Item | Value |
---|---|
geneid | 178 |
ensemblid | ENSG00000162688.17 |
hgncid | 321 |
symbol | AGL |
name | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase |
refseq_nuc | NM_000642.3 |
refseq_prot | NP_000633.2 |
ensembl_nuc | ENST00000361915.8 |
ensembl_prot | ENSP00000355106.3 |
mane_status | MANE Select |
chr | chr1 |
start | 99850361 |
end | 99924020 |
strand | + |
ver | v1.2 |
region | chr1:99850361-99924020 |
region5000 | chr1:99845361-99929020 |
regionname0 | AGL_chr1_99850361_99924020 |
regionname5000 | AGL_chr1_99845361_99929020 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1532 | 183 | 43 | 39 | 71 | 3 | 25 | 53 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0002 | 0/0 | 1532 | 35 | 0 | 7 | 26 | 0 | 2 | 23 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0003 | 0/0 | 1532 | 23 | 11 | 6 | 6 | 0 | 0 | 3 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0004 | 0/0 | 1532 | 22 | 3 | 4 | 8 | 2 | 5 | 8 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0005 | 0/0 | 1532 | 22 | 0 | 2 | 15 | 0 | 5 | 11 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0006 | 0/0 | 1532 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0007 | 0/0 | 1532 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0008 | 0/0 | 1532 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0009 | 0/0 | 1532 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0010 | 0/0 | 1532 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0011 | 0/0 | 1532 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0012 | 0/0 | 1532 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0013 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0014 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0015 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0016 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0017 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0018 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0019 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0020 | 0/0 | 1532 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0021 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0022 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0023 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0024 | 0/0 | 1532 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
a0025 | 0/0 | 1532 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | MGHSK others(1527): Show |
chr1 | 99845361 | 99929020 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4596 | 125 | 38 | 21 | 47 | 2 | 17 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0001c0002 | 1/1 | 4596 | 53 | 2 | 18 | 22 | 1 | 8 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0001c0014 | 0/0 | 4596 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0001c0020 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0001c0022 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0001c0031 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0002c0003 | 0/0 | 4596 | 25 | 0 | 7 | 17 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0002c0007 | 0/0 | 4596 | 10 | 0 | 0 | 9 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0003c0006 | 0/0 | 4596 | 21 | 9 | 6 | 6 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0003c0015 | 0/0 | 4596 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0004c0004 | 0/0 | 4596 | 22 | 3 | 4 | 8 | 2 | 5 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0005c0005 | 0/0 | 4596 | 21 | 0 | 2 | 14 | 0 | 5 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0005c0018 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0006c0008 | 0/0 | 4596 | 5 | 5 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0007c0009 | 0/0 | 4596 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0007c0024 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0008c0013 | 0/0 | 4596 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0008c0032 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0009c0010 | 0/0 | 4596 | 3 | 3 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0010c0011 | 0/0 | 4596 | 2 | 0 | 1 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0011c0012 | 0/0 | 4596 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0012c0033 | 0/0 | 4596 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0013c0028 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0014c0019 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0015c0021 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0016c0025 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0017c0030 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0018c0027 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0019c0029 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0020c0034 | 0/0 | 4596 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0021c0035 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0022c0023 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0023c0026 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0024c0016 | 0/0 | 4596 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 | ||
a0025c0017 | 0/0 | 4596 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ATGGG others(4591): Show |
chr1 | 99845361 | 99929020 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7091 | 36 | 20 | 1 | 13 | 1 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0002 | 0/0 | 7091 | 46 | 3 | 13 | 24 | 1 | 5 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0003 | 0/0 | 7091 | 27 | 2 | 4 | 10 | 0 | 11 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0005 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0006 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0007 | 0/0 | 7091 | 6 | 6 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0008 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0009 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0011 | 0/0 | 7091 | 3 | 3 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0001t0017 | 0/0 | 7091 | 2 | 0 | 2 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0001 | 1/1 | 7091 | 46 | 0 | 17 | 18 | 1 | 8 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0005 | 0/0 | 7091 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0006 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0008 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0018 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0020 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0002t0022 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0014t0016 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0020t0001 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0022t0001 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0001c0031t0006 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0003t0005 | 0/0 | 7091 | 16 | 0 | 4 | 12 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0003t0006 | 0/0 | 7091 | 8 | 0 | 2 | 5 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0003t0021 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0007t0002 | 0/0 | 7091 | 6 | 0 | 0 | 6 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0007t0005 | 0/0 | 7091 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0002c0007t0006 | 0/0 | 7091 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0003c0006t0001 | 0/0 | 7091 | 17 | 6 | 5 | 6 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0003c0006t0006 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0003c0006t0008 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0003c0006t0019 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0003c0015t0012 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0004c0004t0003 | 0/0 | 7091 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0004c0004t0004 | 0/0 | 7091 | 20 | 3 | 3 | 8 | 2 | 4 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0004c0004t0015 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0005c0005t0002 | 0/0 | 7091 | 18 | 0 | 1 | 13 | 0 | 4 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0005c0005t0003 | 0/0 | 7091 | 3 | 0 | 1 | 1 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0005c0018t0005 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0006c0008t0007 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0006c0008t0008 | 0/0 | 7091 | 3 | 3 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0007c0009t0004 | 0/0 | 7091 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0007c0024t0015 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0008c0013t0004 | 0/0 | 7091 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0008c0032t0004 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0009c0010t0010 | 0/0 | 7091 | 3 | 3 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0010c0011t0014 | 0/0 | 7088 | 2 | 0 | 1 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7083): Show |
chr1 | 99845361 | 99929020 |
a0011c0012t0006 | 0/0 | 7091 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0012c0033t0004 | 0/0 | 7091 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0013c0028t0002 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0014c0019t0001 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0015c0021t0001 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0016c0025t0001 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0017c0030t0006 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0018c0027t0013 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0019c0029t0013 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0020c0034t0005 | 0/0 | 7091 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0021c0035t0001 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0022c0023t0004 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0023c0026t0009 | 0/0 | 7091 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
a0024c0016t0023 | 0/0 | 7088 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7083): Show |
chr1 | 99845361 | 99929020 |
a0025c0017t0001 | 0/0 | 7091 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | ACCAG others(7086): Show |
chr1 | 99845361 | 99929020 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0017g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0001t0017g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0020g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0002t0022g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0014t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0014t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0020t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0022t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0001c0031t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0003t0021g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0002c0007t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0006t0019g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0015t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0003c0015t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0004c0004t0015g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0005t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0005c0018t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0006c0008t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0006c0008t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0006c0008t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0006c0008t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0007c0009t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0007c0009t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0007c0009t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0007c0024t0015g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0008c0013t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0008c0013t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0008c0032t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0009c0010t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0009c0010t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0009c0010t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0010c0011t0014g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0010c0011t0014g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0011c0012t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0012c0033t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0013c0028t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0014c0019t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0015c0021t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0016c0025t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0017c0030t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0018c0027t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0019c0029t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0020c0034t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0021c0035t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0022c0023t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0023c0026t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0024c0016t0023g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
a0025c0017t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0004 | c0004 | t0004 | g0248 | EUR | GBR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00423 | hp1 | a0005 | c0005 | t0002 | g0121 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00597 | hp2 | a0007 | c0009 | t0004 | g0071 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00639 | hp2 | a0002 | c0003 | t0005 | g0051 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00642 | hp2 | a0003 | c0006 | t0019 | g0186 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00673 | hp1 | a0003 | c0006 | t0001 | g0180 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00733 | hp1 | a0005 | c0005 | t0003 | g0130 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00733 | hp2 | a0002 | c0003 | t0006 | g0065 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG00741 | hp2 | a0004 | c0004 | t0004 | g0267 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01069 | hp2 | a0002 | c0003 | t0021 | g0061 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01074 | hp2 | a0001 | c0002 | t0020 | g0021 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01167 | hp2 | a0010 | c0011 | t0014 | g0202 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0250 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01257 | hp1 | a0001 | c0001 | t0017 | g0137 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01258 | hp2 | a0001 | c0001 | t0017 | g0136 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01261 | hp2 | a0002 | c0003 | t0005 | g0022 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01358 | hp2 | a0002 | c0003 | t0005 | g0055 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01361 | hp1 | a0002 | c0003 | t0006 | g0066 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01361 | hp2 | a0012 | c0033 | t0004 | g0016 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01496 | hp2 | a0004 | c0004 | t0015 | g0132 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01517 | hp1 | a0004 | c0004 | t0004 | g0251 | EUR | IBS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | IBS | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01928 | hp2 | a0003 | c0006 | t0001 | g0175 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01934 | hp1 | a0003 | c0006 | t0001 | g0189 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01981 | hp1 | a0004 | c0004 | t0004 | g0259 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01981 | hp2 | a0003 | c0006 | t0001 | g0198 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01993 | hp1 | a0005 | c0005 | t0002 | g0124 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01993 | hp2 | a0002 | c0003 | t0005 | g0092 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02004 | hp1 | a0004 | c0004 | t0004 | g0016 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02027 | hp1 | a0013 | c0028 | t0002 | g0247 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02055 | hp1 | a0003 | c0015 | t0012 | g0197 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02071 | hp1 | a0007 | c0009 | t0004 | g0090 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02071 | hp2 | a0003 | c0006 | t0001 | g0199 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02080 | hp2 | a0003 | c0006 | t0001 | g0179 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02129 | hp1 | a0002 | c0007 | t0005 | g0277 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02129 | hp2 | a0014 | c0019 | t0001 | g0038 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02132 | hp2 | a0015 | c0021 | t0001 | g0020 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02135 | hp1 | a0002 | c0007 | t0005 | g0285 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02148 | hp1 | a0003 | c0006 | t0001 | g0184 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02155 | hp2 | a0005 | c0005 | t0002 | g0112 | EAS | CDX | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | CDX | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02257 | hp1 | a0001 | c0002 | t0008 | g0087 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02257 | hp2 | a0003 | c0006 | t0001 | g0183 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02258 | hp1 | a0016 | c0025 | t0001 | g0294 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0106 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02280 | hp1 | a0003 | c0006 | t0001 | g0194 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02280 | hp2 | a0003 | c0006 | t0001 | g0190 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02293 | hp2 | a0003 | c0006 | t0001 | g0181 | AMR | PEL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02451 | hp1 | a0003 | c0015 | t0012 | g0195 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02451 | hp2 | a0006 | c0008 | t0007 | g0228 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02523 | hp1 | a0005 | c0005 | t0002 | g0115 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02523 | hp2 | a0005 | c0005 | t0002 | g0116 | EAS | KHV | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02602 | hp1 | a0002 | c0007 | t0006 | g0266 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02602 | hp2 | a0005 | c0005 | t0002 | g0127 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02622 | hp1 | a0003 | c0006 | t0006 | g0191 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02630 | hp2 | a0008 | c0013 | t0004 | g0019 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02647 | hp1 | a0008 | c0013 | t0004 | g0063 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02647 | hp2 | a0017 | c0030 | t0006 | g0272 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02683 | hp1 | a0002 | c0003 | t0006 | g0064 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02717 | hp1 | a0009 | c0010 | t0010 | g0205 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02738 | hp2 | a0005 | c0005 | t0002 | g0166 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02809 | hp1 | a0001 | c0002 | t0018 | g0044 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02809 | hp2 | a0003 | c0006 | t0001 | g0193 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02886 | hp2 | a0009 | c0010 | t0010 | g0206 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02976 | hp1 | a0006 | c0008 | t0007 | g0239 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03017 | hp1 | a0004 | c0004 | t0004 | g0260 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03098 | hp1 | a0001 | c0031 | t0006 | g0244 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03098 | hp2 | a0018 | c0027 | t0013 | g0200 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03130 | hp1 | a0001 | c0014 | t0016 | g0165 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03130 | hp2 | a0003 | c0006 | t0006 | g0192 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03139 | hp2 | a0019 | c0029 | t0013 | g0212 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03209 | hp2 | a0006 | c0008 | t0008 | g0018 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0231 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03486 | hp1 | a0003 | c0006 | t0001 | g0182 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03490 | hp1 | a0004 | c0004 | t0004 | g0261 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03516 | hp2 | a0001 | c0014 | t0016 | g0133 | AFR | ESN | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0229 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03579 | hp1 | a0004 | c0004 | t0004 | g0249 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03669 | hp2 | a0004 | c0004 | t0004 | g0253 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03688 | hp1 | a0004 | c0004 | t0004 | g0262 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03927 | hp1 | a0005 | c0005 | t0003 | g0118 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03927 | hp2 | a0010 | c0011 | t0014 | g0245 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03942 | hp1 | a0005 | c0005 | t0002 | g0125 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04115 | hp1 | a0004 | c0004 | t0003 | g0240 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04184 | hp2 | a0020 | c0034 | t0005 | g0196 | SAS | BEB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04228 | hp1 | a0005 | c0005 | t0002 | g0122 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | STU | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18522 | hp1 | a0009 | c0010 | t0010 | g0207 | AFR | YRI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18612 | hp1 | a0007 | c0024 | t0015 | g0234 | EAS | CHB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18612 | hp2 | a0002 | c0003 | t0005 | g0104 | EAS | CHB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18939 | hp2 | a0004 | c0004 | t0004 | g0252 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18942 | hp2 | a0002 | c0003 | t0005 | g0053 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18944 | hp1 | a0002 | c0003 | t0005 | g0089 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18945 | hp2 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18947 | hp1 | a0001 | c0002 | t0005 | g0083 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18948 | hp1 | a0005 | c0018 | t0005 | g0049 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18948 | hp2 | a0003 | c0006 | t0001 | g0178 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18951 | hp1 | a0004 | c0004 | t0004 | g0254 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18952 | hp1 | a0005 | c0005 | t0002 | g0149 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18952 | hp2 | a0002 | c0003 | t0005 | g0052 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18953 | hp1 | a0002 | c0003 | t0006 | g0097 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18953 | hp2 | a0001 | c0002 | t0005 | g0058 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18960 | hp2 | a0007 | c0009 | t0004 | g0054 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18962 | hp2 | a0021 | c0035 | t0001 | g0185 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18963 | hp1 | a0005 | c0005 | t0002 | g0162 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18964 | hp2 | a0002 | c0003 | t0005 | g0088 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18967 | hp1 | a0005 | c0005 | t0002 | g0171 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18967 | hp2 | a0011 | c0012 | t0006 | g0007 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18968 | hp1 | a0001 | c0002 | t0006 | g0042 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18970 | hp1 | a0003 | c0006 | t0001 | g0177 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18970 | hp2 | a0005 | c0005 | t0002 | g0110 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18971 | hp1 | a0005 | c0005 | t0003 | g0128 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18971 | hp2 | a0004 | c0004 | t0004 | g0256 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18972 | hp1 | a0004 | c0004 | t0004 | g0265 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18972 | hp2 | a0002 | c0007 | t0005 | g0288 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18973 | hp1 | a0001 | c0020 | t0001 | g0023 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18981 | hp1 | a0002 | c0007 | t0002 | g0155 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18983 | hp2 | a0005 | c0005 | t0002 | g0126 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18989 | hp2 | a0005 | c0005 | t0002 | g0109 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18994 | hp1 | a0005 | c0005 | t0002 | g0123 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18994 | hp2 | a0011 | c0012 | t0006 | g0007 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18999 | hp2 | a0002 | c0003 | t0006 | g0068 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19002 | hp1 | a0001 | c0022 | t0001 | g0095 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19002 | hp2 | a0001 | c0002 | t0022 | g0093 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19003 | hp1 | a0002 | c0003 | t0006 | g0094 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19003 | hp2 | a0002 | c0007 | t0002 | g0154 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19007 | hp2 | a0005 | c0005 | t0002 | g0131 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19010 | hp1 | a0004 | c0004 | t0004 | g0263 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19010 | hp2 | a0002 | c0007 | t0002 | g0003 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19012 | hp2 | a0004 | c0004 | t0004 | g0264 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0174 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19043 | hp1 | a0022 | c0023 | t0004 | g0017 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19056 | hp1 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19056 | hp2 | a0002 | c0003 | t0005 | g0026 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19057 | hp2 | a0002 | c0003 | t0006 | g0067 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19058 | hp2 | a0002 | c0003 | t0005 | g0057 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19062 | hp1 | a0002 | c0007 | t0002 | g0003 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19062 | hp2 | a0002 | c0003 | t0006 | g0096 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19064 | hp1 | a0005 | c0005 | t0002 | g0169 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19066 | hp2 | a0002 | c0003 | t0005 | g0056 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19068 | hp2 | a0003 | c0006 | t0001 | g0176 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19070 | hp1 | a0002 | c0007 | t0002 | g0003 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19072 | hp1 | a0002 | c0003 | t0005 | g0048 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19076 | hp2 | a0002 | c0003 | t0005 | g0050 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19081 | hp2 | a0002 | c0003 | t0005 | g0045 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19088 | hp1 | a0002 | c0003 | t0005 | g0105 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19091 | hp1 | a0002 | c0007 | t0002 | g0156 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19240 | hp1 | a0004 | c0004 | t0004 | g0017 | AFR | YRI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA19240 | hp2 | a0023 | c0026 | t0009 | g0209 | AFR | YRI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20752 | hp1 | a0024 | c0016 | t0023 | g0203 | EUR | TSI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0027 | EUR | TSI | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | GIH | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20905 | hp2 | a0025 | c0017 | t0001 | g0059 | SAS | GIH | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02109 | hp2 | a0006 | c0008 | t0008 | g0201 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0226 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02486 | hp2 | a0003 | c0006 | t0008 | g0188 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02559 | hp1 | a0004 | c0004 | t0004 | g0255 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | ACB | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03471 | hp1 | a0003 | c0006 | t0001 | g0187 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0238 | AFR | MSL | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG06807 | hp1 | a0006 | c0008 | t0008 | g0018 | AFR | USA | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
HG06807 | hp2 | a0008 | c0032 | t0004 | g0214 | AFR | USA | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | USA | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | USA | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | LWK | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0070 | REF | REF | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0047 | REF | REF | AGL_chr1_99845361_99929020 | AGL | chr1 | 99845361 | 99929020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99861532 | A | G | 1 | a0009 | 3 | HG02717.hp1 HG02886.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.112A>G | p.Thr38Ala | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/34 | 235/7091 | 112/4599 | 38/1532 | chr1 | 99861532 | |||
chr1:99862406 | G | A | 1 | a0025 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.443G>A | p.Arg148Lys | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/34 | 566/7091 | 443/4599 | 148/1532 | chr1 | 99862406 | |||
chr1:99870421 | A | G | 3 | a0003 a0020 a0021 |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
missense_variant | MODERATE | c.686A>G | p.Gln229Arg | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 6/34 | 809/7091 | 686/4599 | 229/1532 | chr1 | 99870421 | |||
chr1:99875190 | G | T | 1 | a0012 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1119G>T | p.Trp373Cys | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 9/34 | 1242/7091 | 1119/4599 | 373/1532 | chr1 | 99875190 | |||
chr1:99875226 | G | T | 2 | a0010 a0024 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.1155G>T | p.Lys385Asn | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 9/34 | 1278/7091 | 1155/4599 | 385/1532 | chr1 | 99875226 | |||
chr1:99875231 | G | A | 2 | a0005 a0020 |
23 | HG00423.hp1 HG00733.hp1 HG01993.hp1 others(20): Show |
missense_variant | MODERATE | c.1160G>A | p.Arg387Gln | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 9/34 | 1283/7091 | 1160/4599 | 387/1532 | chr1 | 99875231 | |||
chr1:99876493 | C | T | 1 | a0008 | 3 | HG02630.hp2 HG02647.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1319C>T | p.Ser440Phe | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/34 | 1442/7091 | 1319/4599 | 440/1532 | chr1 | 99876493 | |||
chr1:99880005 | A | G | 1 | a0012 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1694A>G | p.Asn565Ser | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 13/34 | 1817/7091 | 1694/4599 | 565/1532 | chr1 | 99880005 | |||
chr1:99880706 | T | G | 1 | a0022 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1810T>G | p.Phe604Val | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 14/34 | 1933/7091 | 1810/4599 | 604/1532 | chr1 | 99880706 | |||
chr1:99881391 | G | T | 1 | a0011 | 2 | NA18967.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.2101G>T | p.Ala701Ser | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 16/34 | 2224/7091 | 2101/4599 | 701/1532 | chr1 | 99881391 | |||
chr1:99884427 | C | T | 1 | a0010 | 2 | HG01167.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.2522C>T | p.Ser841Phe | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 19/34 | 2645/7091 | 2522/4599 | 841/1532 | chr1 | 99884427 | |||
chr1:99884692 | T | G | 1 | a0021 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2670T>G | p.Ile890Met | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/34 | 2793/7091 | 2670/4599 | 890/1532 | chr1 | 99884692 | |||
chr1:99891292 | C | G | 2 | a0009 a0017 |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.2885C>G | p.Ser962Cys | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 22/34 | 3008/7091 | 2885/4599 | 962/1532 | chr1 | 99891292 | |||
chr1:99892547 | C | T | 3 | a0004 a0012 a0022 |
24 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(21): Show |
missense_variant | MODERATE | c.3199C>T | p.Pro1067Ser | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/34 | 3322/7091 | 3199/4599 | 1067/1532 | chr1 | 99892547 | |||
chr1:99896369 | G | A | 4 | a0002 a0007 a0008 others(1): Show |
44 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
missense_variant | MODERATE | c.3343G>A | p.Gly1115Arg | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/34 | 3466/7091 | 3343/4599 | 1115/1532 | chr1 | 99896369 | |||
chr1:99900692 | T | G | 1 | a0016 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3419T>G | p.Leu1140Arg | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/34 | 3542/7091 | 3419/4599 | 1140/1532 | chr1 | 99900692 | |||
chr1:99902713 | G | A | 1 | a0006 | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.3619G>A | p.Ala1207Thr | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/34 | 3742/7091 | 3619/4599 | 1207/1532 | chr1 | 99902713 | |||
chr1:99910769 | G | A | 2 | a0007 a0008 |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
missense_variant | MODERATE | c.3758G>A | p.Arg1253His | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/34 | 3881/7091 | 3758/4599 | 1253/1532 | chr1 | 99910769 | |||
chr1:99910775 | A | G | 1 | a0019 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.3764A>G | p.Asn1255Ser | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/34 | 3887/7091 | 3764/4599 | 1255/1532 | chr1 | 99910775 | |||
chr1:99913604 | G | A | 1 | a0014 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.4027G>A | p.Glu1343Lys | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/34 | 4150/7091 | 4027/4599 | 1343/1532 | chr1 | 99913604 | |||
chr1:99913652 | C | T | 1 | a0015 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.4075C>T | p.Arg1359Cys | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/34 | 4198/7091 | 4075/4599 | 1359/1532 | chr1 | 99913652 | |||
chr1:99916662 | C | T | 1 | a0013 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.4412C>T | p.Pro1471Leu | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/34 | 4535/7091 | 4412/4599 | 1471/1532 | chr1 | 99916662 | |||
chr1:99916680 | C | G | 2 | a0018 a0019 |
2 | HG03098.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.4430C>G | p.Thr1477Ser | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/34 | 4553/7091 | 4430/4599 | 1477/1532 | chr1 | 99916680 | |||
chr1:99916700 | G | A | 1 | a0023 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.4450G>A | p.Val1484Ile | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/34 | 4573/7091 | 4450/4599 | 1484/1532 | chr1 | 99916700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99861627 | T | C | 2 | a0010c0011 a0024c0016 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.207T>C | p.Asn69Asn | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/34 | 330/7091 | 207/4599 | 69/1532 | chr1 | 99861627 | |||
chr1:99870805 | C | T | 24 | a0001c0001 a0001c0014 a0001c0031 others(21): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
synonymous_variant | LOW | c.894C>T | p.Leu298Leu | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/34 | 1017/7091 | 894/4599 | 298/1532 | chr1 | 99870805 | |||
chr1:99888098 | A | C | 1 | a0001c0014 | 2 | HG03130.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.2802A>C | p.Ala934Ala | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/34 | 2925/7091 | 2802/4599 | 934/1532 | chr1 | 99888098 | |||
chr1:99891290 | A | G | 1 | a0001c0031 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2883A>G | p.Arg961Arg | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 22/34 | 3006/7091 | 2883/4599 | 961/1532 | chr1 | 99891290 | |||
chr1:99900657 | G | A | 1 | a0001c0031 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.3384G>A | p.Ala1128Ala | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/34 | 3507/7091 | 3384/4599 | 1128/1532 | chr1 | 99900657 | |||
chr1:99900816 | A | G | 1 | a0001c0022 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.3543A>G | p.Arg1181Arg | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/34 | 3666/7091 | 3543/4599 | 1181/1532 | chr1 | 99900816 | |||
chr1:99910803 | A | T | 1 | a0003c0015 | 2 | HG02055.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.3792A>T | p.Gly1264Gly | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/34 | 3915/7091 | 3792/4599 | 1264/1532 | chr1 | 99910803 | |||
chr1:99912417 | T | C | 2 | a0010c0011 a0024c0016 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.3849T>C | p.Ala1283Ala | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/34 | 3972/7091 | 3849/4599 | 1283/1532 | chr1 | 99912417 | |||
chr1:99916413 | T | C | 1 | a0001c0020 | 1 | NA18973.hp1 | synonymous_variant | LOW | c.4263T>C | p.Asp1421Asp | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 32/34 | 4386/7091 | 4263/4599 | 1421/1532 | chr1 | 99916413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99851033 | A | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(12): Show |
122 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/34 | chr1 | 99851033 | |||||||
chr1:99921832 | A | G | 1 | a0024c0016t0023 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 181 | chr1 | 99921832 | ||||||
chr1:99921923 | G | T | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0017 others(8): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*272G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 272 | chr1 | 99921923 | ||||||
chr1:99922046 | C | T | 1 | a0001c0002t0022 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 395 | chr1 | 99922046 | ||||||
chr1:99922226 | G | T | 3 | a0001c0001t0009 a0001c0001t0011 a0023c0026t0009 |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*575G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 575 | chr1 | 99922226 | ||||||
chr1:99922383 | C | T | 44 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(41): Show |
177 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*732C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 732 | chr1 | 99922383 | ||||||
chr1:99922390 | A | G | 2 | a0010c0011t0014 a0024c0016t0023 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*739A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 739 | chr1 | 99922390 | ||||||
chr1:99922610 | CATG | C | 2 | a0010c0011t0014 a0024c0016t0023 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*962_*964delGAT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 962 | INFO_REALIGN_3_PRIME | chr1 | 99922610 | |||||
chr1:99922679 | C | T | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(32): Show |
145 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1028C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1028 | chr1 | 99922679 | ||||||
chr1:99922895 | T | A | 3 | a0001c0001t0009 a0001c0001t0011 a0023c0026t0009 |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1244T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1244 | chr1 | 99922895 | ||||||
chr1:99922929 | A | G | 1 | a0003c0015t0012 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1278A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1278 | chr1 | 99922929 | ||||||
chr1:99922929 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1278 | chr1 | 99922929 | ||||||
chr1:99922932 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1281 | chr1 | 99922932 | ||||||
chr1:99922934 | G | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1283G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1283 | chr1 | 99922934 | ||||||
chr1:99922935 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1284 | chr1 | 99922935 | ||||||
chr1:99922937 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1286 | chr1 | 99922937 | ||||||
chr1:99922939 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1288A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1288 | chr1 | 99922939 | ||||||
chr1:99922940 | G | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1289 | chr1 | 99922940 | ||||||
chr1:99922942 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1291 | chr1 | 99922942 | ||||||
chr1:99922944 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1293T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1293 | chr1 | 99922944 | ||||||
chr1:99922945 | T | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1294T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1294 | chr1 | 99922945 | ||||||
chr1:99922947 | A | C | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(14): Show |
111 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1296A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1296 | chr1 | 99922947 | ||||||
chr1:99922950 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1299A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1299 | chr1 | 99922950 | ||||||
chr1:99922953 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1302A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1302 | chr1 | 99922953 | ||||||
chr1:99922957 | C | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1306C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1306 | chr1 | 99922957 | ||||||
chr1:99922958 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1307C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1307 | chr1 | 99922958 | ||||||
chr1:99922961 | C | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1310 | chr1 | 99922961 | ||||||
chr1:99922962 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1311A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1311 | chr1 | 99922962 | ||||||
chr1:99922964 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1313A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1313 | chr1 | 99922964 | ||||||
chr1:99922965 | C | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1314 | chr1 | 99922965 | ||||||
chr1:99922968 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1317A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1317 | chr1 | 99922968 | ||||||
chr1:99922971 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1320C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1320 | chr1 | 99922971 | ||||||
chr1:99922972 | T | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1321T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1321 | chr1 | 99922972 | ||||||
chr1:99922973 | T | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1322 | chr1 | 99922973 | ||||||
chr1:99922977 | G | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1326 | chr1 | 99922977 | ||||||
chr1:99922980 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1329 | chr1 | 99922980 | ||||||
chr1:99922983 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1332A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1332 | chr1 | 99922983 | ||||||
chr1:99922984 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1333A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1333 | chr1 | 99922984 | ||||||
chr1:99922985 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1334 | chr1 | 99922985 | ||||||
chr1:99922987 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1336A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1336 | chr1 | 99922987 | ||||||
chr1:99922989 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1338 | chr1 | 99922989 | ||||||
chr1:99922995 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1344 | chr1 | 99922995 | ||||||
chr1:99922997 | G | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1346 | chr1 | 99922997 | ||||||
chr1:99922998 | C | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1347 | chr1 | 99922998 | ||||||
chr1:99922999 | T | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1348T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1348 | chr1 | 99922999 | ||||||
chr1:99923005 | T | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1354 | chr1 | 99923005 | ||||||
chr1:99923006 | G | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1355G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1355 | chr1 | 99923006 | ||||||
chr1:99923007 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1356 | chr1 | 99923007 | ||||||
chr1:99923011 | A | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1360A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1360 | chr1 | 99923011 | ||||||
chr1:99923012 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1361 | chr1 | 99923012 | ||||||
chr1:99923015 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1364C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1364 | chr1 | 99923015 | ||||||
chr1:99923016 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1365 | chr1 | 99923016 | ||||||
chr1:99923018 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1367 | chr1 | 99923018 | ||||||
chr1:99923020 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1369 | chr1 | 99923020 | ||||||
chr1:99923021 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1370 | chr1 | 99923021 | ||||||
chr1:99923022 | T | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1371 | chr1 | 99923022 | ||||||
chr1:99923030 | C | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1379C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1379 | chr1 | 99923030 | ||||||
chr1:99923032 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1381T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1381 | chr1 | 99923032 | ||||||
chr1:99923034 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1383T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1383 | chr1 | 99923034 | ||||||
chr1:99923035 | A | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1384 | chr1 | 99923035 | ||||||
chr1:99923037 | T | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1386 | chr1 | 99923037 | ||||||
chr1:99923038 | T | A | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1387T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1387 | chr1 | 99923038 | ||||||
chr1:99923048 | A | T | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1397 | chr1 | 99923048 | ||||||
chr1:99923049 | T | C | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1398 | chr1 | 99923049 | ||||||
chr1:99923050 | T | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1399T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1399 | chr1 | 99923050 | ||||||
chr1:99923052 | T | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1401 | chr1 | 99923052 | ||||||
chr1:99923056 | C | G | 1 | a0001c0002t0020 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1405 | chr1 | 99923056 | ||||||
chr1:99923192 | T | C | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(20): Show |
121 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1541T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1541 | chr1 | 99923192 | ||||||
chr1:99923204 | T | G | 1 | a0003c0015t0012 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1553T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1553 | chr1 | 99923204 | ||||||
chr1:99923209 | T | C | 1 | a0002c0003t0021 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1558T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1558 | chr1 | 99923209 | ||||||
chr1:99923261 | T | C | 1 | a0002c0003t0021 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1610 | chr1 | 99923261 | ||||||
chr1:99923567 | T | C | 1 | a0001c0002t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 1916 | chr1 | 99923567 | ||||||
chr1:99923709 | G | A | 1 | a0003c0006t0019 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 2058 | chr1 | 99923709 | ||||||
chr1:99923834 | T | G | 1 | a0001c0001t0017 | 2 | HG01257.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2183T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 34/34 | 2183 | chr1 | 99923834 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99850448 | G | A | 1 | a0008c0013t0004g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-69+33G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 1/33 | chr1 | 99850448 | |||||||
chr1:99850806 | G | GAAACAAC others(68): Show |
1 | a0015c0021t0001g0020 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-68-163_-68-89dupA others(74): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 99850806 | ||||||
chr1:99851209 | C | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.82+85C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851209 | |||||||
chr1:99851391 | A | C | 1 | a0001c0001t0002g0295 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.82+267A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851391 | |||||||
chr1:99851400 | T | C | 2 | a0001c0001t0009g0106 a0001c0001t0009g0107 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.82+276T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851400 | |||||||
chr1:99851553 | G | T | 1 | a0002c0003t0005g0105 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.82+429G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851553 | |||||||
chr1:99851838 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.82+714A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851838 | |||||||
chr1:99851915 | T | TA | 75 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(72): Show |
85 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.82+792dupA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99851915 | ||||||
chr1:99851952 | T | C | 25 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.82+828T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99851952 | |||||||
chr1:99852080 | A | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.82+956A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852080 | |||||||
chr1:99852214 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82+1090G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852214 | |||||||
chr1:99852351 | CT | C | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(168): Show |
189 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.82+1248delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99852351 | ||||||
chr1:99852351 | CTT | C | 28 | a0001c0001t0001g0257 a0001c0001t0002g0111 a0001c0001t0005g0250 others(25): Show |
29 | HG00140.hp1 HG00741.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.82+1247_82+1248del others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99852351 | ||||||
chr1:99852372 | T | C | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1248T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852372 | |||||||
chr1:99852417 | C | G | 2 | a0004c0004t0004g0017 a0022c0023t0004g0017 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.82+1293C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852417 | |||||||
chr1:99852478 | T | A | 2 | a0001c0001t0009g0106 a0001c0001t0009g0107 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.82+1354T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852478 | |||||||
chr1:99852536 | A | AT | 109 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0290 others(106): Show |
120 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.82+1432dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99852536 | ||||||
chr1:99852578 | G | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0101 others(1): Show |
4 | NA18973.hp1 NA19070.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+1454G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852578 | |||||||
chr1:99852689 | T | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+1565T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852689 | |||||||
chr1:99852818 | G | A | 1 | a0003c0006t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.82+1694G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852818 | |||||||
chr1:99852822 | C | G | 1 | a0001c0002t0001g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.82+1698C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99852822 | |||||||
chr1:99853043 | C | A | 1 | a0001c0001t0007g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.82+1919C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853043 | |||||||
chr1:99853332 | T | C | 25 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.82+2208T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853332 | |||||||
chr1:99853400 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82+2276T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853400 | |||||||
chr1:99853489 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.82+2365C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853489 | |||||||
chr1:99853502 | A | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+2378A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853502 | |||||||
chr1:99853545 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(12): Show |
16 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.82+2421C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853545 | |||||||
chr1:99853695 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2571C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853695 | |||||||
chr1:99853704 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2580A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853704 | |||||||
chr1:99853756 | G | A | 2 | a0002c0003t0005g0026 a0002c0003t0005g0105 |
2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.82+2632G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853756 | |||||||
chr1:99853912 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2788G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99853912 | |||||||
chr1:99854022 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.82+2898C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854022 | |||||||
chr1:99854108 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.82+2984C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854108 | |||||||
chr1:99854204 | T | A | 1 | a0018c0027t0013g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.82+3080T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854204 | |||||||
chr1:99854482 | G | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82+3358G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854482 | |||||||
chr1:99854517 | C | G | 1 | a0002c0007t0005g0288 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.82+3393C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854517 | |||||||
chr1:99854528 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.82+3404C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854528 | |||||||
chr1:99854538 | G | A | 2 | a0010c0011t0014g0202 a0010c0011t0014g0245 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.82+3414G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854538 | |||||||
chr1:99854696 | G | A | 1 | a0001c0002t0001g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.82+3572G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854696 | |||||||
chr1:99854704 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+3580C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854704 | |||||||
chr1:99854759 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82+3635G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854759 | |||||||
chr1:99854763 | CA | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(17): Show |
21 | HG01169.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.82+3654delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99854763 | ||||||
chr1:99854879 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0029 |
2 | HG01358.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.82+3755G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854879 | |||||||
chr1:99854889 | G | C | 1 | a0004c0004t0004g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82+3765G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854889 | |||||||
chr1:99854976 | G | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+3852G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99854976 | |||||||
chr1:99855106 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.82+3982C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855106 | |||||||
chr1:99855133 | G | A | 3 | a0003c0006t0001g0194 a0003c0015t0012g0195 a0003c0015t0012g0197 |
3 | HG02055.hp1 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.82+4009G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855133 | |||||||
chr1:99855150 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+4026A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855150 | |||||||
chr1:99855199 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.82+4075T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855199 | |||||||
chr1:99855257 | AG | A | 3 | a0004c0004t0004g0017 a0004c0004t0004g0249 a0022c0023t0004g0017 |
3 | HG03579.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.82+4135delG | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99855257 | ||||||
chr1:99855295 | G | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+4171G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855295 | |||||||
chr1:99855334 | CCCTCATA others(26): Show |
C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+4211_82+4243del others(33): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855334 | |||||||
chr1:99855473 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82+4349C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855473 | |||||||
chr1:99855541 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+4417C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855541 | |||||||
chr1:99855758 | A | G | 1 | a0001c0002t0001g0098 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82+4634A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855758 | |||||||
chr1:99855792 | C | T | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+4668C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855792 | |||||||
chr1:99855867 | T | C | 2 | a0002c0003t0005g0026 a0002c0003t0005g0105 |
2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.82+4743T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855867 | |||||||
chr1:99855913 | T | G | 3 | a0003c0006t0001g0176 a0003c0006t0001g0177 a0003c0006t0001g0178 |
3 | NA18948.hp2 NA18970.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.82+4789T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855913 | |||||||
chr1:99855925 | G | T | 1 | a0002c0003t0006g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.82+4801G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99855925 | |||||||
chr1:99856138 | A | G | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82+5014A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856138 | |||||||
chr1:99856222 | T | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+5098T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856222 | |||||||
chr1:99856238 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+5114A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856238 | |||||||
chr1:99856292 | ATCCCTTC others(17): Show |
A | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+5182_83-5174del others(24): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856292 | ||||||
chr1:99856298 | TCCTTCCT others(13): Show |
T | 125 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(122): Show |
137 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.83-5181_83-5162del others(20): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856298 | ||||||
chr1:99856302 | TCCTTCCT others(9): Show |
T | 8 | a0004c0004t0015g0132 a0005c0005t0002g0109 a0005c0005t0002g0123 others(5): Show |
8 | HG00733.hp1 HG01496.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+5186_83-5178del others(16): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856302 | ||||||
chr1:99856305 | TTCCTCCC | T | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82+5185_83-5188del others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856305 | ||||||
chr1:99856305 | TTCCTCCC others(16): Show |
T | 1 | a0020c0034t0005g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.82+5185_83-5172del others(23): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856305 | ||||||
chr1:99856305 | TTCCTCCC others(28): Show |
T | 1 | a0003c0006t0001g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82+5185_83-5160del others(35): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856305 | ||||||
chr1:99856306 | TCCTCCCT others(17): Show |
T | 2 | a0001c0001t0002g0143 a0001c0001t0009g0107 |
2 | HG02559.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.83-5181_83-5158del others(24): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856306 | ||||||
chr1:99856306 | TCCTCCCT others(21): Show |
T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0146 a0006c0008t0008g0201 |
3 | HG00642.hp1 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.83-5181_83-5154del others(28): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856306 | ||||||
chr1:99856306 | TCCTCCCT others(25): Show |
T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0268 others(48): Show |
57 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.83-5181_83-5150del others(32): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856306 | ||||||
chr1:99856306 | TCCTCCCT others(29): Show |
T | 24 | a0001c0001t0001g0257 a0001c0001t0005g0250 a0001c0001t0008g0258 others(21): Show |
25 | HG00140.hp1 HG01256.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-5181_83-5146del others(36): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856306 | ||||||
chr1:99856306 | TCCTCCCT others(37): Show |
T | 1 | a0004c0004t0004g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.83-5169_83-5126del others(44): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856306 | ||||||
chr1:99856307 | CCTCCCTC others(8): Show |
C | 17 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(14): Show |
17 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.82+5185_83-5180del others(15): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856307 | ||||||
chr1:99856310 | CCCTCCCT others(9): Show |
C | 4 | a0001c0001t0001g0213 a0002c0003t0005g0045 a0008c0032t0004g0214 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-5181_83-5166del others(16): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856310 | ||||||
chr1:99856314 | CCCTCCCT others(5): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83-5181_83-5170del others(12): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856314 | ||||||
chr1:99856322 | T | C | 7 | a0003c0006t0001g0193 a0003c0006t0001g0194 a0003c0006t0006g0191 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-5181T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856322 | |||||||
chr1:99856326 | T | C | 24 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(21): Show |
24 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.83-5177T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856326 | |||||||
chr1:99856326 | T | TCCTC | 17 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0025 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.83-5141_83-5138dup others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856326 | ||||||
chr1:99856354 | C | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0268 others(27): Show |
35 | HG00140.hp2 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.83-5149C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856354 | |||||||
chr1:99856358 | C | A | 24 | a0001c0001t0001g0257 a0001c0001t0005g0250 a0001c0001t0008g0258 others(21): Show |
25 | HG00140.hp1 HG01256.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-5145C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856358 | |||||||
chr1:99856358 | C | T | 2 | a0001c0001t0001g0213 a0008c0032t0004g0214 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.83-5145C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856358 | |||||||
chr1:99856366 | T | A | 1 | a0004c0004t0004g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.83-5137T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856366 | |||||||
chr1:99856366 | T | C | 29 | a0001c0001t0001g0242 a0001c0001t0001g0257 a0001c0001t0005g0250 others(26): Show |
30 | HG00140.hp1 HG01167.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.83-5137T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856366 | |||||||
chr1:99856370 | T | C | 1 | a0004c0004t0004g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.83-5133T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856370 | |||||||
chr1:99856374 | CCCTT | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-5125_83-5122del others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856374 | ||||||
chr1:99856419 | CTTTCT | C | 25 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-5072_83-5068del others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856419 | ||||||
chr1:99856436 | G | GTATT | 5 | a0001c0001t0007g0208 a0001c0002t0001g0043 a0001c0002t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02523.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-5045_83-5042dup others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856436 | ||||||
chr1:99856452 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(70): Show |
80 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.83-5051T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856452 | |||||||
chr1:99856476 | TGGGTGTT others(12): Show |
T | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83-5024_83-5006del others(19): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856476 | ||||||
chr1:99856518 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.83-4985A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856518 | |||||||
chr1:99856579 | A | G | 7 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-4924A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856579 | |||||||
chr1:99856699 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-4804A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856699 | |||||||
chr1:99856791 | C | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(12): Show |
16 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-4712C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856791 | |||||||
chr1:99856825 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0032 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.83-4678T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856825 | |||||||
chr1:99856890 | C | T | 3 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 |
3 | HG02717.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.83-4613C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856890 | |||||||
chr1:99856922 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-4581G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856922 | |||||||
chr1:99856935 | G | A | 1 | a0006c0008t0008g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-4568G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99856935 | |||||||
chr1:99856995 | CTCACTTC others(120): Show |
C | 2 | a0010c0011t0014g0202 a0010c0011t0014g0245 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.83-4485_83-4359del | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99856995 | ||||||
chr1:99857018 | A | T | 1 | a0024c0016t0023g0203 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.83-4485A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857018 | |||||||
chr1:99857027 | C | T | 128 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(125): Show |
140 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.83-4476C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857027 | |||||||
chr1:99857061 | G | A | 128 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(125): Show |
140 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.83-4442G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857061 | |||||||
chr1:99857064 | G | C | 1 | a0001c0001t0003g0135 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.83-4439G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857064 | |||||||
chr1:99857079 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(70): Show |
80 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.83-4424C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857079 | |||||||
chr1:99857085 | C | G | 1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-4418C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857085 | |||||||
chr1:99857090 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.83-4413C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857090 | |||||||
chr1:99857177 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(11): Show |
15 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-4326T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857177 | |||||||
chr1:99857220 | C | T | 128 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(125): Show |
140 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.83-4283C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857220 | |||||||
chr1:99857249 | C | T | 25 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-4254C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857249 | |||||||
chr1:99857270 | C | T | 3 | a0001c0022t0001g0095 a0002c0003t0006g0094 a0002c0003t0006g0096 |
3 | NA19002.hp1 NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.83-4233C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857270 | |||||||
chr1:99857337 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(11): Show |
15 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-4166C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857337 | |||||||
chr1:99857352 | C | A | 1 | a0001c0002t0018g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.83-4151C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857352 | |||||||
chr1:99857366 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83-4137G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857366 | |||||||
chr1:99857369 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-4134G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857369 | |||||||
chr1:99857373 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-4130G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857373 | |||||||
chr1:99857404 | C | CG | 10 | a0001c0001t0001g0243 a0001c0001t0001g0274 a0001c0001t0011g0226 others(7): Show |
10 | HG00423.hp2 HG00673.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.83-4095dupG | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857404 | ||||||
chr1:99857406 | G | A | 1 | a0024c0016t0023g0203 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.83-4097G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857406 | |||||||
chr1:99857412 | C | T | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-4091C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857412 | |||||||
chr1:99857421 | A | G | 1 | a0004c0004t0004g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.83-4082A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857421 | |||||||
chr1:99857461 | G | A | 1 | a0001c0001t0002g0008 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.83-4042G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857461 | |||||||
chr1:99857538 | A | G | 2 | a0001c0001t0009g0106 a0001c0001t0009g0107 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.83-3965A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857538 | |||||||
chr1:99857560 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-3943G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857560 | |||||||
chr1:99857568 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.83-3935A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857568 | |||||||
chr1:99857579 | G | A | 1 | a0005c0005t0003g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.83-3924G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857579 | |||||||
chr1:99857595 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.83-3908C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857595 | |||||||
chr1:99857634 | A | G | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.83-3869A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857634 | |||||||
chr1:99857658 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.83-3845G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857658 | |||||||
chr1:99857750 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83-3753G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857750 | |||||||
chr1:99857765 | C | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(11): Show |
15 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-3738C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857765 | |||||||
chr1:99857787 | C | CAGAGGGA others(23): Show |
68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(65): Show |
75 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.83-3696_83-3695ins others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857787 | ||||||
chr1:99857787 | C | CAGAGGGA others(23): Show |
2 | a0009c0010t0010g0205 a0009c0010t0010g0206 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.83-3696_83-3695ins others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857787 | ||||||
chr1:99857787 | C | CAGAGGGA others(24): Show |
1 | a0009c0010t0010g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83-3696_83-3695ins others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857787 | ||||||
chr1:99857787 | C | CAGAGGGA others(23): Show |
182 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(179): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.83-3686_83-3657dup others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857787 | ||||||
chr1:99857787 | C | CAGAGGGA others(24): Show |
7 | a0001c0001t0011g0174 a0001c0002t0001g0041 a0001c0002t0001g0091 others(4): Show |
7 | HG01175.hp2 HG01261.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3686_83-3685ins others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857787 | ||||||
chr1:99857798 | C | CGTGGGGA others(23): Show |
1 | a0001c0001t0003g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.83-3696_83-3695ins others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857798 | ||||||
chr1:99857799 | G | GTGGGGAG others(23): Show |
1 | a0001c0001t0003g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.83-3675_83-3674ins others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857799 | ||||||
chr1:99857800 | T | TGGGGAGG others(25): Show |
1 | a0001c0002t0022g0093 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.83-3686_83-3685ins others(32): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857800 | ||||||
chr1:99857805 | A | AGGAGGAG others(24): Show |
1 | a0002c0007t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.83-3696_83-3695ins others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857805 | ||||||
chr1:99857805 | A | AGGGGGAG others(24): Show |
1 | a0005c0005t0002g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.83-3693_83-3663dup others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857805 | ||||||
chr1:99857811 | A | AGGGGGGA others(24): Show |
3 | a0001c0001t0003g0241 a0001c0002t0001g0102 a0002c0003t0005g0089 |
3 | HG00597.hp1 HG00673.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.83-3687_83-3657dup others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857811 | ||||||
chr1:99857811 | A | AGGGGGGG others(25): Show |
2 | a0002c0003t0005g0092 a0003c0015t0012g0197 |
2 | HG01993.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.83-3686_83-3685ins others(32): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857811 | ||||||
chr1:99857831 | G | T | 1 | a0001c0001t0011g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.83-3672G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857831 | |||||||
chr1:99857834 | G | GGAGGGGG others(25): Show |
1 | a0005c0005t0002g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.83-3669_83-3668ins others(32): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857834 | |||||||
chr1:99857835 | A | AGGGGGAG others(24): Show |
3 | a0001c0014t0016g0165 a0002c0003t0005g0088 a0010c0011t0014g0245 |
3 | HG03130.hp1 HG03927.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.83-3657_83-3656ins others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857835 | ||||||
chr1:99857835 | A | G | 1 | a0005c0005t0002g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.83-3668A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857835 | |||||||
chr1:99857840 | G | T | 1 | a0001c0001t0011g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.83-3663G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857840 | |||||||
chr1:99857841 | A | AGGGGGGA others(24): Show |
1 | a0002c0003t0006g0096 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.83-3657_83-3656ins others(31): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857841 | ||||||
chr1:99857842 | G | GGGGGGAG others(22): Show |
4 | a0003c0006t0001g0175 a0003c0006t0001g0180 a0003c0006t0001g0187 others(1): Show |
4 | HG00673.hp1 HG01928.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3657_83-3656ins others(29): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857842 | ||||||
chr1:99857842 | G | GGGGGGGA others(23): Show |
1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-3657_83-3656ins others(30): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857842 | ||||||
chr1:99857843 | G | GGGGGAGA others(21): Show |
12 | a0003c0006t0001g0176 a0003c0006t0001g0177 a0003c0006t0001g0178 others(9): Show |
12 | HG00642.hp2 HG01981.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-3657_83-3656ins others(28): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857843 | ||||||
chr1:99857844 | G | GGGGAGAG others(20): Show |
2 | a0003c0006t0001g0181 a0003c0006t0001g0190 |
2 | HG02280.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.83-3657_83-3656ins others(27): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857844 | ||||||
chr1:99857846 | G | GGGAGAGG others(25): Show |
1 | a0007c0009t0004g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.83-3657_83-3656ins others(32): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857846 | |||||||
chr1:99857846 | GA | G | 3 | a0003c0006t0001g0189 a0003c0015t0012g0197 a0020c0034t0005g0196 |
3 | HG01934.hp1 HG02055.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.83-3656delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857846 | |||||||
chr1:99857847 | A | G | 20 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(17): Show |
20 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.83-3656A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857847 | |||||||
chr1:99857867 | C | T | 2 | a0006c0008t0008g0201 a0018c0027t0013g0200 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.83-3636C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857867 | |||||||
chr1:99857867 | CTCTTT | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-3627_83-3623del others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99857867 | ||||||
chr1:99857968 | C | T | 1 | a0001c0002t0008g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.83-3535C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857968 | |||||||
chr1:99857984 | A | G | 25 | a0001c0001t0001g0257 a0001c0001t0005g0250 a0001c0001t0008g0258 others(22): Show |
26 | HG00140.hp1 HG00741.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-3519A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99857984 | |||||||
chr1:99858264 | G | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3239G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99858264 | |||||||
chr1:99858908 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.83-2595C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99858908 | |||||||
chr1:99858973 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.83-2530G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99858973 | |||||||
chr1:99859182 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.83-2321A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859182 | |||||||
chr1:99859211 | C | T | 1 | a0006c0008t0008g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-2292C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859211 | |||||||
chr1:99859235 | A | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(12): Show |
16 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-2268A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859235 | |||||||
chr1:99859288 | C | G | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2215C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859288 | |||||||
chr1:99859339 | AAG | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2163_83-2162del others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859339 | |||||||
chr1:99859354 | GT | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0274 others(46): Show |
53 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.83-2139delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99859354 | ||||||
chr1:99859381 | T | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-2122T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859381 | |||||||
chr1:99859411 | C | CCT | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.83-2092_83-2091ins others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859411 | |||||||
chr1:99859433 | T | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-2070T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859433 | |||||||
chr1:99859474 | A | T | 1 | a0001c0001t0002g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.83-2029A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859474 | |||||||
chr1:99859515 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-1988G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859515 | |||||||
chr1:99859557 | AT | A | 294 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(291): Show |
315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.83-1936delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99859557 | ||||||
chr1:99859567 | T | A | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83-1936T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859567 | |||||||
chr1:99859690 | GCACACCA others(1): Show |
G | 3 | a0001c0002t0001g0086 a0002c0003t0005g0089 a0015c0021t0001g0020 |
3 | HG00621.hp1 HG02132.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.83-1806_83-1799del others(8): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 99859690 | ||||||
chr1:99859962 | T | A | 1 | a0001c0001t0005g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.83-1541T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859962 | |||||||
chr1:99859979 | T | C | 2 | a0005c0005t0002g0121 a0005c0005t0002g0122 |
2 | HG00423.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.83-1524T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859979 | |||||||
chr1:99859993 | A | C | 25 | a0001c0001t0001g0257 a0001c0001t0005g0250 a0001c0001t0008g0258 others(22): Show |
26 | HG00140.hp1 HG00741.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-1510A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99859993 | |||||||
chr1:99860181 | T | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.83-1322T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860181 | |||||||
chr1:99860314 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.83-1189G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860314 | |||||||
chr1:99860465 | T | C | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.83-1038T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860465 | |||||||
chr1:99860702 | T | C | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.83-801T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860702 | |||||||
chr1:99860707 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
6 | HG01109.hp2 HG01891.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-796A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860707 | |||||||
chr1:99860730 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.83-773G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860730 | |||||||
chr1:99860745 | C | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.83-758C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99860745 | |||||||
chr1:99861117 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-386A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861117 | |||||||
chr1:99861150 | G | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.83-353G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861150 | |||||||
chr1:99861188 | G | T | 1 | a0001c0001t0003g0224 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.83-315G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861188 | |||||||
chr1:99861240 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.83-263A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861240 | |||||||
chr1:99861256 | G | A | 2 | a0001c0001t0001g0213 a0008c0032t0004g0214 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.83-247G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861256 | |||||||
chr1:99861289 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.83-214G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861289 | |||||||
chr1:99861410 | C | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.83-93C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861410 | |||||||
chr1:99861470 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.83-33C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 2/33 | chr1 | 99861470 | |||||||
chr1:99861736 | G | A | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.293+23G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/33 | chr1 | 99861736 | |||||||
chr1:99861925 | C | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(68): Show |
81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.293+212C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/33 | chr1 | 99861925 | |||||||
chr1:99862009 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.294-248A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/33 | chr1 | 99862009 | |||||||
chr1:99862135 | T | C | 19 | a0001c0002t0005g0058 a0002c0003t0005g0022 a0002c0003t0005g0026 others(16): Show |
19 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.294-122T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/33 | chr1 | 99862135 | |||||||
chr1:99862139 | T | TAGAAATA others(325): Show |
1 | a0001c0001t0011g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294-103_294-102ins others(332): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 99862139 | ||||||
chr1:99862438 | C | T | 1 | a0004c0004t0003g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.460+15C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862438 | |||||||
chr1:99862504 | T | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.460+81T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862504 | |||||||
chr1:99862606 | A | G | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.460+183A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862606 | |||||||
chr1:99862716 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.460+293G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862716 | |||||||
chr1:99862887 | C | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.460+464C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862887 | |||||||
chr1:99862941 | TA | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(53): Show |
62 | HG00140.hp1 HG00741.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.460+527delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 99862941 | ||||||
chr1:99862950 | AT | A | 20 | a0001c0001t0001g0286 a0001c0001t0003g0013 a0001c0001t0003g0215 others(17): Show |
21 | HG00140.hp2 HG00423.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.460+539delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 99862950 | ||||||
chr1:99862951 | T | A | 2 | a0001c0001t0006g0204 a0003c0006t0001g0190 |
2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.460+528T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862951 | |||||||
chr1:99862955 | T | G | 1 | a0001c0001t0001g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.460+532T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862955 | |||||||
chr1:99862973 | A | G | 4 | a0004c0004t0004g0015 a0004c0004t0004g0262 a0004c0004t0004g0263 others(1): Show |
5 | HG03688.hp1 NA18945.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+550A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862973 | |||||||
chr1:99862986 | G | A | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.460+563G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862986 | |||||||
chr1:99862996 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.460+573A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99862996 | |||||||
chr1:99863003 | G | A | 1 | a0025c0017t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.460+580G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863003 | |||||||
chr1:99863088 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.460+665T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863088 | |||||||
chr1:99863154 | G | A | 1 | a0004c0004t0004g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.460+731G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863154 | |||||||
chr1:99863280 | A | T | 14 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(11): Show |
14 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.460+857A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863280 | |||||||
chr1:99863339 | A | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(43): Show |
54 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.460+916A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863339 | |||||||
chr1:99863378 | A | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.460+955A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863378 | |||||||
chr1:99863514 | G | T | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.461-872G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863514 | |||||||
chr1:99863517 | A | G | 2 | a0001c0001t0009g0106 a0001c0001t0009g0107 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.461-869A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863517 | |||||||
chr1:99863598 | C | T | 1 | a0001c0001t0009g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.461-788C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863598 | |||||||
chr1:99863740 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.461-646C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863740 | |||||||
chr1:99863748 | C | CT | 95 | a0001c0001t0001g0273 a0001c0001t0002g0001 a0001c0001t0002g0002 others(92): Show |
106 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.461-618dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 99863748 | ||||||
chr1:99863748 | C | CTT | 9 | a0001c0001t0002g0159 a0001c0014t0016g0133 a0004c0004t0015g0132 others(6): Show |
9 | HG00408.hp1 HG01496.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.461-619_461-618dup others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 99863748 | ||||||
chr1:99863748 | CT | C | 25 | a0001c0002t0001g0060 a0002c0003t0005g0048 a0002c0003t0005g0104 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.461-618delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 99863748 | ||||||
chr1:99863808 | C | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.461-578C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863808 | |||||||
chr1:99863879 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.461-507T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863879 | |||||||
chr1:99863907 | G | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-479G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863907 | |||||||
chr1:99863935 | C | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.461-451C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863935 | |||||||
chr1:99863977 | C | T | 1 | a0001c0001t0007g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.461-409C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99863977 | |||||||
chr1:99864007 | A | C | 1 | a0001c0001t0007g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.461-379A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864007 | |||||||
chr1:99864072 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0223 |
4 | HG02132.hp1 HG02165.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-314C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864072 | |||||||
chr1:99864107 | A | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0268 others(27): Show |
35 | HG00140.hp2 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.461-279A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864107 | |||||||
chr1:99864115 | A | G | 25 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(22): Show |
25 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.461-271A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864115 | |||||||
chr1:99864179 | A | G | 1 | a0001c0002t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.461-207A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864179 | |||||||
chr1:99864269 | G | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.461-117G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864269 | |||||||
chr1:99864333 | G | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(198): Show |
220 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.461-53G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 4/33 | chr1 | 99864333 | |||||||
chr1:99864641 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.664+52C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99864641 | |||||||
chr1:99864681 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.664+92A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99864681 | |||||||
chr1:99864739 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.664+150T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99864739 | |||||||
chr1:99865076 | T | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+487T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865076 | |||||||
chr1:99865110 | C | A | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.664+521C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865110 | |||||||
chr1:99865166 | A | AAT | 4 | a0006c0008t0008g0201 a0009c0010t0010g0206 a0018c0027t0013g0200 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+591_664+592dup others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99865166 | ||||||
chr1:99865166 | A | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(68): Show |
81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.664+577A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865166 | |||||||
chr1:99865198 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.664+609A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865198 | |||||||
chr1:99865317 | T | C | 1 | a0009c0010t0010g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.664+728T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865317 | |||||||
chr1:99865637 | A | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0222 a0001c0001t0003g0223 others(1): Show |
5 | HG02132.hp1 HG02165.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+1048A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865637 | |||||||
chr1:99865643 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.664+1054T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865643 | |||||||
chr1:99865709 | A | G | 102 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(99): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.664+1120A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865709 | |||||||
chr1:99865898 | A | G | 2 | a0006c0008t0008g0201 a0018c0027t0013g0200 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.664+1309A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865898 | |||||||
chr1:99865925 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.664+1336G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865925 | |||||||
chr1:99865994 | G | C | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.664+1405G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99865994 | |||||||
chr1:99866080 | C | T | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+1491C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866080 | |||||||
chr1:99866400 | T | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+1811T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866400 | |||||||
chr1:99866400 | T | G | 2 | a0006c0008t0007g0228 a0006c0008t0007g0239 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.664+1811T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866400 | |||||||
chr1:99866431 | C | A | 3 | a0003c0006t0001g0193 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.664+1842C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866431 | |||||||
chr1:99866589 | T | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.664+2000T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866589 | |||||||
chr1:99866659 | A | G | 3 | a0005c0005t0002g0112 a0005c0005t0002g0131 a0005c0005t0003g0130 |
3 | HG00733.hp1 HG02155.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.664+2070A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866659 | |||||||
chr1:99866677 | A | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(71): Show |
81 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.664+2088A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866677 | |||||||
chr1:99866705 | G | A | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(242): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.664+2116G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866705 | |||||||
chr1:99866762 | T | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+2173T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866762 | |||||||
chr1:99866800 | T | TTTTATTT others(5): Show |
1 | a0003c0006t0001g0184 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.664+2215_664+2226d others(14): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866800 | ||||||
chr1:99866800 | T | TTTTCTTT others(5): Show |
112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(109): Show |
123 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.664+2214_664+2215i others(14): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866800 | ||||||
chr1:99866800 | T | TTTTCTTT others(9): Show |
1 | a0005c0005t0002g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.664+2214_664+2215i others(18): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866800 | ||||||
chr1:99866800 | T | TTTTCTTT others(5): Show |
29 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(26): Show |
30 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.664+2214_664+2215i others(14): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866800 | ||||||
chr1:99866800 | T | TTTTCTTT others(5): Show |
65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(62): Show |
72 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.664+2214_664+2215i others(14): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866800 | ||||||
chr1:99866804 | A | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+2215A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866804 | |||||||
chr1:99866826 | A | AT | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.664+2246dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99866826 | ||||||
chr1:99866913 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0158 |
2 | NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.664+2324G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866913 | |||||||
chr1:99866965 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.664+2376T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99866965 | |||||||
chr1:99867062 | G | A | 2 | a0001c0001t0007g0229 a0001c0001t0007g0238 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.664+2473G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867062 | |||||||
chr1:99867197 | G | A | 1 | a0005c0005t0002g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.664+2608G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867197 | |||||||
chr1:99867429 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.664+2840G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867429 | |||||||
chr1:99867578 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.665-2822C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867578 | |||||||
chr1:99867579 | G | A | 1 | a0001c0020t0001g0023 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.665-2821G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867579 | |||||||
chr1:99867862 | A | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.665-2538A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99867862 | |||||||
chr1:99868151 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0221 |
2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.665-2249A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868151 | |||||||
chr1:99868377 | C | T | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.665-2023C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868377 | |||||||
chr1:99868484 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.665-1916C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868484 | |||||||
chr1:99868580 | C | G | 1 | a0001c0014t0016g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.665-1820C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868580 | |||||||
chr1:99868815 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665-1585G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868815 | |||||||
chr1:99868825 | C | CT | 112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(109): Show |
124 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.665-1558dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99868825 | ||||||
chr1:99868825 | CT | C | 7 | a0001c0001t0001g0268 a0001c0002t0001g0033 a0001c0002t0001g0060 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-1558delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99868825 | ||||||
chr1:99868837 | T | TG | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-1563_665-1562i others(3): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868837 | |||||||
chr1:99868868 | A | C | 1 | a0003c0006t0001g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.665-1532A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868868 | |||||||
chr1:99868960 | G | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-1440G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99868960 | |||||||
chr1:99869002 | A | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.665-1398A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869002 | |||||||
chr1:99869047 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.665-1353G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869047 | |||||||
chr1:99869137 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.665-1263T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869137 | |||||||
chr1:99869218 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1182G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869218 | |||||||
chr1:99869292 | C | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.665-1108C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869292 | |||||||
chr1:99869372 | A | AT | 3 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 |
3 | HG02717.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.665-1027dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 99869372 | ||||||
chr1:99869500 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.665-900A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869500 | |||||||
chr1:99869680 | T | C | 1 | a0001c0001t0011g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.665-720T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869680 | |||||||
chr1:99869731 | T | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.665-669T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869731 | |||||||
chr1:99869874 | G | A | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0006c0008t0008g0201 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-526G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869874 | |||||||
chr1:99869899 | A | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.665-501A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99869899 | |||||||
chr1:99870057 | C | T | 13 | a0001c0002t0001g0060 a0001c0002t0001g0062 a0001c0022t0001g0095 others(10): Show |
14 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.665-343C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99870057 | |||||||
chr1:99870070 | G | A | 12 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(9): Show |
13 | HG01256.hp2 HG01258.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.665-330G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99870070 | |||||||
chr1:99870232 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0257 others(52): Show |
61 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.665-168A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99870232 | |||||||
chr1:99870327 | A | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(91): Show |
105 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.665-73A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99870327 | |||||||
chr1:99870357 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665-43A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 5/33 | chr1 | 99870357 | |||||||
chr1:99870723 | T | C | 1 | a0016c0025t0001g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.847-35T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 6/33 | chr1 | 99870723 | |||||||
chr1:99871069 | C | T | 13 | a0001c0002t0001g0060 a0001c0002t0001g0062 a0001c0022t0001g0095 others(10): Show |
14 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.958+200C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871069 | |||||||
chr1:99871348 | G | A | 1 | a0005c0005t0003g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.958+479G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871348 | |||||||
chr1:99871364 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(12): Show |
16 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.958+495G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871364 | |||||||
chr1:99871406 | A | G | 1 | a0004c0004t0004g0262 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.958+537A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871406 | |||||||
chr1:99871410 | G | GC | 19 | a0001c0002t0001g0025 a0001c0002t0001g0039 a0001c0002t0001g0040 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.958+554dupC | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99871410 | ||||||
chr1:99871410 | GCCC | G | 184 | a0001c0001t0001g0004 a0001c0001t0001g0257 a0001c0001t0001g0268 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.958+552_958+554del others(3): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99871410 | ||||||
chr1:99871410 | GCCCC | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.958+551_958+554del others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99871410 | ||||||
chr1:99871512 | A | G | 1 | a0001c0001t0007g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.958+643A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871512 | |||||||
chr1:99871685 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.958+816T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99871685 | |||||||
chr1:99872000 | T | G | 1 | a0002c0003t0005g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.958+1131T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872000 | |||||||
chr1:99872017 | T | G | 1 | a0005c0005t0002g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.958+1148T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872017 | |||||||
chr1:99872262 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.958+1393G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872262 | |||||||
chr1:99872371 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.958+1502T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872371 | |||||||
chr1:99872483 | T | A | 1 | a0001c0002t0001g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.958+1614T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872483 | |||||||
chr1:99872490 | T | C | 1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.958+1621T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872490 | |||||||
chr1:99872499 | A | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.958+1630A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872499 | |||||||
chr1:99872534 | CT | C | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(196): Show |
218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.958+1678delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99872534 | ||||||
chr1:99872701 | G | A | 2 | a0001c0001t0007g0231 a0001c0001t0007g0232 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.958+1832G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872701 | |||||||
chr1:99872717 | C | G | 6 | a0001c0001t0005g0250 a0002c0007t0006g0266 a0004c0004t0004g0251 others(3): Show |
6 | HG01256.hp1 HG01517.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.958+1848C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872717 | |||||||
chr1:99872739 | G | C | 1 | a0001c0002t0001g0030 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.958+1870G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872739 | |||||||
chr1:99872779 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.959-1908A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872779 | |||||||
chr1:99872837 | C | A | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.959-1850C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872837 | |||||||
chr1:99872950 | T | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.959-1737T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872950 | |||||||
chr1:99872958 | C | T | 22 | a0003c0006t0001g0175 a0003c0006t0001g0176 a0003c0006t0001g0177 others(19): Show |
22 | HG00642.hp2 HG00673.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.959-1729C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872958 | |||||||
chr1:99872983 | C | A | 1 | a0005c0005t0002g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.959-1704C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99872983 | |||||||
chr1:99873036 | CA | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.959-1650delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873036 | |||||||
chr1:99873165 | T | C | 1 | a0001c0001t0002g0009 | 2 | NA18955.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.959-1522T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873165 | |||||||
chr1:99873222 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.959-1465T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873222 | |||||||
chr1:99873252 | C | T | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.959-1435C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873252 | |||||||
chr1:99873317 | T | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.959-1370T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873317 | |||||||
chr1:99873344 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.959-1343C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873344 | |||||||
chr1:99873433 | C | CT | 8 | a0001c0001t0006g0204 a0001c0001t0009g0106 a0001c0001t0009g0107 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.959-1236dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99873433 | ||||||
chr1:99873450 | T | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(12): Show |
16 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.959-1237T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873450 | |||||||
chr1:99873474 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.959-1213G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873474 | |||||||
chr1:99873505 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.959-1182A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873505 | |||||||
chr1:99873520 | C | T | 3 | a0001c0001t0003g0230 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG02683.hp2 HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.959-1167C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873520 | |||||||
chr1:99873538 | G | A | 1 | a0024c0016t0023g0203 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.959-1149G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873538 | |||||||
chr1:99873567 | T | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.959-1120T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873567 | |||||||
chr1:99873730 | G | A | 13 | a0001c0001t0003g0013 a0001c0001t0003g0215 a0001c0001t0003g0216 others(10): Show |
14 | HG01256.hp2 HG01258.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.959-957G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873730 | |||||||
chr1:99873933 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.959-754T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873933 | |||||||
chr1:99873954 | G | A | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(200): Show |
222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.959-733G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99873954 | |||||||
chr1:99874086 | A | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(93): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.959-601A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874086 | |||||||
chr1:99874103 | G | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(197): Show |
219 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.959-584G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874103 | |||||||
chr1:99874153 | C | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(202): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.959-534C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874153 | |||||||
chr1:99874250 | A | C | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(200): Show |
222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.959-437A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874250 | |||||||
chr1:99874257 | T | TA | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(199): Show |
221 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.959-418dupA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99874257 | ||||||
chr1:99874311 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.959-376A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874311 | |||||||
chr1:99874387 | T | C | 40 | a0001c0001t0001g0257 a0001c0001t0001g0268 a0001c0001t0001g0269 others(37): Show |
41 | HG00140.hp1 HG00741.hp2 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.959-300T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874387 | |||||||
chr1:99874499 | GCGTGCAC others(3): Show |
G | 2 | a0002c0003t0005g0051 a0023c0026t0009g0209 |
2 | HG00639.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.959-180_959-171del others(10): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99874499 | ||||||
chr1:99874507 | GCACGTGC others(3): Show |
G | 5 | a0001c0001t0002g0008 a0004c0004t0004g0016 a0004c0004t0004g0267 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.959-167_959-158del others(10): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99874507 | ||||||
chr1:99874517 | A | G | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-170A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874517 | |||||||
chr1:99874603 | A | G | 1 | a0002c0003t0006g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.959-84A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874603 | |||||||
chr1:99874634 | A | ATAATCTC others(61): Show |
3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.959-19_959-18insAT others(66): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 99874634 | ||||||
chr1:99874669 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(197): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.959-18G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 7/33 | chr1 | 99874669 | |||||||
chr1:99874885 | ACTT | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1082+76_1082+78del others(3): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 8/33 | chr1 | 99874885 | |||||||
chr1:99874898 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1082+88G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 8/33 | chr1 | 99874898 | |||||||
chr1:99874992 | A | G | 5 | a0003c0006t0001g0193 a0009c0010t0010g0205 a0009c0010t0010g0206 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083-162A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 8/33 | chr1 | 99874992 | |||||||
chr1:99875034 | G | C | 5 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083-120G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 8/33 | chr1 | 99875034 | |||||||
chr1:99875271 | T | C | 9 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(6): Show |
9 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185+15T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 9/33 | chr1 | 99875271 | |||||||
chr1:99875839 | AT | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1283+385delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99875839 | |||||||
chr1:99875883 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1283+428T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99875883 | |||||||
chr1:99875924 | G | T | 2 | a0003c0006t0006g0191 a0003c0006t0006g0192 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+469G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99875924 | |||||||
chr1:99875950 | T | C | 186 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(183): Show |
201 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1283+495T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99875950 | |||||||
chr1:99876053 | T | C | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284-405T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876053 | |||||||
chr1:99876055 | A | G | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284-403A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876055 | |||||||
chr1:99876106 | C | T | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1284-352C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876106 | |||||||
chr1:99876133 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1284-325C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876133 | |||||||
chr1:99876134 | G | A | 2 | a0003c0006t0006g0191 a0003c0006t0006g0192 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1284-324G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876134 | |||||||
chr1:99876235 | A | G | 1 | a0002c0003t0006g0094 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1284-223A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 10/33 | chr1 | 99876235 | |||||||
chr1:99876671 | C | T | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1423+74C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99876671 | |||||||
chr1:99876721 | G | T | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1423+124G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99876721 | |||||||
chr1:99876817 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1423+220C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99876817 | |||||||
chr1:99876860 | G | A | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1423+263G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99876860 | |||||||
chr1:99876878 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1423+281A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99876878 | |||||||
chr1:99877038 | T | C | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1423+441T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877038 | |||||||
chr1:99877091 | C | T | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1423+494C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877091 | |||||||
chr1:99877121 | G | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1424-520G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877121 | |||||||
chr1:99877213 | C | T | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424-428C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877213 | |||||||
chr1:99877228 | C | G | 1 | a0019c0029t0013g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1424-413C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877228 | |||||||
chr1:99877228 | C | T | 152 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(149): Show |
166 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1424-413C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877228 | |||||||
chr1:99877289 | G | A | 99 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(96): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1424-352G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877289 | |||||||
chr1:99877318 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1424-323T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877318 | |||||||
chr1:99877517 | T | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1424-124T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877517 | |||||||
chr1:99877597 | A | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(63): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1424-44A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877597 | |||||||
chr1:99877634 | T | A | 1 | a0003c0006t0001g0181 | 1 | HG02293.hp2 | splice_region_variant&intron_variant | LOW | c.1424-7T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 11/33 | chr1 | 99877634 | |||||||
chr1:99878222 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1611+394A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878222 | |||||||
chr1:99878237 | C | T | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1611+409C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878237 | |||||||
chr1:99878645 | C | G | 1 | a0001c0001t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1611+817C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878645 | |||||||
chr1:99878756 | T | G | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1611+928T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878756 | |||||||
chr1:99878838 | G | A | 88 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(85): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1611+1010G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878838 | |||||||
chr1:99878871 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1611+1043A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878871 | |||||||
chr1:99878940 | A | G | 41 | a0002c0003t0005g0022 a0002c0003t0005g0026 a0002c0003t0005g0045 others(38): Show |
44 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1612-983A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99878940 | |||||||
chr1:99879087 | C | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1612-836C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879087 | |||||||
chr1:99879110 | A | G | 2 | a0005c0005t0002g0123 a0005c0005t0003g0128 |
2 | NA18971.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1612-813A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879110 | |||||||
chr1:99879141 | A | T | 1 | a0007c0024t0015g0234 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1612-782A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879141 | |||||||
chr1:99879234 | A | T | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1612-689A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879234 | |||||||
chr1:99879363 | TC | T | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1612-559delC | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879363 | |||||||
chr1:99879491 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1612-432G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879491 | |||||||
chr1:99879584 | C | CAATA | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1612-317_1612-314d others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr1 | 99879584 | ||||||
chr1:99879686 | TTTC | T | 3 | a0001c0014t0016g0133 a0001c0014t0016g0165 a0001c0031t0006g0244 |
3 | HG03098.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1612-228_1612-226d others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr1 | 99879686 | ||||||
chr1:99879853 | C | G | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1612-70C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879853 | |||||||
chr1:99879899 | C | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1612-24C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 12/33 | chr1 | 99879899 | |||||||
chr1:99880269 | A | G | 3 | a0003c0006t0001g0193 a0003c0006t0008g0188 a0024c0016t0023g0203 |
3 | HG02486.hp2 HG02809.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1735+223A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 13/33 | chr1 | 99880269 | |||||||
chr1:99880310 | A | C | 2 | a0003c0006t0001g0193 a0003c0006t0008g0188 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1735+264A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 13/33 | chr1 | 99880310 | |||||||
chr1:99880419 | C | T | 43 | a0002c0003t0005g0022 a0002c0003t0005g0026 a0002c0003t0005g0045 others(40): Show |
46 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1736-213C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 13/33 | chr1 | 99880419 | |||||||
chr1:99880863 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1899+68G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 14/33 | chr1 | 99880863 | |||||||
chr1:99881185 | T | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
splice_region_variant&intron_variant | LOW | c.2001+8T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 15/33 | chr1 | 99881185 | |||||||
chr1:99881237 | A | T | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2002-55A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 15/33 | chr1 | 99881237 | |||||||
chr1:99881907 | C | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2308+216C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99881907 | |||||||
chr1:99882068 | G | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2308+377G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882068 | |||||||
chr1:99882082 | T | C | 1 | a0009c0010t0010g0205 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2308+391T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882082 | |||||||
chr1:99882136 | C | CA | 7 | a0001c0001t0001g0282 a0001c0001t0006g0204 a0001c0002t0001g0028 others(4): Show |
7 | HG01358.hp1 HG02622.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2308+464dupA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | INFO_REALIGN_3_PRIME | chr1 | 99882136 | ||||||
chr1:99882142 | AAAAAAAA others(7): Show |
A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2308+455_2308+468d others(16): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | INFO_REALIGN_3_PRIME | chr1 | 99882142 | ||||||
chr1:99882156 | G | A | 24 | a0001c0001t0006g0204 a0001c0031t0006g0244 a0003c0006t0006g0191 others(21): Show |
25 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.2308+465G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882156 | |||||||
chr1:99882378 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0236 |
2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2308+687C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882378 | |||||||
chr1:99882392 | C | G | 2 | a0003c0006t0001g0193 a0003c0006t0008g0188 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2308+701C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882392 | |||||||
chr1:99882400 | C | A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0278 a0001c0001t0001g0290 others(1): Show |
4 | NA18956.hp2 NA19005.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2308+709C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882400 | |||||||
chr1:99882419 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2308+728A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882419 | |||||||
chr1:99882471 | G | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2308+780G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882471 | |||||||
chr1:99882765 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2308+1074A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882765 | |||||||
chr1:99882834 | A | G | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2308+1143A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882834 | |||||||
chr1:99882991 | T | A | 1 | a0001c0002t0018g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2309-1129T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99882991 | |||||||
chr1:99883017 | T | G | 2 | a0001c0001t0002g0134 a0001c0001t0002g0158 |
2 | NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2309-1103T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883017 | |||||||
chr1:99883027 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2309-1093A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883027 | |||||||
chr1:99883099 | C | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2309-1021C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883099 | |||||||
chr1:99883633 | T | A | 7 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(4): Show |
7 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2309-487T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883633 | |||||||
chr1:99883656 | A | G | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2309-464A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883656 | |||||||
chr1:99883670 | G | C | 8 | a0003c0006t0001g0175 a0003c0006t0001g0179 a0003c0006t0001g0180 others(5): Show |
8 | HG00673.hp1 HG01928.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.2309-450G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883670 | |||||||
chr1:99883825 | A | C | 88 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(85): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2309-295A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 17/33 | chr1 | 99883825 | |||||||
chr1:99884761 | C | T | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2681+58C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99884761 | |||||||
chr1:99884827 | G | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2681+124G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99884827 | |||||||
chr1:99884909 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2681+206A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99884909 | |||||||
chr1:99885127 | G | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2681+424G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885127 | |||||||
chr1:99885436 | A | G | 1 | a0015c0021t0001g0020 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2681+733A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885436 | |||||||
chr1:99885455 | C | T | 2 | a0001c0014t0016g0133 a0001c0014t0016g0165 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2681+752C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885455 | |||||||
chr1:99885512 | C | G | 1 | a0018c0027t0013g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2681+809C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885512 | |||||||
chr1:99885636 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2681+933T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885636 | |||||||
chr1:99885704 | T | G | 7 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(4): Show |
7 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2681+1001T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885704 | |||||||
chr1:99885899 | G | A | 7 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(4): Show |
7 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2681+1196G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885899 | |||||||
chr1:99885965 | A | G | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2681+1262A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99885965 | |||||||
chr1:99886079 | G | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2681+1376G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886079 | |||||||
chr1:99886097 | T | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2681+1394T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886097 | |||||||
chr1:99886106 | G | A | 2 | a0001c0014t0016g0133 a0001c0014t0016g0165 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2681+1403G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886106 | |||||||
chr1:99886128 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2681+1425A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886128 | |||||||
chr1:99886147 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2681+1444A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886147 | |||||||
chr1:99886159 | T | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2681+1456T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886159 | |||||||
chr1:99886233 | T | C | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2681+1530T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886233 | |||||||
chr1:99886254 | T | C | 11 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(8): Show |
11 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2681+1551T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886254 | |||||||
chr1:99886296 | T | A | 1 | a0007c0024t0015g0234 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2681+1593T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886296 | |||||||
chr1:99886387 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2682-1591C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886387 | |||||||
chr1:99886487 | GA | G | 159 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(156): Show |
173 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.2682-1480delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 99886487 | ||||||
chr1:99886542 | C | G | 1 | a0001c0002t0001g0085 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2682-1436C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886542 | |||||||
chr1:99886623 | A | G | 1 | a0019c0029t0013g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2682-1355A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886623 | |||||||
chr1:99886730 | T | C | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2682-1248T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886730 | |||||||
chr1:99886794 | T | C | 5 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2682-1184T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886794 | |||||||
chr1:99886914 | C | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2682-1064C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99886914 | |||||||
chr1:99887160 | G | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2682-818G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99887160 | |||||||
chr1:99887200 | A | G | 192 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(189): Show |
207 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.2682-778A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99887200 | |||||||
chr1:99887418 | A | G | 2 | a0018c0027t0013g0200 a0019c0029t0013g0212 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2682-560A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99887418 | |||||||
chr1:99887463 | T | C | 186 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(183): Show |
201 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2682-515T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99887463 | |||||||
chr1:99887939 | A | T | 1 | a0019c0029t0013g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2682-39A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 20/33 | chr1 | 99887939 | |||||||
chr1:99888119 | G | A | 186 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(183): Show |
201 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2812+11G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888119 | |||||||
chr1:99888204 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2812+96A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888204 | |||||||
chr1:99888463 | C | G | 1 | a0001c0001t0007g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2812+355C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888463 | |||||||
chr1:99888744 | A | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0167 |
2 | NA18945.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2812+636A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888744 | |||||||
chr1:99888812 | T | G | 2 | a0008c0013t0004g0063 a0008c0032t0004g0214 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2812+704T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888812 | |||||||
chr1:99888851 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2812+743C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888851 | |||||||
chr1:99888974 | A | G | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2812+866A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99888974 | |||||||
chr1:99889047 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2812+939G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889047 | |||||||
chr1:99889078 | A | G | 9 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(6): Show |
9 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2812+970A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889078 | |||||||
chr1:99889092 | C | CCA | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2812+985_2812+986i others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99889092 | ||||||
chr1:99889106 | A | G | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2812+998A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889106 | |||||||
chr1:99889118 | G | T | 1 | a0001c0001t0007g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2812+1010G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889118 | |||||||
chr1:99889236 | T | C | 2 | a0001c0001t0001g0257 a0001c0002t0001g0074 |
2 | HG03490.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2812+1128T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889236 | |||||||
chr1:99889312 | C | T | 4 | a0006c0008t0007g0228 a0006c0008t0007g0239 a0006c0008t0008g0018 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2812+1204C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889312 | |||||||
chr1:99889625 | G | A | 1 | a0009c0010t0010g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2812+1517G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889625 | |||||||
chr1:99889708 | C | T | 21 | a0001c0001t0003g0014 a0001c0001t0003g0120 a0001c0001t0003g0225 others(18): Show |
23 | HG00597.hp1 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2813-1512C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99889708 | |||||||
chr1:99890004 | G | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.2813-1216G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890004 | |||||||
chr1:99890241 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2813-979A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890241 | |||||||
chr1:99890343 | C | T | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2813-877C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890343 | |||||||
chr1:99890347 | G | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-873G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890347 | |||||||
chr1:99890349 | A | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-871A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890349 | |||||||
chr1:99890351 | A | G | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-869A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890351 | |||||||
chr1:99890353 | G | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-867G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890353 | |||||||
chr1:99890354 | T | TCCCA | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-866_2813-865i others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890354 | |||||||
chr1:99890356 | G | C | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-864G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890356 | |||||||
chr1:99890358 | A | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-862A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890358 | |||||||
chr1:99890359 | T | C | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-861T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890359 | |||||||
chr1:99890360 | A | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-860A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890360 | |||||||
chr1:99890365 | T | G | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-855T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890365 | |||||||
chr1:99890368 | A | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-852A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890368 | |||||||
chr1:99890370 | A | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-850A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890370 | |||||||
chr1:99890371 | G | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-849G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890371 | |||||||
chr1:99890373 | C | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-847C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890373 | |||||||
chr1:99890376 | G | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-844G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890376 | |||||||
chr1:99890378 | T | TTTTTTTT others(222): Show |
2 | a0002c0003t0006g0064 a0002c0007t0006g0266 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2813-841_2813-840i others(231): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890378 | ||||||
chr1:99890378 | T | TTTTTTTT others(224): Show |
1 | a0002c0003t0006g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2813-841_2813-840i others(233): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890378 | ||||||
chr1:99890378 | T | TTTTTTTT others(229): Show |
1 | a0002c0003t0021g0061 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2813-841_2813-840i others(238): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890378 | ||||||
chr1:99890378 | T | TTTTTTTT others(235): Show |
1 | a0002c0003t0006g0066 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2813-841_2813-840i others(244): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890378 | ||||||
chr1:99890381 | C | T | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-839C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890381 | |||||||
chr1:99890383 | A | G | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-837A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890383 | |||||||
chr1:99890384 | A | ATC | 5 | a0002c0003t0006g0064 a0002c0003t0006g0065 a0002c0003t0006g0066 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2813-836_2813-835i others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890384 | |||||||
chr1:99890462 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2813-758A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890462 | |||||||
chr1:99890540 | A | T | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2813-680A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890540 | |||||||
chr1:99890641 | GA | G | 30 | a0001c0001t0003g0014 a0001c0001t0003g0230 a0001c0001t0003g0233 others(27): Show |
32 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.2813-569delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890641 | ||||||
chr1:99890641 | GAA | G | 7 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(4): Show |
7 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2813-570_2813-569d others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890641 | ||||||
chr1:99890641 | GAAA | G | 13 | a0001c0001t0002g0117 a0001c0001t0002g0295 a0002c0003t0006g0064 others(10): Show |
14 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.2813-571_2813-569d others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890641 | ||||||
chr1:99890648 | A | T | 30 | a0001c0001t0003g0014 a0001c0001t0003g0230 a0001c0001t0003g0233 others(27): Show |
32 | HG00140.hp1 HG00597.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.2813-572A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890648 | |||||||
chr1:99890649 | AAAT | A | 126 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(123): Show |
138 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.2813-569_2813-567d others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 99890649 | ||||||
chr1:99890650 | A | AT | 4 | a0001c0001t0001g0276 a0003c0006t0008g0188 a0003c0015t0012g0195 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813-570_2813-569i others(3): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890650 | |||||||
chr1:99890650 | A | T | 39 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(36): Show |
41 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.2813-570A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890650 | |||||||
chr1:99890651 | ATAT | A | 4 | a0001c0001t0002g0113 a0001c0001t0002g0138 a0001c0001t0002g0159 others(1): Show |
4 | HG00408.hp1 HG02155.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813-568_2813-566d others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890651 | |||||||
chr1:99890652 | T | A | 5 | a0001c0001t0006g0204 a0001c0002t0001g0073 a0003c0006t0001g0194 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2813-568T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890652 | |||||||
chr1:99890931 | C | G | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2813-289C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99890931 | |||||||
chr1:99891043 | T | C | 2 | a0018c0027t0013g0200 a0019c0029t0013g0212 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2813-177T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99891043 | |||||||
chr1:99891110 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(8): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2813-110C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99891110 | |||||||
chr1:99891117 | A | C | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2813-103A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99891117 | |||||||
chr1:99891197 | A | G | 1 | a0019c0029t0013g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2813-23A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 21/33 | chr1 | 99891197 | |||||||
chr1:99891485 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2950-121A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 22/33 | chr1 | 99891485 | |||||||
chr1:99891585 | T | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.2950-21T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 22/33 | chr1 | 99891585 | |||||||
chr1:99891791 | A | G | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3083+52A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 23/33 | chr1 | 99891791 | |||||||
chr1:99891823 | C | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3083+84C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 23/33 | chr1 | 99891823 | |||||||
chr1:99892046 | T | A | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3083+307T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 23/33 | chr1 | 99892046 | |||||||
chr1:99892424 | T | C | 1 | a0015c0021t0001g0020 | 1 | HG02132.hp2 | splice_region_variant&intron_variant | LOW | c.3084-8T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 23/33 | chr1 | 99892424 | |||||||
chr1:99892633 | A | G | 1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3259+26A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892633 | |||||||
chr1:99892644 | G | A | 187 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(184): Show |
202 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3259+37G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892644 | |||||||
chr1:99892656 | G | A | 2 | a0008c0013t0004g0063 a0008c0032t0004g0214 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3259+49G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892656 | |||||||
chr1:99892771 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3259+164C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892771 | |||||||
chr1:99892830 | A | ATTCTT | 160 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(157): Show |
174 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.3259+224_3259+228d others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 99892830 | ||||||
chr1:99892895 | G | A | 192 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(189): Show |
207 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.3259+288G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892895 | |||||||
chr1:99892944 | C | A | 1 | a0001c0001t0002g0160 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3259+337C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99892944 | |||||||
chr1:99893251 | A | G | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3259+644A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893251 | |||||||
chr1:99893600 | T | C | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+993T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893600 | |||||||
chr1:99893646 | G | A | 23 | a0004c0004t0003g0240 a0004c0004t0004g0015 a0004c0004t0004g0016 others(20): Show |
24 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.3259+1039G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893646 | |||||||
chr1:99893656 | T | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.3259+1049T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893656 | |||||||
chr1:99893714 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3259+1107A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893714 | |||||||
chr1:99893722 | G | A | 4 | a0002c0003t0005g0045 a0002c0003t0005g0050 a0002c0003t0005g0056 others(1): Show |
4 | NA18612.hp2 NA19066.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+1115G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893722 | |||||||
chr1:99893777 | A | G | 235 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(232): Show |
255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.3259+1170A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99893777 | |||||||
chr1:99894186 | C | CA | 6 | a0001c0001t0002g0172 a0001c0002t0001g0030 a0001c0002t0001g0072 others(3): Show |
6 | HG01070.hp1 HG01433.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.3259+1594dupA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 99894186 | ||||||
chr1:99894279 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3259+1672G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894279 | |||||||
chr1:99894309 | C | T | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.3259+1702C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894309 | |||||||
chr1:99894618 | A | G | 1 | a0002c0003t0005g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3260-1668A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894618 | |||||||
chr1:99894655 | AAACT | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3260-1627_3260-162 others(8): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 99894655 | ||||||
chr1:99894663 | A | G | 1 | a0016c0025t0001g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3260-1623A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894663 | |||||||
chr1:99894761 | A | G | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3260-1525A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894761 | |||||||
chr1:99894817 | A | G | 3 | a0004c0004t0004g0017 a0004c0004t0004g0249 a0022c0023t0004g0017 |
3 | HG03579.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3260-1469A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894817 | |||||||
chr1:99894835 | A | G | 153 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(150): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.3260-1451A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894835 | |||||||
chr1:99894861 | G | A | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3260-1425G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99894861 | |||||||
chr1:99895009 | T | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3260-1277T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99895009 | |||||||
chr1:99895078 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3260-1208C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99895078 | |||||||
chr1:99895163 | C | T | 1 | a0005c0005t0003g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3260-1123C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99895163 | |||||||
chr1:99895375 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3260-911A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99895375 | |||||||
chr1:99896022 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3260-264A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99896022 | |||||||
chr1:99896213 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3260-73A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99896213 | |||||||
chr1:99896267 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3260-19G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 24/33 | chr1 | 99896267 | |||||||
chr1:99896403 | A | G | 1 | a0005c0018t0005g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3362+15A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896403 | |||||||
chr1:99896410 | T | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3362+22T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896410 | |||||||
chr1:99896624 | G | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.3362+236G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896624 | |||||||
chr1:99896637 | T | C | 1 | a0003c0006t0001g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3362+249T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896637 | |||||||
chr1:99896794 | G | GT | 9 | a0001c0001t0001g0281 a0001c0002t0001g0081 a0002c0003t0005g0026 others(6): Show |
9 | HG01934.hp1 HG01981.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3362+414dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99896794 | ||||||
chr1:99896833 | CAG | C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0233 a0001c0001t0003g0237 |
4 | HG02698.hp1 HG03491.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3362+448_3362+449d others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99896833 | ||||||
chr1:99896841 | C | T | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3362+453C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896841 | |||||||
chr1:99896849 | C | T | 1 | a0003c0006t0001g0189 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3362+461C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896849 | |||||||
chr1:99896854 | G | A | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3362+466G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896854 | |||||||
chr1:99896879 | C | T | 4 | a0001c0001t0006g0204 a0001c0031t0006g0244 a0003c0006t0006g0191 others(1): Show |
4 | HG02622.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3362+491C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896879 | |||||||
chr1:99896910 | G | A | 1 | a0001c0001t0007g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3362+522G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896910 | |||||||
chr1:99896974 | G | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3362+586G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99896974 | |||||||
chr1:99897004 | A | G | 2 | a0003c0006t0001g0193 a0003c0006t0008g0188 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3362+616A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897004 | |||||||
chr1:99897095 | G | A | 11 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(8): Show |
11 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.3362+707G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897095 | |||||||
chr1:99897170 | G | A | 2 | a0003c0006t0001g0193 a0003c0006t0008g0188 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3362+782G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897170 | |||||||
chr1:99897431 | A | G | 1 | a0005c0005t0002g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3362+1043A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897431 | |||||||
chr1:99897434 | A | G | 1 | a0005c0018t0005g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3362+1046A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897434 | |||||||
chr1:99897449 | G | A | 2 | a0018c0027t0013g0200 a0019c0029t0013g0212 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3362+1061G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897449 | |||||||
chr1:99897476 | A | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(86): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3362+1088A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897476 | |||||||
chr1:99897678 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0080 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3362+1290C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99897678 | |||||||
chr1:99898049 | C | CT | 24 | a0001c0001t0003g0170 a0001c0002t0005g0058 a0004c0004t0003g0240 others(21): Show |
25 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.3362+1676dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99898049 | ||||||
chr1:99898049 | CT | C | 46 | a0001c0001t0002g0157 a0001c0001t0003g0233 a0001c0002t0001g0041 others(43): Show |
49 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.3362+1676delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99898049 | ||||||
chr1:99898113 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3362+1725C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898113 | |||||||
chr1:99898147 | T | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(67): Show |
78 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3362+1759T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898147 | |||||||
chr1:99898191 | C | T | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3362+1803C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898191 | |||||||
chr1:99898476 | C | A | 2 | a0001c0001t0002g0173 a0001c0001t0003g0135 |
2 | HG02080.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.3362+2088C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898476 | |||||||
chr1:99898644 | A | G | 1 | a0010c0011t0014g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3363-1992A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898644 | |||||||
chr1:99898645 | T | C | 178 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(175): Show |
192 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.3363-1991T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99898645 | |||||||
chr1:99899063 | G | A | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3363-1573G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899063 | |||||||
chr1:99899078 | CAAATATA others(13): Show |
C | 14 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0278 others(11): Show |
15 | HG00438.hp1 NA18949.hp1 NA18956.hp2 others(12): Show |
intron_variant | MODIFIER | c.3363-1556_3363-153 others(24): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899078 | ||||||
chr1:99899089 | G | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3363-1547G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899089 | |||||||
chr1:99899091 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3363-1545A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899091 | |||||||
chr1:99899226 | A | T | 11 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(8): Show |
11 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.3363-1410A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899226 | |||||||
chr1:99899452 | AGTTTTTA others(12): Show |
A | 1 | a0001c0002t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3363-1183_3363-116 others(23): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899452 | |||||||
chr1:99899476 | T | G | 1 | a0001c0001t0002g0139 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3363-1160T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899476 | |||||||
chr1:99899518 | CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3363-1094_3363-108 others(16): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899518 | ||||||
chr1:99899522 | C | T | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3363-1114C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899522 | |||||||
chr1:99899524 | C | CTCTT | 104 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(101): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.3363-1109_3363-110 others(8): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899524 | ||||||
chr1:99899528 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3363-1108C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899528 | |||||||
chr1:99899528 | CTT | C | 5 | a0001c0001t0006g0204 a0002c0003t0006g0064 a0002c0007t0006g0266 others(2): Show |
5 | HG02602.hp1 HG02622.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.3363-1106_3363-110 others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899528 | ||||||
chr1:99899530 | T | C | 147 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(144): Show |
160 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.3363-1106T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899530 | |||||||
chr1:99899530 | T | TTC | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0242 others(54): Show |
63 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.3363-1096_3363-109 others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899530 | ||||||
chr1:99899530 | T | TTCTCTC | 23 | a0001c0031t0006g0244 a0004c0004t0004g0015 a0004c0004t0004g0016 others(20): Show |
24 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.3363-1100_3363-109 others(10): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899530 | ||||||
chr1:99899542 | T | C | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3363-1094T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899542 | |||||||
chr1:99899606 | TTTCC | T | 4 | a0001c0002t0001g0032 a0001c0002t0001g0060 a0001c0002t0001g0062 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363-1026_3363-102 others(8): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 99899606 | ||||||
chr1:99899725 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3363-911G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899725 | |||||||
chr1:99899781 | C | T | 1 | a0005c0005t0002g0123 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3363-855C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899781 | |||||||
chr1:99899826 | T | A | 1 | a0003c0006t0001g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3363-810T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899826 | |||||||
chr1:99899841 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3363-795C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899841 | |||||||
chr1:99899895 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3363-741C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899895 | |||||||
chr1:99899907 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
7 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363-729A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99899907 | |||||||
chr1:99900004 | A | G | 2 | a0001c0001t0003g0215 a0001c0001t0003g0218 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3363-632A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900004 | |||||||
chr1:99900042 | G | T | 1 | a0001c0001t0001g0280 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3363-594G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900042 | |||||||
chr1:99900064 | G | A | 1 | a0007c0009t0004g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3363-572G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900064 | |||||||
chr1:99900121 | C | G | 144 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(141): Show |
157 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.3363-515C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900121 | |||||||
chr1:99900241 | C | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(174): Show |
191 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.3363-395C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900241 | |||||||
chr1:99900292 | T | C | 9 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(6): Show |
9 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.3363-344T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900292 | |||||||
chr1:99900293 | G | A | 7 | a0001c0001t0003g0014 a0001c0001t0003g0230 a0001c0001t0003g0233 others(4): Show |
8 | HG00597.hp1 HG02683.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.3363-343G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900293 | |||||||
chr1:99900585 | A | G | 6 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 others(3): Show |
6 | HG01167.hp2 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3363-51A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 25/33 | chr1 | 99900585 | |||||||
chr1:99900882 | G | GT | 2 | a0001c0001t0001g0004 a0001c0001t0001g0271 |
4 | NA18947.hp2 NA18983.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.3588+28dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99900882 | ||||||
chr1:99900890 | G | GT | 15 | a0001c0001t0001g0257 a0001c0001t0001g0280 a0001c0001t0003g0120 others(12): Show |
17 | HG00642.hp2 HG01069.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.3588+44dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99900890 | ||||||
chr1:99900890 | G | T | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3588+29G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99900890 | |||||||
chr1:99900890 | GT | G | 9 | a0001c0002t0001g0041 a0001c0014t0016g0133 a0001c0014t0016g0165 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3588+44delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99900890 | ||||||
chr1:99900890 | GTT | G | 113 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(110): Show |
124 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3588+43_3588+44del others(2): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99900890 | ||||||
chr1:99900897 | T | G | 6 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 others(3): Show |
6 | HG01167.hp2 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3588+36T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99900897 | |||||||
chr1:99901382 | T | TA | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0213 others(101): Show |
114 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.3588+544dupA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99901382 | ||||||
chr1:99901382 | TA | T | 60 | a0001c0001t0003g0129 a0001c0001t0003g0216 a0001c0001t0003g0217 others(57): Show |
63 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.3588+544delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99901382 | ||||||
chr1:99901382 | TAA | T | 29 | a0001c0001t0006g0204 a0002c0003t0005g0045 a0002c0003t0005g0048 others(26): Show |
30 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3588+543_3588+544d others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99901382 | ||||||
chr1:99901388 | A | G | 1 | a0001c0002t0001g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3588+527A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99901388 | |||||||
chr1:99901408 | G | A | 1 | a0005c0005t0002g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3588+547G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99901408 | |||||||
chr1:99901426 | T | G | 1 | a0001c0001t0007g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3588+565T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99901426 | |||||||
chr1:99901523 | A | G | 1 | a0003c0006t0001g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3588+662A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99901523 | |||||||
chr1:99901759 | AT | A | 4 | a0001c0001t0002g0138 a0004c0004t0004g0015 a0004c0004t0004g0263 others(1): Show |
5 | NA18945.hp2 NA18980.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.3588+900delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99901759 | ||||||
chr1:99901823 | T | C | 138 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(135): Show |
151 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.3589-860T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99901823 | |||||||
chr1:99901830 | ATATT | A | 8 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(5): Show |
8 | HG01261.hp1 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.3589-845_3589-842d others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99901830 | ||||||
chr1:99902018 | ATAG | A | 7 | a0007c0009t0004g0054 a0007c0009t0004g0071 a0007c0009t0004g0090 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3589-661_3589-659d others(5): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 99902018 | ||||||
chr1:99902024 | G | T | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3589-659G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902024 | |||||||
chr1:99902085 | A | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3589-598A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902085 | |||||||
chr1:99902223 | C | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3589-460C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902223 | |||||||
chr1:99902268 | A | G | 3 | a0008c0013t0004g0019 a0008c0013t0004g0063 a0008c0032t0004g0214 |
3 | HG02630.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3589-415A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902268 | |||||||
chr1:99902318 | G | A | 1 | a0001c0002t0001g0046 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3589-365G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902318 | |||||||
chr1:99902335 | G | A | 22 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(19): Show |
23 | HG00733.hp2 HG01069.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.3589-348G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902335 | |||||||
chr1:99902449 | C | A | 1 | a0001c0001t0003g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3589-234C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902449 | |||||||
chr1:99902651 | A | G | 2 | a0004c0004t0004g0256 a0004c0004t0004g0265 |
2 | NA18971.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.3589-32A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 26/33 | chr1 | 99902651 | |||||||
chr1:99902826 | T | C | 19 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(16): Show |
20 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.3700+32T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99902826 | |||||||
chr1:99902968 | A | C | 1 | a0001c0001t0003g0224 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3700+174A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99902968 | |||||||
chr1:99903030 | G | A | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3700+236G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903030 | |||||||
chr1:99903041 | C | T | 1 | a0005c0005t0002g0171 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3700+247C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903041 | |||||||
chr1:99903084 | A | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(106): Show |
120 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.3700+290A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903084 | |||||||
chr1:99903145 | T | A | 2 | a0002c0003t0006g0068 a0002c0003t0006g0097 |
2 | NA18953.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3700+351T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903145 | |||||||
chr1:99903233 | C | T | 1 | a0020c0034t0005g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3700+439C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903233 | |||||||
chr1:99903245 | T | C | 1 | a0001c0002t0005g0058 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3700+451T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903245 | |||||||
chr1:99903282 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3700+488C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903282 | |||||||
chr1:99903332 | G | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.3700+538G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903332 | |||||||
chr1:99903355 | A | T | 1 | a0001c0002t0001g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3700+561A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903355 | |||||||
chr1:99903509 | A | C | 8 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(5): Show |
8 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.3700+715A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903509 | |||||||
chr1:99903538 | A | G | 1 | a0019c0029t0013g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3700+744A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903538 | |||||||
chr1:99903557 | C | G | 1 | a0001c0002t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3700+763C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903557 | |||||||
chr1:99903570 | A | G | 2 | a0001c0014t0016g0133 a0001c0014t0016g0165 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3700+776A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903570 | |||||||
chr1:99903721 | A | G | 4 | a0004c0004t0004g0016 a0004c0004t0004g0267 a0004c0004t0015g0132 others(1): Show |
4 | HG00741.hp2 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.3700+927A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903721 | |||||||
chr1:99903742 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3700+948A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903742 | |||||||
chr1:99903773 | T | A | 1 | a0018c0027t0013g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3700+979T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903773 | |||||||
chr1:99903821 | T | C | 131 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(128): Show |
143 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.3700+1027T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903821 | |||||||
chr1:99903835 | G | T | 2 | a0010c0011t0014g0202 a0010c0011t0014g0245 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3700+1041G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903835 | |||||||
chr1:99903991 | G | A | 16 | a0001c0002t0006g0042 a0002c0003t0006g0064 a0002c0003t0006g0065 others(13): Show |
17 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.3700+1197G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99903991 | |||||||
chr1:99904182 | G | A | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3700+1388G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904182 | |||||||
chr1:99904206 | G | A | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3700+1412G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904206 | |||||||
chr1:99904208 | C | T | 1 | a0014c0019t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3700+1414C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904208 | |||||||
chr1:99904432 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3700+1638T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904432 | |||||||
chr1:99904504 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3700+1710G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904504 | |||||||
chr1:99904552 | A | G | 2 | a0001c0001t0007g0231 a0001c0001t0007g0232 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3700+1758A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904552 | |||||||
chr1:99904578 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3700+1784A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904578 | |||||||
chr1:99904695 | T | C | 1 | a0002c0003t0005g0052 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3700+1901T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904695 | |||||||
chr1:99904748 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0080 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3700+1954C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904748 | |||||||
chr1:99904780 | C | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3700+1986C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904780 | |||||||
chr1:99904839 | C | G | 1 | a0001c0001t0011g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3700+2045C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904839 | |||||||
chr1:99904879 | G | C | 1 | a0003c0006t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3700+2085G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904879 | |||||||
chr1:99904930 | G | A | 163 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(160): Show |
176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3700+2136G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99904930 | |||||||
chr1:99905046 | T | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3700+2252T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905046 | |||||||
chr1:99905167 | G | T | 7 | a0007c0009t0004g0054 a0007c0009t0004g0071 a0007c0009t0004g0090 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3700+2373G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905167 | |||||||
chr1:99905277 | A | C | 19 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(16): Show |
20 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.3700+2483A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905277 | |||||||
chr1:99905302 | T | G | 1 | a0001c0001t0007g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3700+2508T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905302 | |||||||
chr1:99905372 | T | TTTG | 12 | a0001c0001t0002g0117 a0001c0001t0002g0141 a0001c0001t0003g0170 others(9): Show |
12 | HG01175.hp1 HG02071.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.3700+2614_3700+261 others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905372 | ||||||
chr1:99905372 | T | TTTGTTG | 6 | a0001c0001t0001g0271 a0003c0006t0001g0182 a0003c0006t0001g0193 others(3): Show |
6 | HG01167.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3700+2611_3700+261 others(10): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905372 | ||||||
chr1:99905372 | T | TTTGTTGT others(2): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
7 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3700+2608_3700+261 others(13): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905372 | ||||||
chr1:99905372 | TTTG | T | 6 | a0001c0001t0002g0147 a0001c0001t0009g0106 a0001c0001t0009g0107 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.3700+2614_3700+261 others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905372 | ||||||
chr1:99905372 | TTTGTTG | T | 31 | a0002c0003t0006g0065 a0004c0004t0004g0015 a0004c0004t0004g0016 others(28): Show |
32 | HG00140.hp1 HG00733.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.3700+2611_3700+261 others(10): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905372 | ||||||
chr1:99905512 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3700+2718C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905512 | |||||||
chr1:99905518 | G | T | 163 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(160): Show |
176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3700+2724G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905518 | |||||||
chr1:99905531 | C | T | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3700+2737C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905531 | |||||||
chr1:99905536 | T | G | 1 | a0001c0022t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3700+2742T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905536 | |||||||
chr1:99905654 | A | G | 1 | a0003c0006t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3700+2860A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905654 | |||||||
chr1:99905811 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3700+3017C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99905811 | |||||||
chr1:99905920 | T | TTTTTG | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3700+3146_3700+315 others(9): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99905920 | ||||||
chr1:99906015 | A | G | 7 | a0007c0009t0004g0054 a0007c0009t0004g0071 a0007c0009t0004g0090 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3700+3221A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906015 | |||||||
chr1:99906056 | C | G | 8 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0219 others(5): Show |
8 | HG01257.hp2 HG01261.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.3700+3262C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906056 | |||||||
chr1:99906116 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3700+3322A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906116 | |||||||
chr1:99906194 | A | G | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3700+3400A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906194 | |||||||
chr1:99906219 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3700+3425G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906219 | |||||||
chr1:99906499 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3700+3705A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906499 | |||||||
chr1:99906509 | C | T | 12 | a0001c0001t0007g0208 a0001c0001t0007g0227 a0001c0001t0007g0229 others(9): Show |
13 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3700+3715C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906509 | |||||||
chr1:99906561 | T | C | 2 | a0010c0011t0014g0202 a0010c0011t0014g0245 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3700+3767T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906561 | |||||||
chr1:99906621 | G | A | 6 | a0005c0005t0002g0109 a0005c0005t0002g0110 a0005c0005t0002g0124 others(3): Show |
6 | HG01993.hp1 NA18948.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3700+3827G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906621 | |||||||
chr1:99906686 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.3700+3892C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906686 | |||||||
chr1:99906717 | T | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.3700+3923T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99906717 | |||||||
chr1:99907031 | G | T | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3701-3681G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907031 | |||||||
chr1:99907061 | G | A | 1 | a0005c0005t0003g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3701-3651G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907061 | |||||||
chr1:99907072 | T | G | 1 | a0001c0002t0001g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3701-3640T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907072 | |||||||
chr1:99907302 | G | A | 22 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(19): Show |
23 | HG00733.hp2 HG01069.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.3701-3410G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907302 | |||||||
chr1:99907433 | T | C | 1 | a0002c0003t0006g0094 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3701-3279T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907433 | |||||||
chr1:99907486 | G | A | 1 | a0004c0004t0004g0253 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3701-3226G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907486 | |||||||
chr1:99907496 | T | A | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3701-3216T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907496 | |||||||
chr1:99907676 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3701-3036G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907676 | |||||||
chr1:99907680 | G | GTTTTTTT others(5): Show |
1 | a0001c0014t0016g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3701-3027_3701-302 others(16): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907680 | ||||||
chr1:99907686 | G | GTTTTTTT others(6): Show |
1 | a0001c0014t0016g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3701-3020_3701-301 others(17): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907686 | ||||||
chr1:99907686 | G | T | 1 | a0001c0014t0016g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3701-3026G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907686 | |||||||
chr1:99907693 | G | GTTTTTTG others(7): Show |
6 | a0001c0002t0008g0087 a0003c0015t0012g0195 a0003c0015t0012g0197 others(3): Show |
6 | HG01167.hp2 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-3013_3701-301 others(18): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTG others(8): Show |
1 | a0002c0003t0005g0022 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3701-3013_3701-301 others(19): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTG others(9): Show |
6 | a0001c0001t0009g0106 a0001c0001t0011g0114 a0001c0001t0011g0174 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-3013_3701-301 others(20): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTG others(10): Show |
1 | a0001c0001t0009g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3701-3013_3701-301 others(21): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(9): Show |
21 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(18): Show |
22 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3701-3010_3701-300 others(20): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(10): Show |
1 | a0004c0004t0004g0253 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3701-3010_3701-300 others(21): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0243 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(17): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(7): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0213 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(18): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(7): Show |
6 | a0007c0009t0004g0054 a0007c0009t0004g0090 a0007c0024t0015g0234 others(3): Show |
6 | HG02071.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(18): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(8): Show |
1 | a0007c0009t0004g0071 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3701-3011_3701-301 others(19): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3701-3011_3701-301 others(17): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(7): Show |
76 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(73): Show |
85 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(18): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(8): Show |
31 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
34 | HG00423.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(19): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(9): Show |
10 | a0001c0001t0002g0146 a0001c0001t0017g0137 a0001c0002t0005g0083 others(7): Show |
10 | HG00642.hp1 HG01257.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.3701-3011_3701-301 others(20): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | GTTTTTTT others(10): Show |
1 | a0005c0005t0002g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3701-3011_3701-301 others(21): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99907693 | ||||||
chr1:99907693 | G | T | 2 | a0001c0014t0016g0133 a0001c0014t0016g0165 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3701-3019G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907693 | |||||||
chr1:99907702 | G | T | 1 | a0001c0014t0016g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3701-3010G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907702 | |||||||
chr1:99907840 | T | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3701-2872T>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907840 | |||||||
chr1:99907939 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3701-2773T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99907939 | |||||||
chr1:99908045 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.3701-2667G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908045 | |||||||
chr1:99908169 | A | C | 1 | a0001c0001t0002g0145 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3701-2543A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908169 | |||||||
chr1:99908174 | G | A | 32 | a0001c0031t0006g0244 a0003c0015t0012g0195 a0003c0015t0012g0197 others(29): Show |
33 | HG00140.hp1 HG00597.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.3701-2538G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908174 | |||||||
chr1:99908210 | A | AT | 7 | a0007c0009t0004g0054 a0007c0009t0004g0071 a0007c0009t0004g0090 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3701-2490dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99908210 | ||||||
chr1:99908210 | AT | A | 137 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(134): Show |
150 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.3701-2490delT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99908210 | ||||||
chr1:99908231 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-2481A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908231 | |||||||
chr1:99908437 | A | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG01346.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.3701-2275A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908437 | |||||||
chr1:99908534 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-2178A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908534 | |||||||
chr1:99908885 | G | A | 12 | a0001c0002t0006g0042 a0002c0003t0006g0064 a0002c0003t0006g0065 others(9): Show |
13 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.3701-1827G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908885 | |||||||
chr1:99908908 | G | A | 163 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(160): Show |
176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3701-1804G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99908908 | |||||||
chr1:99909127 | C | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0034 |
3 | HG00738.hp2 HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3701-1585C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909127 | |||||||
chr1:99909229 | ACAT | A | 12 | a0001c0002t0006g0042 a0002c0003t0006g0064 a0002c0003t0006g0065 others(9): Show |
13 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.3701-1479_3701-147 others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99909229 | ||||||
chr1:99909306 | T | C | 9 | a0003c0006t0001g0175 a0003c0006t0001g0179 a0003c0006t0001g0180 others(6): Show |
9 | HG00673.hp1 HG00733.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.3701-1406T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909306 | |||||||
chr1:99909374 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.3701-1338G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909374 | |||||||
chr1:99909462 | A | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3701-1250A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909462 | |||||||
chr1:99909486 | G | A | 1 | a0001c0001t0007g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3701-1226G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909486 | |||||||
chr1:99909490 | G | A | 1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3701-1222G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909490 | |||||||
chr1:99909555 | A | G | 13 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0278 others(10): Show |
14 | HG00438.hp1 NA18949.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.3701-1157A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909555 | |||||||
chr1:99909653 | T | A | 171 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(168): Show |
185 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3701-1059T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909653 | |||||||
chr1:99909672 | C | A | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(106): Show |
120 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.3701-1040C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909672 | |||||||
chr1:99909791 | A | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(106): Show |
120 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.3701-921A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909791 | |||||||
chr1:99909799 | TAAGAG | T | 7 | a0007c0009t0004g0054 a0007c0009t0004g0071 a0007c0009t0004g0090 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3701-911_3701-907d others(7): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 99909799 | ||||||
chr1:99909851 | A | G | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.3701-861A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99909851 | |||||||
chr1:99910024 | A | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(96): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.3701-688A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910024 | |||||||
chr1:99910243 | A | G | 3 | a0005c0005t0002g0112 a0005c0005t0002g0115 a0005c0005t0002g0171 |
3 | HG02155.hp2 HG02523.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.3701-469A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910243 | |||||||
chr1:99910318 | A | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-394A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910318 | |||||||
chr1:99910319 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-393C>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910319 | |||||||
chr1:99910501 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-211T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910501 | |||||||
chr1:99910553 | G | A | 2 | a0003c0006t0006g0191 a0003c0006t0006g0192 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3701-159G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910553 | |||||||
chr1:99910635 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3701-77G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910635 | |||||||
chr1:99910647 | A | C | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3701-65A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 27/33 | chr1 | 99910647 | |||||||
chr1:99910892 | G | A | 131 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(128): Show |
143 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.3836+45G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99910892 | |||||||
chr1:99910900 | T | A | 131 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(128): Show |
143 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.3836+53T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99910900 | |||||||
chr1:99911131 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3836+284G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99911131 | |||||||
chr1:99911387 | AAT | A | 29 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(26): Show |
30 | HG00140.hp1 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3836+541_3836+542d others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99911387 | |||||||
chr1:99911425 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
9 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3836+578G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99911425 | |||||||
chr1:99911563 | C | T | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3836+716C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99911563 | |||||||
chr1:99911887 | A | G | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3837-518A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99911887 | |||||||
chr1:99912107 | C | T | 3 | a0001c0001t0003g0230 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG02683.hp2 HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3837-298C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99912107 | |||||||
chr1:99912188 | T | C | 19 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(16): Show |
20 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.3837-217T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99912188 | |||||||
chr1:99912233 | C | T | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.3837-172C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 28/33 | chr1 | 99912233 | |||||||
chr1:99912566 | A | G | 1 | a0001c0001t0017g0136 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3949+49A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912566 | |||||||
chr1:99912579 | G | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3949+62G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912579 | |||||||
chr1:99912584 | C | T | 1 | a0014c0019t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3949+67C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912584 | |||||||
chr1:99912653 | A | C | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3949+136A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912653 | |||||||
chr1:99912811 | A | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.3949+294A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912811 | |||||||
chr1:99912814 | T | C | 1 | a0005c0005t0002g0171 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3949+297T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912814 | |||||||
chr1:99912826 | A | G | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3949+309A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99912826 | |||||||
chr1:99913048 | C | T | 9 | a0001c0001t0007g0208 a0001c0001t0007g0229 a0001c0001t0007g0238 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3950-479C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913048 | |||||||
chr1:99913095 | T | C | 171 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(168): Show |
185 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3950-432T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913095 | |||||||
chr1:99913195 | G | T | 1 | a0001c0002t0001g0034 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3950-332G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913195 | |||||||
chr1:99913289 | A | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3950-238A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913289 | |||||||
chr1:99913361 | T | C | 1 | a0002c0003t0005g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3950-166T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913361 | |||||||
chr1:99913448 | A | T | 1 | a0017c0030t0006g0272 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3950-79A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 29/33 | chr1 | 99913448 | |||||||
chr1:99913913 | C | T | 1 | a0004c0004t0003g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4161+175C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99913913 | |||||||
chr1:99914001 | G | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0034 |
3 | HG00738.hp2 HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.4161+263G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914001 | |||||||
chr1:99914045 | G | A | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4161+307G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914045 | |||||||
chr1:99914130 | G | A | 203 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0210 others(200): Show |
220 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.4161+392G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914130 | |||||||
chr1:99914262 | A | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0120 a0001c0001t0003g0225 others(6): Show |
10 | HG00597.hp1 HG02683.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.4161+524A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914262 | |||||||
chr1:99914288 | C | G | 1 | a0018c0027t0013g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4161+550C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914288 | |||||||
chr1:99914386 | G | A | 2 | a0001c0001t0003g0129 a0003c0006t0001g0190 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4161+648G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914386 | |||||||
chr1:99914410 | T | C | 4 | a0009c0010t0010g0205 a0009c0010t0010g0206 a0009c0010t0010g0207 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4161+672T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914410 | |||||||
chr1:99914481 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.4161+743A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914481 | |||||||
chr1:99914503 | G | A | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4161+765G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914503 | |||||||
chr1:99914626 | A | G | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4162-763A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914626 | |||||||
chr1:99914695 | T | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(96): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.4162-694T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914695 | |||||||
chr1:99914707 | C | T | 1 | a0023c0026t0009g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4162-682C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914707 | |||||||
chr1:99914719 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4162-670A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914719 | |||||||
chr1:99914921 | T | A | 1 | a0004c0004t0004g0253 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4162-468T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99914921 | |||||||
chr1:99915037 | G | A | 2 | a0006c0008t0008g0018 a0006c0008t0008g0201 |
3 | HG02109.hp2 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4162-352G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99915037 | |||||||
chr1:99915065 | T | C | 163 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(160): Show |
176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.4162-324T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99915065 | |||||||
chr1:99915266 | T | A | 1 | a0003c0006t0008g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4162-123T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99915266 | |||||||
chr1:99915300 | T | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4162-89T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99915300 | |||||||
chr1:99915378 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4162-11G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 30/33 | chr1 | 99915378 | |||||||
chr1:99915517 | A | T | 1 | a0001c0001t0003g0135 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4259+31A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99915517 | |||||||
chr1:99915553 | A | AT | 118 | a0001c0001t0001g0213 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
130 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.4259+80dupT | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 99915553 | ||||||
chr1:99915611 | TA | T | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4259+135delA | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 99915611 | ||||||
chr1:99915748 | T | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(96): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.4259+262T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99915748 | |||||||
chr1:99915759 | A | C | 1 | a0005c0005t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4259+273A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99915759 | |||||||
chr1:99915773 | A | AAC | 4 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.4259+302_4259+303d others(4): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 99915773 | ||||||
chr1:99915790 | G | A | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4259+304G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99915790 | |||||||
chr1:99915964 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4260-446A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99915964 | |||||||
chr1:99916022 | A | G | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4260-388A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99916022 | |||||||
chr1:99916031 | A | G | 6 | a0001c0001t0009g0106 a0001c0001t0009g0107 a0001c0001t0011g0114 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4260-379A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99916031 | |||||||
chr1:99916259 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4260-151G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99916259 | |||||||
chr1:99916259 | G | T | 19 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(16): Show |
20 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.4260-151G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99916259 | |||||||
chr1:99916313 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.4260-97G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 31/33 | chr1 | 99916313 | |||||||
chr1:99916529 | T | A | 1 | a0001c0002t0001g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4347+32T>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 32/33 | chr1 | 99916529 | |||||||
chr1:99916825 | A | G | 1 | a0001c0002t0008g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4481+94A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99916825 | |||||||
chr1:99916973 | T | C | 1 | a0002c0003t0005g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4481+242T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99916973 | |||||||
chr1:99916976 | G | C | 17 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0248 others(14): Show |
18 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.4481+245G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99916976 | |||||||
chr1:99917190 | C | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4481+459C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917190 | |||||||
chr1:99917383 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4481+652C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917383 | |||||||
chr1:99917446 | A | T | 1 | a0002c0003t0005g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4481+715A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917446 | |||||||
chr1:99917449 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.4481+718T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917449 | |||||||
chr1:99917461 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
114 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.4481+730A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917461 | |||||||
chr1:99917495 | G | A | 1 | a0005c0005t0002g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4481+764G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917495 | |||||||
chr1:99917507 | G | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.4481+776G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917507 | |||||||
chr1:99917840 | A | C | 1 | a0003c0006t0001g0180 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4481+1109A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917840 | |||||||
chr1:99917907 | A | G | 1 | a0004c0004t0004g0262 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4481+1176A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99917907 | |||||||
chr1:99918057 | A | G | 6 | a0002c0003t0006g0067 a0002c0003t0006g0068 a0002c0003t0006g0094 others(3): Show |
7 | NA18953.hp1 NA18967.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.4481+1326A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918057 | |||||||
chr1:99918209 | C | T | 1 | a0004c0004t0004g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.4481+1478C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918209 | |||||||
chr1:99918358 | G | C | 1 | a0005c0005t0002g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4481+1627G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918358 | |||||||
chr1:99918364 | G | A | 1 | a0005c0005t0002g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4481+1633G>A | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918364 | |||||||
chr1:99918532 | C | T | 1 | a0001c0031t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4481+1801C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918532 | |||||||
chr1:99918661 | A | T | 3 | a0010c0011t0014g0202 a0010c0011t0014g0245 a0024c0016t0023g0203 |
3 | HG01167.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4481+1930A>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918661 | |||||||
chr1:99918717 | G | C | 1 | a0005c0005t0002g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4481+1986G>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918717 | |||||||
chr1:99918806 | G | T | 1 | a0008c0013t0004g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4481+2075G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918806 | |||||||
chr1:99918846 | A | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(101): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.4481+2115A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918846 | |||||||
chr1:99918861 | C | G | 1 | a0006c0008t0008g0018 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4481+2130C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918861 | |||||||
chr1:99918895 | GGCTGGTG others(22): Show |
G | 2 | a0003c0015t0012g0195 a0003c0015t0012g0197 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4481+2169_4481+219 others(33): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 99918895 | ||||||
chr1:99918988 | G | T | 29 | a0004c0004t0004g0015 a0004c0004t0004g0016 a0004c0004t0004g0017 others(26): Show |
30 | HG00140.hp1 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4481+2257G>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99918988 | |||||||
chr1:99919418 | A | G | 1 | a0001c0002t0008g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4482-2116A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99919418 | |||||||
chr1:99919538 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4482-1996A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99919538 | |||||||
chr1:99919753 | T | C | 101 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(98): Show |
112 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.4482-1781T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99919753 | |||||||
chr1:99919874 | C | T | 19 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0002c0003t0006g0064 others(16): Show |
20 | HG00733.hp2 HG01069.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.4482-1660C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99919874 | |||||||
chr1:99919932 | A | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0142 |
3 | HG03654.hp2 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4482-1602A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99919932 | |||||||
chr1:99920205 | T | C | 2 | a0004c0004t0004g0253 a0004c0004t0004g0255 |
2 | HG02559.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.4482-1329T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99920205 | |||||||
chr1:99920471 | C | G | 1 | a0001c0002t0001g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4482-1063C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99920471 | |||||||
chr1:99921126 | C | T | 1 | a0002c0003t0006g0094 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4482-408C>T | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99921126 | |||||||
chr1:99921155 | ATTACTT | A | 23 | a0001c0001t0006g0204 a0001c0002t0006g0042 a0001c0031t0006g0244 others(20): Show |
24 | HG00733.hp2 HG01069.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4482-368_4482-363d others(8): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 99921155 | ||||||
chr1:99921180 | C | CAGAT | 3 | a0001c0001t0006g0204 a0003c0006t0006g0191 a0003c0006t0006g0192 |
3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4482-353_4482-352i others(6): Show |
AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 99921180 | ||||||
chr1:99921200 | C | G | 1 | a0001c0002t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4482-334C>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99921200 | |||||||
chr1:99921260 | A | G | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG01346.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.4482-274A>G | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99921260 | |||||||
chr1:99921305 | T | C | 1 | a0003c0006t0019g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4482-229T>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99921305 | |||||||
chr1:99921430 | A | C | 1 | a0001c0001t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4482-104A>C | AGL | ENSG00000162688.17 | transcript | ENST00000361915.8 | protein_coding | 33/33 | chr1 | 99921430 |