0/0 | 4244 | 5 | 5 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0002t0020 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0002t0021 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0003t0005 | 0/0 | 4244 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0004t0001 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0001c0006t0003 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0002c0005t0001 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
a0003c0007t0001 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | GGCCA others(4239): Show |
chr11 | 46612553 | 46679518 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0007g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0009g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0010g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0010g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0011g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0013g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0016g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0018g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0022g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0001t0023g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0020g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0002t0021g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0003t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0001c0006t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0002c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
a0003c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0087 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01099 | hp2 | a0001 | c0001 | t0010 | g0089 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01109 | hp1 | a0001 | c0002 | t0021 | g0031 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0029 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01516 | hp1 | a0001 | c0001 | t0018 | g0088 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CDX | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02280 | hp1 | a0001 | c0002 | t0005 | g0208 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02615 | hp2 | a0001 | c0003 | t0005 | g0206 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02818 | hp2 | a0001 | c0002 | t0005 | g0204 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02965 | hp2 | a0001 | c0002 | t0020 | g0030 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02976 | hp1 | a0001 | c0001 | t0019 | g0028 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0097 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03453 | hp2 | a0001 | c0003 | t0005 | g0205 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0207 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03654 | hp1 | a0001 | c0001 | t0022 | g0159 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG04115 | hp1 | a0001 | c0001 | t0013 | g0058 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG04115 | hp2 | a0001 | c0004 | t0001 | g0171 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | CHB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18940 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18971 | hp1 | a0001 | c0001 | t0017 | g0168 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18978 | hp2 | a0001 | c0001 | t0015 | g0079 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19056 | hp1 | a0001 | c0001 | t0023 | g0100 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19090 | hp2 | a0001 | c0006 | t0003 | g0178 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA19240 | hp2 | a0001 | c0002 | t0005 | g0210 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0170 | SAS | GIH | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20905 | hp2 | a0002 | c0005 | t0001 | g0099 | SAS | GIH | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0067 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0080 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | USA | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
NA21309 | hp2 | a0003 | c0007 | t0001 | g0143 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0151 | REF | REF | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0130 | REF | REF | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46650250 | A | G | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.391A>G | p.Ile131Val | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/19 | 798/4246 | 391/1653 | 131/550 | chr11 | 46650250 | |||
chr11:46668863 | G | A | 1 | a0002 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1399G>A | p.Gly467Arg | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/19 | 1806/4246 | 1399/1653 | 467/550 | chr11 | 46668863 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46645398 | T | A | 1 | a0001c0003 | 2 | HG02615.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.129T>A | p.Ser43Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 4/19 | 536/4246 | 129/1653 | 43/550 | chr11 | 46645398 | |||
chr11:46657599 | T | C | 1 | a0001c0004 | 2 | HG04115.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.672T>C | p.Ser224Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/19 | 1079/4246 | 672/1653 | 224/550 | chr11 | 46657599 | |||
chr11:46667788 | C | T | 1 | a0001c0006 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.1152C>T | p.Thr384Thr | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/19 | 1559/4246 | 1152/1653 | 384/550 | chr11 | 46667788 | |||
chr11:46667803 | T | C | 2 | a0001c0002 a0001c0003 |
9 | HG01109.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.1167T>C | p.Ser389Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/19 | 1574/4246 | 1167/1653 | 389/550 | chr11 | 46667803 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46617598 | C | T | 1 | a0001c0001t0023 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-362C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | 26694 | chr11 | 46617598 | ||||||
chr11:46617641 | T | C | 1 | a0001c0001t0010 | 2 | HG01069.hp2 HG01099.hp2 |
5_prime_UTR_variant | MODIFIER | c.-319T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | 26651 | chr11 | 46617641 | ||||||
chr11:46617694 | C | T | 1 | a0001c0001t0022 | 1 | HG03654.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-266C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | chr11 | 46617694 | |||||||
chr11:46672522 | G | A | 1 | a0001c0001t0006 | 5 | HG00597.hp1 HG02040.hp2 HG02132.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*190G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 190 | chr11 | 46672522 | ||||||
chr11:46672628 | C | T | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0019 others(2): Show |
20 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 296 | chr11 | 46672628 | ||||||
chr11:46672763 | GTC | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*432_*433delTC | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 432 | chr11 | 46672763 | ||||||
chr11:46672867 | C | T | 1 | a0001c0001t0009 | 3 | HG01243.hp1 HG01884.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 535 | chr11 | 46672867 | ||||||
chr11:46672946 | C | A | 1 | a0001c0001t0007 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*614C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 614 | chr11 | 46672946 | ||||||
chr11:46673008 | T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 676 | chr11 | 46673008 | ||||||
chr11:46673048 | T | C | 1 | a0001c0001t0012 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 716 | chr11 | 46673048 | ||||||
chr11:46673385 | C | T | 1 | a0001c0002t0021 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1053 | chr11 | 46673385 | ||||||
chr11:46673386 | G | A | 1 | a0001c0001t0013 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1054 | chr11 | 46673386 | ||||||
chr11:46673815 | C | T | 1 | a0001c0001t0008 | 3 | HG02280.hp2 NA19043.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1483 | chr11 | 46673815 | ||||||
chr11:46673864 | T | C | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
93 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1532T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1532 | chr11 | 46673864 | ||||||
chr11:46673871 | C | T | 1 | a0001c0001t0016 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1539 | chr11 | 46673871 | ||||||
chr11:46673933 | G | A | 3 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0014 |
38 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1601G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1601 | chr11 | 46673933 | ||||||
chr11:46673947 | G | A | 1 | a0001c0001t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1615G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1615 | chr11 | 46673947 | ||||||
chr11:46674001 | G | A | 1 | a0001c0001t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1669G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1669 | chr11 | 46674001 | ||||||
chr11:46674167 | A | G | 2 | a0001c0002t0005 a0001c0003t0005 |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1835A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1835 | chr11 | 46674167 | ||||||
chr11:46674278 | G | A | 2 | a0001c0002t0020 a0001c0002t0021 |
2 | HG01109.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1946 | chr11 | 46674278 | ||||||
chr11:46674335 | A | G | 1 | a0001c0001t0015 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2003 | chr11 | 46674335 | ||||||
chr11:46674373 | G | A | 1 | a0001c0001t0017 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2041G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2041 | chr11 | 46674373 | ||||||
chr11:46674431 | A | T | 1 | a0001c0001t0018 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2099 | chr11 | 46674431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46617973 | G | T | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+83G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46617973 | |||||||
chr11:46618032 | G | A | 67 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(64): Show |
69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-70+142G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618032 | |||||||
chr11:46618208 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-70+318G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618208 | |||||||
chr11:46618253 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-70+363C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618253 | |||||||
chr11:46618408 | C | G | 1 | a0001c0001t0003g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-70+518C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618408 | |||||||
chr11:46618468 | T | G | 2 | a0001c0001t0007g0004 a0001c0001t0007g0067 |
3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+578T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618468 | |||||||
chr11:46618517 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-70+627A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618517 | |||||||
chr11:46618753 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
5 | HG02451.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+863T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618753 | |||||||
chr11:46618764 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-70+874C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618764 | |||||||
chr11:46618953 | A | G | 65 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(62): Show |
67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-70+1063A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618953 | |||||||
chr11:46619035 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-70+1145G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619035 | |||||||
chr11:46619222 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-70+1332A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619222 | |||||||
chr11:46619372 | C | CT | 29 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(26): Show |
29 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-70+1511dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | C | CTTTTTT | 10 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0035 others(7): Show |
10 | HG02451.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+1506_-70+1511d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | C | CTTTTTTT | 4 | a0001c0001t0004g0003 a0001c0001t0004g0043 a0001c0001t0004g0045 others(1): Show |
5 | HG02258.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+1505_-70+1511d others(9): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(7): Show |
10 | HG01257.hp1 HG01515.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+1503_-70+1511d others(11): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | C | CTTTTTTT others(3): Show |
9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0059 others(6): Show |
9 | HG00735.hp1 HG01074.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+1502_-70+1511d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-70+1499_-70+1511d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | CT | C | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+1511delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+1501_-70+1511d others(13): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619372 | CTTTTTTT others(5): Show |
C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(14): Show |
18 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-70+1500_-70+1511d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | ||||||
chr11:46619439 | C | T | 2 | a0001c0004t0001g0170 a0001c0004t0001g0171 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-70+1549C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619439 | |||||||
chr11:46619556 | G | T | 1 | a0001c0001t0003g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-70+1666G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619556 | |||||||
chr11:46619638 | T | A | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+1748T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619638 | |||||||
chr11:46619753 | G | A | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-70+1863G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619753 | |||||||
chr11:46619866 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-70+1976A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619866 | |||||||
chr11:46619901 | C | T | 1 | a0001c0001t0017g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-70+2011C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619901 | |||||||
chr11:46619969 | C | CA | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+2080dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619969 | ||||||
chr11:46619985 | C | T | 2 | a0001c0004t0001g0170 a0001c0004t0001g0171 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-70+2095C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619985 | |||||||
chr11:46620012 | G | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2122G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620012 | |||||||
chr11:46620013 | C | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2123C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620013 | |||||||
chr11:46620026 | C | CA | 6 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0172 others(3): Show |
6 | HG01192.hp1 HG01981.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+2154dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46620026 | ||||||
chr11:46620026 | CA | C | 78 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0001g0160 others(75): Show |
80 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-70+2154delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46620026 | ||||||
chr11:46620035 | A | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-70+2145A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620035 | |||||||
chr11:46620104 | T | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(52): Show |
57 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-70+2214T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620104 | |||||||
chr11:46620159 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0197 |
3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-70+2269C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620159 | |||||||
chr11:46620161 | G | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2271G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620161 | |||||||
chr11:46620256 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+2366G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620256 | |||||||
chr11:46620385 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+2495G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620385 | |||||||
chr11:46620550 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00609.hp1 HG02040.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+2660C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620550 | |||||||
chr11:46620551 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
11 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-70+2661G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620551 | |||||||
chr11:46620644 | G | A | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-70+2754G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620644 | |||||||
chr11:46620752 | G | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2862G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620752 | |||||||
chr11:46620896 | A | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0164 |
2 | HG01496.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-70+3006A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620896 | |||||||
chr11:46621099 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0070 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-70+3209C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621099 | |||||||
chr11:46621221 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-70+3331G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621221 | |||||||
chr11:46621302 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-70+3412C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621302 | |||||||
chr11:46621355 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-70+3465A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621355 | |||||||
chr11:46621363 | T | A | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3473T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621363 | |||||||
chr11:46621692 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3802A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621692 | |||||||
chr11:46621757 | A | G | 1 | a0001c0001t0011g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-70+3867A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621757 | |||||||
chr11:46621766 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3876A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621766 | |||||||
chr11:46621849 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-70+3959C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621849 | |||||||
chr11:46622073 | TTACATAT others(13): Show |
T | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+4186_-70+4205d others(22): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622073 | ||||||
chr11:46622076 | C | CAT | 8 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0156 others(5): Show |
8 | HG00438.hp1 HG00673.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4237_-70+4238d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | C | CATAT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0152 a0001c0001t0001g0155 others(3): Show |
6 | HG00140.hp1 HG00673.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+4235_-70+4238d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | C | CATATATA others(5): Show |
1 | a0001c0001t0003g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-70+4227_-70+4238d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CAT | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01993.hp1 HG02040.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+4237_-70+4238d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATAT | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0106 others(12): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-70+4235_-70+4238d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATAT | C | 12 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0114 others(9): Show |
12 | HG00438.hp2 HG01358.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.-70+4233_-70+4238d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(1): Show |
C | 21 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(18): Show |
21 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-70+4231_-70+4238d others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(3): Show |
C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0081 others(11): Show |
14 | HG00642.hp2 HG01070.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70+4229_-70+4238d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(5): Show |
C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0139 a0001c0001t0001g0154 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4227_-70+4238d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(7): Show |
C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0077 others(7): Show |
10 | HG01516.hp1 HG02165.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+4225_-70+4238d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(9): Show |
C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00738.hp2 HG02559.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+4223_-70+4238d others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(11): Show |
C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0110 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+4221_-70+4238d others(20): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(13): Show |
C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0135 others(2): Show |
5 | HG01261.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+4219_-70+4238d others(22): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(15): Show |
C | 1 | a0001c0001t0004g0043 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-70+4217_-70+4238d others(24): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(17): Show |
C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0085 others(18): Show |
22 | HG00099.hp2 HG01123.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-70+4215_-70+4238d others(26): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(19): Show |
C | 46 | a0001c0001t0001g0116 a0001c0001t0001g0190 a0001c0001t0001g0191 others(43): Show |
47 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70+4213_-70+4238d others(28): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622076 | CATATATA others(23): Show |
C | 2 | a0001c0001t0003g0076 a0001c0001t0003g0102 |
2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-70+4209_-70+4238d others(32): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | ||||||
chr11:46622092 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-70+4202T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622092 | |||||||
chr11:46622119 | A | T | 1 | a0001c0001t0003g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-70+4229A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622119 | |||||||
chr11:46622120 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-70+4231_-70+4246d others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622120 | |||||||
chr11:46622122 | TATATATT others(7): Show |
T | 1 | a0001c0001t0003g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-70+4233_-70+4246d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622122 | |||||||
chr11:46622123 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-70+4233A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622123 | |||||||
chr11:46622123 | ATATATT | A | 2 | a0001c0001t0001g0104 a0001c0001t0003g0108 |
2 | HG00099.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.-70+4237_-70+4242d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622123 | ||||||
chr11:46622125 | A | ATATT | 3 | a0001c0001t0001g0148 a0001c0001t0015g0079 a0001c0003t0005g0206 |
3 | HG01884.hp1 HG02615.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-70+4241_-70+4244d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622125 | ||||||
chr11:46622125 | A | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(10): Show |
14 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70+4235A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622125 | |||||||
chr11:46622129 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-70+4239T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622129 | |||||||
chr11:46622136 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-70+4246A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622136 | |||||||
chr11:46622512 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-70+4622A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622512 | |||||||
chr11:46622530 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-70+4640A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622530 | |||||||
chr11:46622593 | T | G | 65 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(62): Show |
67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-70+4703T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622593 | |||||||
chr11:46623070 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5180G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623070 | |||||||
chr11:46623083 | G | A | 1 | a0001c0001t0008g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-70+5193G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623083 | |||||||
chr11:46623265 | G | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-70+5375G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623265 | |||||||
chr11:46623273 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+5383A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623273 | |||||||
chr11:46623293 | C | CAAAGA | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+5412_-70+5416d others(7): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46623293 | ||||||
chr11:46623563 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-70+5673G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623563 | |||||||
chr11:46624008 | G | T | 1 | a0001c0001t0002g0025 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-69-6037G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624008 | |||||||
chr11:46624010 | A | AT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-6021dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624010 | ||||||
chr11:46624108 | G | A | 1 | a0001c0001t0008g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-69-5937G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624108 | |||||||
chr11:46624224 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-69-5821G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624224 | |||||||
chr11:46624480 | A | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(64): Show |
69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-69-5565A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624480 | |||||||
chr11:46624487 | G | C | 1 | a0001c0001t0011g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-69-5558G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624487 | |||||||
chr11:46624488 | A | AT | 9 | a0001c0001t0001g0093 a0001c0001t0001g0145 a0001c0001t0001g0146 others(6): Show |
9 | HG01106.hp2 HG01109.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-69-5544dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624488 | ||||||
chr11:46624488 | AT | A | 4 | a0001c0001t0004g0003 a0001c0001t0004g0034 a0001c0001t0004g0035 others(1): Show |
5 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-5544delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624488 | ||||||
chr11:46624499 | T | TG | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-5546_-69-5545i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624499 | |||||||
chr11:46624837 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-69-5208A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624837 | |||||||
chr11:46624883 | A | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-69-5162A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624883 | |||||||
chr11:46625074 | T | C | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-69-4971T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625074 | |||||||
chr11:46625269 | C | CT | 26 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0135 others(23): Show |
28 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-69-4752dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | ||||||
chr11:46625269 | C | CTT | 5 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0172 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-4753_-69-4752d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | ||||||
chr11:46625269 | CT | C | 47 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(44): Show |
48 | HG00642.hp1 HG00642.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-69-4752delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | ||||||
chr11:46625332 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-4713A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625332 | |||||||
chr11:46625351 | C | A | 1 | a0001c0003t0005g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-69-4694C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625351 | |||||||
chr11:46625732 | C | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-69-4313C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625732 | |||||||
chr11:46625793 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-69-4252G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625793 | |||||||
chr11:46626425 | T | C | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-3620T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626425 | |||||||
chr11:46626540 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-69-3505G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626540 | |||||||
chr11:46626882 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(96): Show |
105 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(102): Show |
intron_variant | MODIFIER | c.-69-3163G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626882 | |||||||
chr11:46627026 | G | A | 1 | a0001c0001t0014g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-69-3019G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627026 | |||||||
chr11:46627109 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
11 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-2936G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627109 | |||||||
chr11:46627287 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-2758A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627287 | |||||||
chr11:46627358 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-69-2687G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627358 | |||||||
chr11:46627385 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
23 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-2660T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627385 | |||||||
chr11:46628082 | C | CA | 26 | a0001c0001t0001g0078 a0001c0001t0001g0141 a0001c0001t0001g0161 others(23): Show |
27 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-69-1944dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628082 | ||||||
chr11:46628082 | CA | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0155 others(2): Show |
5 | HG01496.hp1 HG01515.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-1944delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628082 | ||||||
chr11:46628169 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
12 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.-69-1876G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628169 | |||||||
chr11:46628211 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-1834T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628211 | |||||||
chr11:46628369 | T | C | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1676T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628369 | |||||||
chr11:46628424 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-69-1621G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628424 | |||||||
chr11:46628508 | A | G | 1 | a0001c0001t0012g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-69-1537A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628508 | |||||||
chr11:46628523 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-1522C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628523 | |||||||
chr11:46628786 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-1259T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628786 | |||||||
chr11:46628825 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-69-1220C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628825 | |||||||
chr11:46628888 | T | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(64): Show |
69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-69-1157T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628888 | |||||||
chr11:46628938 | CT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
151 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-69-1092delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628938 | ||||||
chr11:46629004 | G | A | 1 | a0003c0007t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-69-1041G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629004 | |||||||
chr11:46629305 | G | C | 1 | a0001c0002t0020g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-69-740G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629305 | |||||||
chr11:46629842 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-69-203G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629842 | |||||||
chr11:46629902 | C | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-69-143C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629902 | |||||||
chr11:46630222 | T | C | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14+122T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630222 | |||||||
chr11:46630514 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+414C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630514 | |||||||
chr11:46630568 | C | CTTTT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(94): Show |
103 | HG00609.hp1 HG00735.hp1 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.-14+482_-14+485dup others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46630568 | ||||||
chr11:46630568 | C | CTTTTT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0084 others(17): Show |
21 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14+481_-14+485dup others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46630568 | ||||||
chr11:46630768 | A | G | 1 | a0001c0001t0019g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+668A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630768 | |||||||
chr11:46630902 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14+802G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630902 | |||||||
chr11:46631032 | A | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(52): Show |
57 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14+932A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46631032 | |||||||
chr11:46631192 | G | T | 12 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0002g0050 others(9): Show |
12 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14+1092G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46631192 | |||||||
chr11:46632127 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0173 |
2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-14+2027G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632127 | |||||||
chr11:46632597 | C | T | 1 | a0001c0002t0005g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-14+2497C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632597 | |||||||
chr11:46632688 | CTT | C | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2591_-14+2592d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46632688 | ||||||
chr11:46632854 | T | C | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+2754T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632854 | |||||||
chr11:46632995 | T | TAA | 16 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(13): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+2903_-14+2904d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46632995 | ||||||
chr11:46633001 | A | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG01981.hp1 NA18942.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+2901A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633001 | |||||||
chr11:46633003 | A | AAT | 5 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0182 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+2926_-14+2927d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633003 | ||||||
chr11:46633003 | A | T | 34 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0141 others(31): Show |
35 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-14+2903A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633003 | |||||||
chr11:46633005 | T | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0071 others(45): Show |
51 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.-14+2905T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633005 | |||||||
chr11:46633007 | T | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0091 others(22): Show |
28 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14+2907T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633007 | |||||||
chr11:46633009 | T | A | 5 | a0001c0001t0001g0200 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2909T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633009 | |||||||
chr11:46633011 | T | A | 1 | a0001c0003t0005g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-14+2911T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633011 | |||||||
chr11:46633015 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+2916_-14+2926d others(13): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633015 | |||||||
chr11:46633016 | ATATATAT others(6): Show |
A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0135 a0001c0001t0001g0136 others(17): Show |
22 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14+2918_-14+2930d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633016 | ||||||
chr11:46633026 | A | AT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0070 others(5): Show |
9 | HG01496.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+2941dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633026 | ||||||
chr11:46633026 | A | ATAT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
19 | HG00735.hp1 HG01257.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633026 | ||||||
chr11:46633026 | A | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0104 a0001c0001t0001g0105 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14+2926A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633026 | |||||||
chr11:46633027 | T | TA | 2 | a0001c0001t0001g0069 a0001c0001t0002g0012 |
2 | HG02818.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633027 | |||||||
chr11:46633027 | T | TATA | 14 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(11): Show |
15 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633027 | |||||||
chr11:46633028 | T | A | 65 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-14+2928T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633028 | |||||||
chr11:46633029 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14+2929T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633029 | |||||||
chr11:46633030 | T | A | 5 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2930T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633030 | |||||||
chr11:46633051 | G | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+2951G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633051 | |||||||
chr11:46633129 | A | G | 1 | a0001c0001t0004g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+3029A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633129 | |||||||
chr11:46633348 | T | C | 1 | a0001c0002t0020g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-14+3248T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633348 | |||||||
chr11:46633370 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+3270C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633370 | |||||||
chr11:46633537 | G | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14+3437G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633537 | |||||||
chr11:46633774 | A | C | 1 | a0001c0001t0004g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+3674A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633774 | |||||||
chr11:46633777 | C | T | 1 | a0001c0001t0008g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+3677C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633777 | |||||||
chr11:46633830 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14+3730C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633830 | |||||||
chr11:46634062 | A | AT | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+3963dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634062 | ||||||
chr11:46634092 | G | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0057 |
3 | HG02886.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14+3992G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634092 | |||||||
chr11:46634265 | T | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14+4165T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634265 | |||||||
chr11:46634318 | G | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+4218G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634318 | |||||||
chr11:46634359 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-14+4259A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634359 | |||||||
chr11:46634407 | CT | C | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4320delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634407 | ||||||
chr11:46634411 | T | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+4311T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634411 | |||||||
chr11:46634474 | C | G | 1 | a0001c0001t0008g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+4374C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634474 | |||||||
chr11:46634502 | G | GTCC | 65 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(62): Show |
67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-14+4404_-14+4406d others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634502 | ||||||
chr11:46634687 | G | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+4587G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634687 | |||||||
chr11:46634875 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0197 |
3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-14+4775G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634875 | |||||||
chr11:46634900 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00609.hp1 HG02040.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+4800A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634900 | |||||||
chr11:46634947 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+4847C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634947 | |||||||
chr11:46635195 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14+5095C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635195 | |||||||
chr11:46635454 | C | A | 2 | a0001c0004t0001g0170 a0001c0004t0001g0171 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14+5354C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635454 | |||||||
chr11:46635459 | T | G | 1 | a0001c0001t0004g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-14+5359T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635459 | |||||||
chr11:46635727 | C | T | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5627C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635727 | |||||||
chr11:46635871 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+5771T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635871 | |||||||
chr11:46635880 | T | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
134 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(131): Show |
intron_variant | MODIFIER | c.-14+5780T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635880 | |||||||
chr11:46636055 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14+5955G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636055 | |||||||
chr11:46636384 | C | T | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+6284C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636384 | |||||||
chr11:46636518 | A | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+6418A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636518 | |||||||
chr11:46636557 | C | CA | 51 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0085 others(48): Show |
53 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-14+6481dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | ||||||
chr11:46636557 | C | CAA | 10 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0002g0015 others(7): Show |
10 | HG00735.hp1 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+6480_-14+6481d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | ||||||
chr11:46636557 | CA | C | 12 | a0001c0001t0004g0003 a0001c0001t0004g0034 a0001c0001t0004g0035 others(9): Show |
13 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+6481delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | ||||||
chr11:46636810 | C | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+6710C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636810 | |||||||
chr11:46637016 | T | G | 1 | a0001c0001t0003g0102 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-14+6916T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637016 | |||||||
chr11:46637163 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+7063G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637163 | |||||||
chr11:46637176 | A | T | 7 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0127 others(4): Show |
7 | HG00438.hp1 HG01993.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+7076A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637176 | |||||||
chr11:46637328 | A | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13-6951A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637328 | |||||||
chr11:46638041 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-13-6238G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638041 | |||||||
chr11:46638129 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-13-6150T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638129 | |||||||
chr11:46638602 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-13-5677C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638602 | |||||||
chr11:46638620 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-5659A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638620 | |||||||
chr11:46638841 | T | C | 1 | a0001c0001t0003g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-13-5438T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638841 | |||||||
chr11:46638888 | A | C | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-5391A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638888 | |||||||
chr11:46638902 | G | A | 1 | a0001c0001t0019g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-5377G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638902 | |||||||
chr11:46638920 | A | C | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0063 |
3 | HG02145.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-5359A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638920 | |||||||
chr11:46638991 | TA | T | 2 | a0001c0002t0005g0207 a0001c0002t0005g0208 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13-5287delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638991 | |||||||
chr11:46638994 | T | A | 2 | a0001c0002t0005g0207 a0001c0002t0005g0208 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13-5285T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638994 | |||||||
chr11:46638995 | TA | T | 5 | a0001c0002t0005g0204 a0001c0002t0005g0209 a0001c0002t0005g0210 others(2): Show |
5 | HG02615.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5283delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638995 | |||||||
chr11:46638996 | A | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0066 others(24): Show |
29 | HG00673.hp1 HG01069.hp1 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-5283A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638996 | |||||||
chr11:46639000 | T | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-13-5279T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639000 | |||||||
chr11:46639073 | T | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(45): Show |
49 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.-13-5206T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639073 | |||||||
chr11:46639074 | G | A | 1 | a0001c0002t0021g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13-5205G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639074 | |||||||
chr11:46639099 | T | C | 1 | a0001c0001t0011g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13-5180T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639099 | |||||||
chr11:46639189 | T | C | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-5090T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639189 | |||||||
chr11:46639374 | T | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4905T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639374 | |||||||
chr11:46639853 | A | AT | 6 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0188 others(3): Show |
6 | HG00609.hp1 NA18940.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-4406dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | ||||||
chr11:46639853 | AT | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0085 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-4406delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | ||||||
chr11:46639853 | ATT | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(20): Show |
25 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13-4407_-13-4406d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | ||||||
chr11:46639911 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13-4368T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639911 | |||||||
chr11:46639986 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4293T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639986 | |||||||
chr11:46640567 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-13-3712G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640567 | |||||||
chr11:46640610 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-13-3669C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640610 | |||||||
chr11:46640939 | G | T | 7 | a0001c0001t0004g0003 a0001c0001t0004g0034 a0001c0001t0004g0035 others(4): Show |
8 | HG02647.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-3340G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640939 | |||||||
chr11:46641003 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-13-3276C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641003 | |||||||
chr11:46641279 | C | A | 3 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0057 |
3 | HG02886.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-13-3000C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641279 | |||||||
chr11:46641297 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13-2982C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641297 | |||||||
chr11:46641662 | G | T | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-2617G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641662 | |||||||
chr11:46641760 | A | AT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-13-2505dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641760 | ||||||
chr11:46641760 | A | ATT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-2506_-13-2505d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641760 | ||||||
chr11:46641780 | CAG | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0160 a0001c0001t0001g0162 |
3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-13-2496_-13-2495d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641780 | ||||||
chr11:46641888 | C | A | 15 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0001t0001g0158 others(12): Show |
15 | HG00609.hp1 HG00673.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-2391C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641888 | |||||||
chr11:46641951 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-2328T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641951 | |||||||
chr11:46641972 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-13-2307G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641972 | |||||||
chr11:46642076 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-2203G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642076 | |||||||
chr11:46642081 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0182 |
3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-13-2198C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642081 | |||||||
chr11:46642304 | G | GT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0073 others(91): Show |
97 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-13-1955dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | ||||||
chr11:46642304 | G | GTT | 20 | a0001c0001t0001g0077 a0001c0001t0001g0124 a0001c0001t0001g0141 others(17): Show |
20 | HG00609.hp1 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-1956_-13-1955d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | ||||||
chr11:46642304 | GT | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
15 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-1955delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | ||||||
chr11:46642304 | GTTTTTTT others(2): Show |
G | 37 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(34): Show |
38 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-13-1963_-13-1955d others(11): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | ||||||
chr11:46642366 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-1913C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642366 | |||||||
chr11:46642370 | A | G | 1 | a0001c0001t0008g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-1909A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642370 | |||||||
chr11:46643068 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13-1211C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643068 | |||||||
chr11:46643412 | C | CT | 4 | a0001c0001t0003g0133 a0001c0001t0003g0189 a0001c0001t0003g0193 others(1): Show |
4 | HG00597.hp2 NA18983.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-866dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46643412 | ||||||
chr11:46643511 | C | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13-768C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643511 | |||||||
chr11:46643523 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13-756G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643523 | |||||||
chr11:46643552 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13-727G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643552 | |||||||
chr11:46643612 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
17 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-649dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46643612 | ||||||
chr11:46643631 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-13-648A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643631 | |||||||
chr11:46643645 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-634C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643645 | |||||||
chr11:46643716 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-563A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643716 | |||||||
chr11:46643980 | A | G | 1 | a0001c0001t0012g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-299A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643980 | |||||||
chr11:46644249 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-30A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46644249 | |||||||
chr11:46644542 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0003g0120 |
3 | HG00558.hp1 HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.69+182A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644542 | |||||||
chr11:46644585 | A | AT | 34 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(31): Show |
35 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.69+239dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 46644585 | ||||||
chr11:46644585 | A | T | 1 | a0001c0001t0014g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+225A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644585 | |||||||
chr11:46644586 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.69+226T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644586 | |||||||
chr11:46644721 | T | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.69+361T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644721 | |||||||
chr11:46645114 | A | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.70-225A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46645114 | |||||||
chr11:46645255 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.70-84A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46645255 | |||||||
chr11:46645518 | T | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150+99T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 4/18 | chr11 | 46645518 | |||||||
chr11:46646211 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0181 |
2 | HG00738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.270+222C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646211 | |||||||
chr11:46646217 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+228C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646217 | |||||||
chr11:46646391 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0066 others(8): Show |
13 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.270+402G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646391 | |||||||
chr11:46646457 | TTTTTTG | T | 81 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(78): Show |
82 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.270+487_270+492del others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46646457 | ||||||
chr11:46646845 | G | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+856G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646845 | |||||||
chr11:46646965 | G | T | 1 | a0001c0001t0003g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.270+976G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646965 | |||||||
chr11:46647271 | GTTTTTTT others(6): Show |
G | 87 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(84): Show |
88 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.270+1305_270+1317d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647271 | ||||||
chr11:46647280 | G | GT | 52 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(49): Show |
54 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.270+1303dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647280 | ||||||
chr11:46647280 | G | T | 1 | a0001c0001t0004g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+1291G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647280 | |||||||
chr11:46647280 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+1303_270+1316d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647280 | ||||||
chr11:46647283 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0118 |
2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.270+1294T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647283 | |||||||
chr11:46647288 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0010g0087 a0001c0001t0010g0089 |
3 | HG01069.hp1 HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.270+1299T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647288 | |||||||
chr11:46647293 | G | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.270+1304G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647293 | |||||||
chr11:46647633 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-1504G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647633 | |||||||
chr11:46647702 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.271-1435A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647702 | |||||||
chr11:46648107 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.271-1030C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648107 | |||||||
chr11:46648159 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271-978G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648159 | |||||||
chr11:46648495 | T | TGTCAACC others(3): Show |
1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-642_271-641ins others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648495 | |||||||
chr11:46648502 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-635G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648502 | |||||||
chr11:46648504 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-633C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648504 | |||||||
chr11:46648512 | C | T | 1 | a0001c0001t0006g0180 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-625C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648512 | |||||||
chr11:46648513 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-624T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648513 | |||||||
chr11:46648514 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-623T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648514 | |||||||
chr11:46648516 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-621C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648516 | |||||||
chr11:46648517 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-620G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648517 | |||||||
chr11:46648519 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-618C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648519 | |||||||
chr11:46648523 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-614A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648523 | |||||||
chr11:46648558 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-579C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648558 | |||||||
chr11:46648559 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-578A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648559 | |||||||
chr11:46648560 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-577C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648560 | |||||||
chr11:46648611 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-526A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648611 | |||||||
chr11:46648658 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.271-479T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648658 | |||||||
chr11:46648777 | T | TA | 15 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(12): Show |
16 | HG00597.hp2 HG00609.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-338dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46648777 | ||||||
chr11:46648777 | TA | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0002g0019 others(10): Show |
13 | HG01515.hp2 HG02040.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.271-338delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46648777 | ||||||
chr11:46648798 | A | G | 1 | a0001c0001t0002g0020 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.271-339A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648798 | |||||||
chr11:46648901 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0145 |
2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.271-236G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648901 | |||||||
chr11:46649306 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+123A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649306 | |||||||
chr11:46649307 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0197 |
3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.317+124T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649307 | |||||||
chr11:46649484 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.317+301C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649484 | |||||||
chr11:46649535 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.317+352C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649535 | |||||||
chr11:46649843 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
9 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.318-334C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649843 | |||||||
chr11:46650136 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.318-41G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46650136 | |||||||
chr11:46650513 | C | T | 2 | a0001c0001t0006g0185 a0001c0001t0006g0186 |
2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.458+196C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650513 | |||||||
chr11:46650524 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.458+207T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650524 | |||||||
chr11:46650699 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+382G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650699 | |||||||
chr11:46650812 | G | A | 15 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0001t0001g0158 others(12): Show |
15 | HG00609.hp1 HG00673.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.458+495G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650812 | |||||||
chr11:46650826 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+509G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650826 | |||||||
chr11:46650950 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.458+633A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650950 | |||||||
chr11:46651092 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.458+775T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651092 | |||||||
chr11:46651369 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.458+1052A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651369 | |||||||
chr11:46651504 | T | C | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+1187T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651504 | |||||||
chr11:46651543 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.458+1226A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651543 | |||||||
chr11:46651608 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.458+1291A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651608 | |||||||
chr11:46651630 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.458+1313A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651630 | |||||||
chr11:46651762 | C | A | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+1445C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651762 | |||||||
chr11:46651794 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(64): Show |
69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.458+1477C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651794 | |||||||
chr11:46652216 | C | G | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.458+1899C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652216 | |||||||
chr11:46652679 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.458+2362C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652679 | |||||||
chr11:46652720 | T | C | 5 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG01074.hp2 HG01261.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+2403T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652720 | |||||||
chr11:46652915 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.458+2598G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652915 | |||||||
chr11:46653180 | C | CT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
9 | HG02257.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.458+2880dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46653180 | ||||||
chr11:46653236 | G | A | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.458+2919G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653236 | |||||||
chr11:46653267 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0016g0080 |
2 | HG01192.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.458+2950G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653267 | |||||||
chr11:46653404 | C | A | 1 | a0001c0001t0003g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.459-2829C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653404 | |||||||
chr11:46653417 | G | T | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459-2816G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653417 | |||||||
chr11:46653426 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2807G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653426 | |||||||
chr11:46653480 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.459-2753C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653480 | |||||||
chr11:46653576 | T | G | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459-2657T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653576 | |||||||
chr11:46653577 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459-2656T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653577 | |||||||
chr11:46653578 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459-2655T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653578 | |||||||
chr11:46653580 | TG | T | 2 | a0001c0001t0001g0122 a0001c0001t0003g0117 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.459-2652delG | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653580 | |||||||
chr11:46653805 | A | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2428A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653805 | |||||||
chr11:46653868 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-2365G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653868 | |||||||
chr11:46653883 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0065 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.459-2350A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653883 | |||||||
chr11:46654010 | T | C | 1 | a0001c0001t0012g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-2223T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654010 | |||||||
chr11:46654266 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459-1967C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654266 | |||||||
chr11:46654281 | T | TTA | 17 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0018 others(14): Show |
17 | HG02280.hp1 HG02615.hp1 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATA | 11 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0013 others(8): Show |
12 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATA | 11 | a0001c0001t0002g0010 a0001c0001t0002g0017 a0001c0001t0002g0056 others(8): Show |
11 | HG01261.hp1 HG02451.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(1): Show |
5 | a0001c0001t0002g0047 a0001c0001t0002g0052 a0001c0001t0002g0061 others(2): Show |
5 | HG01074.hp2 HG01515.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(3): Show |
2 | a0001c0001t0004g0003 a0001c0002t0005g0209 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459-1951_459-1950i others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(9): Show |
1 | a0001c0001t0004g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(11): Show |
1 | a0001c0001t0004g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(20): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(15): Show |
4 | a0001c0001t0004g0003 a0001c0001t0004g0038 a0001c0001t0004g0039 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(24): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(17): Show |
4 | a0001c0001t0004g0036 a0001c0001t0004g0045 a0001c0001t0009g0027 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(26): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(19): Show |
1 | a0001c0001t0009g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(28): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654281 | T | TTATATAT others(23): Show |
1 | a0001c0001t0004g0034 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-1951_459-1950i others(32): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | ||||||
chr11:46654283 | T | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(57): Show |
62 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.459-1950T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654283 | |||||||
chr11:46654283 | T | TTA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
23 | HG00609.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.459-1924_459-1923d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | ||||||
chr11:46654283 | T | TTATA | 19 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0081 others(16): Show |
20 | HG00099.hp1 HG00099.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.459-1926_459-1923d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | ||||||
chr11:46654283 | T | TTATATA | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG00609.hp1 HG02040.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-1928_459-1923d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | ||||||
chr11:46654283 | T | TTATATAT others(3): Show |
1 | a0001c0004t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.459-1932_459-1923d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | ||||||
chr11:46654283 | TTA | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0011g0068 |
3 | HG01515.hp1 HG02451.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.459-1924_459-1923d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | ||||||
chr11:46654325 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459-1908C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654325 | |||||||
chr11:46654807 | C | T | 84 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-1426C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654807 | |||||||
chr11:46654866 | C | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0017 others(2): Show |
5 | NA18960.hp2 NA18978.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1367C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654866 | |||||||
chr11:46655125 | C | T | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.459-1108C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655125 | |||||||
chr11:46655141 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.459-1092T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655141 | |||||||
chr11:46655260 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01261.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-973G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655260 | |||||||
chr11:46655315 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0182 |
3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.459-918A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655315 | |||||||
chr11:46655616 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.459-617A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655616 | |||||||
chr11:46655790 | T | C | 1 | a0001c0001t0006g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.459-443T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655790 | |||||||
chr11:46656184 | C | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0001g0160 others(10): Show |
13 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-49C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46656184 | |||||||
chr11:46656314 | T | TCTCCTAA others(9): Show |
1 | a0001c0001t0001g0134 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.499+42_499+57dupCT others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656314 | ||||||
chr11:46656624 | C | G | 1 | a0001c0002t0005g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.499+351C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656624 | |||||||
chr11:46656742 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.500-353G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656742 | |||||||
chr11:46656773 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500-322G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656773 | |||||||
chr11:46656862 | A | G | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-233A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656862 | |||||||
chr11:46656912 | C | CACACAT | 56 | a0001c0001t0001g0134 a0001c0001t0002g0002 a0001c0001t0002g0010 others(53): Show |
58 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.500-178_500-173dup others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656912 | ||||||
chr11:46656922 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.500-173C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656922 | |||||||
chr11:46656928 | T | TAC | 2 | a0001c0001t0001g0153 a0001c0001t0003g0126 |
2 | HG01123.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.500-147_500-146dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656928 | ||||||
chr11:46656928 | TAC | T | 17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-147_500-146del others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656928 | ||||||
chr11:46657322 | T | C | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+131T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657322 | |||||||
chr11:46657412 | T | G | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.597-112T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657412 | |||||||
chr11:46657431 | G | A | 1 | a0001c0001t0011g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597-93G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657431 | |||||||
chr11:46657765 | A | G | 1 | a0001c0002t0005g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.695+143A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46657765 | |||||||
chr11:46657939 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+317C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46657939 | |||||||
chr11:46658021 | A | G | 1 | a0001c0001t0014g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.695+399A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658021 | |||||||
chr11:46658389 | C | T | 1 | a0001c0002t0005g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.695+767C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658389 | |||||||
chr11:46658453 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.695+831T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658453 | |||||||
chr11:46658479 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.695+857C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658479 | |||||||
chr11:46658533 | C | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.696-859C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658533 | |||||||
chr11:46658638 | C | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0001g0160 others(10): Show |
13 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-754C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658638 | |||||||
chr11:46658895 | G | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.696-497G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658895 | |||||||
chr11:46659164 | C | G | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-228C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46659164 | |||||||
chr11:46659676 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.789+191C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659676 | |||||||
chr11:46659806 | A | G | 1 | a0001c0002t0005g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789+321A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659806 | |||||||
chr11:46659865 | A | C | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.789+380A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659865 | |||||||
chr11:46659952 | T | A | 1 | a0001c0001t0003g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.789+467T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659952 | |||||||
chr11:46660149 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.789+664C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660149 | |||||||
chr11:46660386 | G | GT | 137 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(134): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.789+915dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | ||||||
chr11:46660386 | G | GTT | 5 | a0001c0001t0001g0081 a0001c0001t0001g0118 a0001c0001t0001g0188 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+914_789+915dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | ||||||
chr11:46660386 | GT | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+915delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | ||||||
chr11:46660667 | C | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.789+1182C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660667 | |||||||
chr11:46660704 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0003g0189 |
2 | HG03239.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.789+1219G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660704 | |||||||
chr11:46660723 | A | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0203 |
3 | HG01106.hp1 HG02257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.789+1238A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660723 | |||||||
chr11:46660882 | T | A | 1 | a0001c0001t0003g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.789+1397T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660882 | |||||||
chr11:46661006 | A | G | 2 | a0001c0001t0004g0037 a0001c0001t0004g0040 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.789+1521A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661006 | |||||||
chr11:46661035 | T | A | 1 | a0001c0001t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+1550T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661035 | |||||||
chr11:46661215 | A | G | 1 | a0001c0001t0004g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.789+1730A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661215 | |||||||
chr11:46661243 | C | T | 1 | a0001c0001t0003g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.789+1758C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661243 | |||||||
chr11:46661390 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.789+1905C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661390 | |||||||
chr11:46661517 | C | CA | 68 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.789+2050dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46661517 | ||||||
chr11:46661517 | CA | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
21 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.789+2050delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46661517 | ||||||
chr11:46661570 | G | A | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+2085G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661570 | |||||||
chr11:46661622 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.789+2137A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661622 | |||||||
chr11:46662034 | C | CAT | 3 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0182 |
3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.790-1960_790-1959d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46662034 | ||||||
chr11:46662034 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.790-1963C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662034 | |||||||
chr11:46662045 | A | C | 3 | a0001c0001t0009g0027 a0001c0001t0009g0029 a0001c0001t0009g0044 |
3 | HG01243.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.790-1952A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662045 | |||||||
chr11:46662075 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.790-1922G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662075 | |||||||
chr11:46662130 | C | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1867C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662130 | |||||||
chr11:46662134 | C | CA | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1863_790-1862i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662134 | |||||||
chr11:46662407 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.790-1590A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662407 | |||||||
chr11:46662419 | A | G | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.790-1578A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662419 | |||||||
chr11:46662532 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.790-1465T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662532 | |||||||
chr11:46662974 | A | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.790-1023A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662974 | |||||||
chr11:46663070 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.790-927C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663070 | |||||||
chr11:46663127 | T | G | 65 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(62): Show |
67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.790-870T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663127 | |||||||
chr11:46663221 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0124 |
2 | HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.790-776G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663221 | |||||||
chr11:46663265 | C | CA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.790-710dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | ||||||
chr11:46663265 | C | CAA | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0081 others(16): Show |
19 | HG00673.hp2 HG01099.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.790-711_790-710dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | ||||||
chr11:46663265 | CAAAAAA | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-715_790-710del others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | ||||||
chr11:46663289 | G | A | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-708G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663289 | |||||||
chr11:46663426 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0160 a0001c0001t0001g0162 |
3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.790-571C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663426 | |||||||
chr11:46663945 | C | CT | 18 | a0001c0001t0001g0083 a0001c0001t0001g0121 a0001c0001t0001g0156 others(15): Show |
18 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.790-34dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663945 | ||||||
chr11:46664555 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.889-294A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 12/18 | chr11 | 46664555 | |||||||
chr11:46664710 | G | A | 84 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.889-139G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 12/18 | chr11 | 46664710 | |||||||
chr11:46665053 | C | G | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+94C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 13/18 | chr11 | 46665053 | |||||||
chr11:46665317 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1000-66G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 13/18 | chr11 | 46665317 | |||||||
chr11:46665677 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1136+158C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46665677 | |||||||
chr11:46665794 | T | TTCC | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136+277_1136+279d others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665794 | ||||||
chr11:46665797 | C | CT | 29 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0096 others(26): Show |
30 | HG01109.hp1 HG01192.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1136+302dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | ||||||
chr11:46665797 | C | CTT | 5 | a0001c0001t0002g0065 a0001c0001t0004g0039 a0001c0001t0004g0042 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+301_1136+302d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | ||||||
chr11:46665797 | C | CTTTTT | 24 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(21): Show |
25 | HG01070.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1136+298_1136+302d others(7): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | ||||||
chr11:46665797 | C | CTTTTTT | 11 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0022 others(8): Show |
11 | HG00735.hp1 HG01361.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1136+297_1136+302d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | ||||||
chr11:46666074 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1136+555G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666074 | |||||||
chr11:46666137 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1136+618A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666137 | |||||||
chr11:46666159 | C | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0160 a0001c0001t0001g0162 |
3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1136+640C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666159 | |||||||
chr11:46666321 | C | G | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+802C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666321 | |||||||
chr11:46666582 | A | C | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1136+1063A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666582 | |||||||
chr11:46666659 | G | A | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-1114G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666659 | |||||||
chr11:46666819 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0094 |
2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1137-954C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666819 | |||||||
chr11:46666862 | AT | A | 6 | a0001c0001t0002g0053 a0001c0002t0005g0204 a0001c0002t0005g0207 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-900delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46666862 | ||||||
chr11:46666875 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1137-898A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666875 | |||||||
chr11:46666989 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137-784C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666989 | |||||||
chr11:46667010 | G | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1137-763G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667010 | |||||||
chr11:46667122 | G | A | 1 | a0001c0001t0014g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1137-651G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667122 | |||||||
chr11:46667632 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0010g0089 |
2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1137-141A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667632 | |||||||
chr11:46667674 | T | C | 1 | a0001c0001t0008g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1137-99T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667674 | |||||||
chr11:46667724 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1137-49G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667724 | |||||||
chr11:46668015 | G | T | 1 | a0001c0001t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1251+128G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668015 | |||||||
chr11:46668106 | C | T | 23 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(20): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1251+219C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668106 | |||||||
chr11:46668181 | T | C | 1 | a0001c0001t0008g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1251+294T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668181 | |||||||
chr11:46668223 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0070 others(6): Show |
10 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1252-276A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668223 | |||||||
chr11:46668439 | A | G | 2 | a0001c0003t0005g0205 a0001c0003t0005g0206 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1252-60A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668439 | |||||||
chr11:46668588 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1329+12G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 16/18 | chr11 | 46668588 | |||||||
chr11:46668704 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(4): Show |
8 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1330-90A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 16/18 | chr11 | 46668704 | |||||||
chr11:46669165 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0070 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1447-239G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669165 | |||||||
chr11:46669217 | C | T | 1 | a0001c0001t0019g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1447-187C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669217 | |||||||
chr11:46669273 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-131G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669273 | |||||||
chr11:46669542 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1575+10C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46669542 | |||||||
chr11:46669767 | C | A | 5 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+235C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46669767 | |||||||
chr11:46670046 | G | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+514G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670046 | |||||||
chr11:46670055 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1575+523A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670055 | |||||||
chr11:46670187 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(83): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1575+655A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670187 | |||||||
chr11:46670495 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+963A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670495 | |||||||
chr11:46670497 | AG | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
23 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1575+966delG | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670497 | |||||||
chr11:46670862 | A | G | 1 | a0001c0001t0003g0076 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1575+1330A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670862 | |||||||
chr11:46670887 | C | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0091 others(3): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+1355C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670887 | |||||||
chr11:46671139 | C | T | 24 | a0001c0001t0003g0076 a0001c0001t0003g0082 a0001c0001t0003g0102 others(21): Show |
24 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-1116C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671139 | |||||||
chr11:46671202 | TC | T | 2 | a0001c0002t0020g0030 a0001c0002t0021g0031 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1576-1052delC | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671202 | |||||||
chr11:46671320 | C | T | 61 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(58): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1576-935C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671320 | |||||||
chr11:46671409 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0195 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1576-846A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671409 | |||||||
chr11:46671514 | G | T | 11 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1576-741G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671514 | |||||||
chr11:46671610 | G | A | 7 | a0001c0002t0005g0204 a0001c0002t0005g0207 a0001c0002t0005g0208 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-645G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671610 | |||||||
chr11:46671619 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(36): Show |
40 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1576-636G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671619 | |||||||
chr11:46671752 | T | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0019 |
2 | NA18942.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1576-503T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671752 |