Item | Value |
---|---|
geneid | 22877 |
ensemblid | ENSG00000175727.15 |
hgncid | 17055 |
symbol | MLXIP |
name | MLX interacting protein |
refseq_nuc | NM_014938.6 |
refseq_prot | NP_055753.3 |
ensembl_nuc | ENST00000319080.12 |
ensembl_prot | ENSP00000312834.6 |
mane_status | MANE Select |
chr | chr12 |
start | 122078756 |
end | 122147344 |
strand | + |
ver | v1.2 |
region | chr12:122078756-122147344 |
region5000 | chr12:122073756-122152344 |
regionname0 | MLXIP_chr12_122078756_122147344 |
regionname5000 | MLXIP_chr12_122073756_122152344 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 919 | 184 | 25 | 50 | 73 | 9 | 26 | 55 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0002 | 0/1 | 919 | 145 | 42 | 21 | 60 | 5 | 16 | 43 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0003 | 0/0 | 919 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0004 | 0/0 | 919 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0005 | 0/0 | 919 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0006 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0007 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0008 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0009 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0010 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0011 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0012 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0013 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
a0014 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(909): Show |
chr12 | 122073756 | 122152344 |
a0015 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | MAADV others(914): Show |
chr12 | 122073756 | 122152344 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2757 | 136 | 20 | 34 | 52 | 5 | 24 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0001c0003 | 0/0 | 2757 | 43 | 2 | 16 | 20 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0001c0008 | 0/0 | 2757 | 4 | 3 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0001c0019 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0002 | 0/0 | 2757 | 78 | 18 | 12 | 39 | 1 | 8 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0004 | 0/0 | 2757 | 41 | 15 | 3 | 17 | 0 | 6 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0005 | 0/1 | 2757 | 12 | 0 | 6 | 0 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0009 | 0/0 | 2757 | 4 | 2 | 0 | 1 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0010 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0011 | 0/0 | 2757 | 3 | 0 | 0 | 3 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0024 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0026 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0002c0027 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0003c0006 | 0/0 | 2757 | 7 | 7 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0003c0018 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0004c0007 | 0/0 | 2757 | 5 | 4 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0005c0012 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0006c0013 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0007c0023 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0008c0017 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0009c0020 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0010c0021 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0011c0014 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0012c0016 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0013c0025 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 | ||
a0014c0022 | 0/0 | 2742 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2737): Show |
chr12 | 122073756 | 122152344 | ||
a0015c0015 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | ATGGC others(2752): Show |
chr12 | 122073756 | 122152344 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8388 | 62 | 6 | 14 | 23 | 4 | 15 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0006 | 0/0 | 8388 | 11 | 0 | 1 | 10 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0007 | 0/0 | 8389 | 8 | 0 | 1 | 6 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0008 | 0/0 | 8388 | 8 | 0 | 7 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0011 | 0/0 | 8388 | 5 | 4 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0013 | 0/0 | 8390 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0014 | 0/0 | 8389 | 5 | 0 | 1 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0015 | 0/0 | 8387 | 4 | 0 | 2 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0018 | 0/0 | 8390 | 4 | 0 | 3 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0022 | 0/0 | 8386 | 3 | 0 | 0 | 0 | 0 | 3 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8381): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0029 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0030 | 0/0 | 8388 | 2 | 0 | 2 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0031 | 0/0 | 8388 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0032 | 0/0 | 8388 | 2 | 0 | 0 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0033 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0035 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0042 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0043 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0057 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0058 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0059 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0061 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0062 | 1/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0063 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0064 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0001c0001t0070 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0003 | 0/0 | 8388 | 35 | 1 | 15 | 15 | 3 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0004 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0007 | 0/0 | 8389 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0020 | 0/0 | 8389 | 2 | 1 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0025 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0046 | 0/0 | 8389 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0049 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0003t0051 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0008t0028 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0001c0008t0047 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0001c0008t0055 | 0/0 | 8384 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8379): Show |
chr12 | 122073756 | 122152344 |
a0001c0019t0001 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0002 | 0/0 | 8380 | 47 | 4 | 9 | 28 | 1 | 5 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0005 | 0/0 | 8368 | 3 | 3 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8363): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0010 | 0/0 | 8389 | 6 | 0 | 0 | 6 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0012 | 0/0 | 8384 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8379): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0016 | 0/0 | 8380 | 3 | 0 | 2 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0021 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0023 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0026 | 0/0 | 8380 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0027 | 0/0 | 8391 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8386): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0037 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0038 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0039 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0040 | 0/0 | 8380 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0041 | 0/0 | 8389 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0044 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0054 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0002t0071 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0003 | 0/0 | 8388 | 8 | 4 | 0 | 0 | 0 | 4 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0004 | 0/0 | 8388 | 9 | 0 | 0 | 9 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0005 | 0/0 | 8368 | 11 | 5 | 2 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8363): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0020 | 0/0 | 8389 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0021 | 0/0 | 8388 | 2 | 1 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0024 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0048 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0052 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0053 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0056 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0065 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8363): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0066 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8363): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0067 | 0/0 | 8368 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8363): Show |
chr12 | 122073756 | 122152344 |
a0002c0004t0068 | 0/0 | 8367 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8362): Show |
chr12 | 122073756 | 122152344 |
a0002c0005t0004 | 0/0 | 8388 | 4 | 0 | 2 | 0 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0005t0009 | 0/1 | 8388 | 6 | 0 | 3 | 0 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0005t0045 | 0/0 | 8389 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8384): Show |
chr12 | 122073756 | 122152344 |
a0002c0005t0050 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0009t0001 | 0/0 | 8388 | 2 | 0 | 0 | 1 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0009t0011 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0009t0069 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0010t0017 | 0/0 | 8380 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0011t0002 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0011t0016 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0011t0036 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0002c0024t0002 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0002c0026t0003 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0002c0027t0003 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0003c0006t0001 | 0/0 | 8388 | 6 | 6 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0003c0006t0015 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0003c0018t0060 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0004c0007t0019 | 0/0 | 8385 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8380): Show |
chr12 | 122073756 | 122152344 |
a0004c0007t0034 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0004c0007t0074 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0004c0007t0075 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0005c0012t0072 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0005c0012t0073 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8385): Show |
chr12 | 122073756 | 122152344 |
a0006c0013t0002 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0007c0023t0002 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8375): Show |
chr12 | 122073756 | 122152344 |
a0008c0017t0001 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0009c0020t0019 | 0/0 | 8385 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8380): Show |
chr12 | 122073756 | 122152344 |
a0010c0021t0076 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8373): Show |
chr12 | 122073756 | 122152344 |
a0011c0014t0019 | 0/0 | 8385 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8380): Show |
chr12 | 122073756 | 122152344 |
a0012c0016t0003 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
a0013c0025t0025 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8382): Show |
chr12 | 122073756 | 122152344 |
a0014c0022t0023 | 0/0 | 8365 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8360): Show |
chr12 | 122073756 | 122152344 |
a0015c0015t0003 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | AGTCG others(8383): Show |
chr12 | 122073756 | 122152344 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0007g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0011g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0013g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0014g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0014g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0015g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0015g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0015g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0018g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0018g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0018g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0022g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0022g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0022g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0029g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0030g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0030g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0031g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0031g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0032g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0032g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0033g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0033g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0035g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0042g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0043g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0057g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0058g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0059g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0061g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0062g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0063g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0064g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0001t0070g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0020g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0020g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0025g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0046g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0049g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0003t0051g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0008t0028g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0008t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0008t0047g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0008t0055g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0001c0019t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0012g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0016g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0016g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0021g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0023g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0026g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0027g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0037g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0038g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0039g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0040g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0041g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0044g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0054g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0002t0071g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0020g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0021g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0048g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0052g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0053g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0056g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0065g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0066g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0067g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0004t0068g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0045g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0005t0050g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0009t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0009t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0009t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0009t0069g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0010t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0010t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0010t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0010t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0011t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0011t0016g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0011t0036g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0024t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0026t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0002c0027t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0006t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0003c0018t0060g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0004c0007t0019g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0004c0007t0034g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0004c0007t0034g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0004c0007t0074g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0004c0007t0075g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0005c0012t0072g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0005c0012t0073g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0006c0013t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0007c0023t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0008c0017t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0009c0020t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0010c0021t0076g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0011c0014t0019g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0012c0016t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0013c0025t0025g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0014c0022t0023g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
a0015c0015t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0003 | g0310 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00140 | hp1 | a0001 | c0001 | t0018 | g0104 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00280 | hp2 | a0001 | c0003 | t0003 | g0317 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00323 | hp1 | a0002 | c0005 | t0009 | g0240 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0340 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00544 | hp1 | a0002 | c0002 | t0037 | g0219 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00558 | hp2 | a0002 | c0011 | t0016 | g0005 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00597 | hp2 | a0001 | c0008 | t0047 | g0289 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00621 | hp1 | a0001 | c0001 | t0035 | g0100 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00621 | hp2 | a0002 | c0002 | t0071 | g0021 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0298 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0167 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00741 | hp1 | a0001 | c0001 | t0018 | g0082 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG00741 | hp2 | a0001 | c0003 | t0003 | g0314 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01069 | hp1 | a0002 | c0005 | t0004 | g0237 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0165 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01070 | hp1 | a0001 | c0003 | t0003 | g0306 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01071 | hp1 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01074 | hp1 | a0001 | c0003 | t0049 | g0308 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0070 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01099 | hp1 | a0002 | c0005 | t0009 | g0241 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01099 | hp2 | a0004 | c0007 | t0019 | g0335 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0105 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0118 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01109 | hp1 | a0002 | c0005 | t0009 | g0236 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01109 | hp2 | a0006 | c0013 | t0002 | g0229 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01168 | hp1 | a0001 | c0001 | t0030 | g0059 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01169 | hp2 | a0001 | c0001 | t0030 | g0058 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01175 | hp1 | a0002 | c0005 | t0045 | g0232 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01175 | hp2 | a0001 | c0001 | t0018 | g0083 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01192 | hp2 | a0001 | c0001 | t0061 | g0103 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0052 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01243 | hp2 | a0002 | c0004 | t0067 | g0173 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01257 | hp1 | a0001 | c0001 | t0014 | g0140 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01257 | hp2 | a0001 | c0001 | t0015 | g0175 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01261 | hp2 | a0002 | c0002 | t0038 | g0230 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0276 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01361 | hp1 | a0002 | c0005 | t0004 | g0234 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01361 | hp2 | a0001 | c0003 | t0003 | g0303 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01433 | hp1 | a0001 | c0003 | t0003 | g0304 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01433 | hp2 | a0002 | c0002 | t0016 | g0186 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0319 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01496 | hp2 | a0002 | c0002 | t0016 | g0177 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01515 | hp1 | a0002 | c0005 | t0050 | g0238 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01515 | hp2 | a0001 | c0019 | t0001 | g0117 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01516 | hp1 | a0002 | c0005 | t0004 | g0275 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01516 | hp2 | a0002 | c0009 | t0001 | g0280 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01884 | hp1 | a0002 | c0002 | t0012 | g0210 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01884 | hp2 | a0004 | c0007 | t0034 | g0332 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01891 | hp1 | a0002 | c0010 | t0017 | g0170 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01891 | hp2 | a0002 | c0002 | t0021 | g0181 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01934 | hp1 | a0002 | c0005 | t0009 | g0239 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0312 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01943 | hp2 | a0001 | c0001 | t0015 | g0145 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01952 | hp1 | a0001 | c0001 | t0006 | g0126 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0307 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01975 | hp1 | a0001 | c0001 | t0008 | g0081 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01978 | hp1 | a0001 | c0003 | t0003 | g0318 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0324 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01981 | hp2 | a0007 | c0023 | t0002 | g0341 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01993 | hp1 | a0002 | c0004 | t0005 | g0008 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02004 | hp1 | a0001 | c0003 | t0003 | g0320 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02004 | hp2 | a0001 | c0001 | t0018 | g0106 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02015 | hp2 | a0001 | c0003 | t0025 | g0297 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02027 | hp2 | a0002 | c0002 | t0010 | g0019 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02040 | hp2 | a0008 | c0017 | t0001 | g0110 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02055 | hp1 | a0001 | c0001 | t0029 | g0053 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02055 | hp2 | a0002 | c0009 | t0069 | g0035 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02080 | hp2 | a0002 | c0011 | t0036 | g0264 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02083 | hp1 | a0002 | c0004 | t0004 | g0274 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02083 | hp2 | a0001 | c0001 | t0031 | g0338 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02129 | hp1 | a0001 | c0003 | t0003 | g0316 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02129 | hp2 | a0002 | c0004 | t0005 | g0007 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0284 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02135 | hp2 | a0002 | c0009 | t0001 | g0057 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02145 | hp1 | a0001 | c0001 | t0033 | g0164 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02145 | hp2 | a0002 | c0004 | t0005 | g0168 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02148 | hp1 | a0001 | c0003 | t0003 | g0302 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02148 | hp2 | a0001 | c0001 | t0070 | g0101 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0109 | EAS | CDX | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02155 | hp2 | a0002 | c0002 | t0023 | g0260 | EAS | CDX | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02257 | hp1 | a0002 | c0004 | t0003 | g0193 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02257 | hp2 | a0003 | c0006 | t0001 | g0030 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02258 | hp1 | a0002 | c0004 | t0020 | g0194 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02258 | hp2 | a0002 | c0002 | t0012 | g0004 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02273 | hp1 | a0001 | c0003 | t0003 | g0323 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02273 | hp2 | a0001 | c0003 | t0003 | g0309 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02280 | hp1 | a0002 | c0002 | t0012 | g0212 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02280 | hp2 | a0002 | c0002 | t0026 | g0187 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02300 | hp1 | a0002 | c0004 | t0005 | g0013 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02451 | hp1 | a0001 | c0001 | t0057 | g0344 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02615 | hp1 | a0002 | c0010 | t0017 | g0172 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0326 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02622 | hp2 | a0002 | c0027 | t0003 | g0040 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02630 | hp2 | a0009 | c0020 | t0019 | g0337 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02647 | hp1 | a0002 | c0024 | t0002 | g0328 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02647 | hp2 | a0002 | c0010 | t0017 | g0169 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0267 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02717 | hp1 | a0004 | c0007 | t0075 | g0333 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02717 | hp2 | a0003 | c0018 | t0060 | g0179 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0038 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02723 | hp2 | a0003 | c0006 | t0001 | g0029 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02735 | hp1 | a0002 | c0002 | t0016 | g0269 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0342 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02738 | hp1 | a0002 | c0005 | t0009 | g0233 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02809 | hp1 | a0002 | c0004 | t0005 | g0048 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02809 | hp2 | a0002 | c0002 | t0026 | g0202 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02895 | hp1 | a0005 | c0012 | t0073 | g0159 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02895 | hp2 | a0002 | c0002 | t0027 | g0015 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02896 | hp1 | a0002 | c0002 | t0005 | g0041 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02896 | hp2 | a0001 | c0008 | t0055 | g0215 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02897 | hp1 | a0002 | c0002 | t0005 | g0043 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02897 | hp2 | a0002 | c0002 | t0027 | g0014 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02922 | hp1 | a0004 | c0007 | t0034 | g0331 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02922 | hp2 | a0005 | c0012 | t0072 | g0160 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02965 | hp1 | a0003 | c0006 | t0015 | g0067 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02976 | hp2 | a0002 | c0004 | t0003 | g0242 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0220 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03041 | hp2 | a0003 | c0006 | t0001 | g0033 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03139 | hp1 | a0003 | c0006 | t0001 | g0031 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03195 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0056 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03209 | hp1 | a0002 | c0002 | t0012 | g0211 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03209 | hp2 | a0002 | c0004 | t0003 | g0204 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03225 | hp2 | a0003 | c0006 | t0001 | g0032 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0272 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03453 | hp1 | a0002 | c0009 | t0011 | g0055 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03486 | hp1 | a0002 | c0004 | t0065 | g0047 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03486 | hp2 | a0002 | c0026 | t0003 | g0201 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0227 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03490 | hp2 | a0001 | c0001 | t0022 | g0076 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03491 | hp1 | a0001 | c0001 | t0015 | g0143 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03491 | hp2 | a0002 | c0005 | t0004 | g0231 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0327 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03516 | hp2 | a0003 | c0006 | t0001 | g0034 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03540 | hp1 | a0002 | c0004 | t0024 | g0184 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03540 | hp2 | a0002 | c0002 | t0012 | g0004 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03579 | hp1 | a0010 | c0021 | t0076 | g0012 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0329 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03669 | hp2 | a0002 | c0004 | t0048 | g0196 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03688 | hp1 | a0002 | c0004 | t0003 | g0217 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03688 | hp2 | a0002 | c0002 | t0040 | g0262 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03704 | hp1 | a0002 | c0002 | t0041 | g0020 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03710 | hp2 | a0001 | c0001 | t0022 | g0090 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03831 | hp1 | a0001 | c0001 | t0022 | g0161 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0148 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03834 | hp1 | a0002 | c0004 | t0005 | g0009 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03927 | hp1 | a0001 | c0003 | t0051 | g0288 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0305 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03942 | hp1 | a0001 | c0001 | t0032 | g0093 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03942 | hp2 | a0001 | c0001 | t0058 | g0066 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04184 | hp2 | a0001 | c0001 | t0014 | g0069 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04199 | hp2 | a0002 | c0004 | t0003 | g0183 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04204 | hp1 | a0002 | c0004 | t0003 | g0176 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04228 | hp1 | a0002 | c0004 | t0003 | g0216 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0259 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18522 | hp2 | a0001 | c0001 | t0033 | g0163 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18612 | hp1 | a0002 | c0002 | t0010 | g0024 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18612 | hp2 | a0002 | c0004 | t0005 | g0010 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18747 | hp1 | a0001 | c0001 | t0031 | g0339 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18747 | hp2 | a0002 | c0002 | t0010 | g0026 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18939 | hp2 | a0001 | c0003 | t0003 | g0325 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18941 | hp1 | a0002 | c0002 | t0010 | g0022 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18941 | hp2 | a0001 | c0001 | t0032 | g0111 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18942 | hp2 | a0002 | c0004 | t0004 | g0207 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18943 | hp1 | a0002 | c0002 | t0039 | g0228 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18944 | hp2 | a0001 | c0003 | t0004 | g0287 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18948 | hp1 | a0001 | c0003 | t0003 | g0282 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18950 | hp1 | a0001 | c0003 | t0003 | g0322 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18950 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18951 | hp2 | a0001 | c0001 | t0059 | g0072 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18953 | hp2 | a0002 | c0004 | t0053 | g0190 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18956 | hp1 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18961 | hp1 | a0012 | c0016 | t0003 | g0285 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18964 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18964 | hp2 | a0001 | c0001 | t0014 | g0134 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18967 | hp1 | a0002 | c0004 | t0052 | g0213 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18967 | hp2 | a0001 | c0001 | t0014 | g0153 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18968 | hp1 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18969 | hp2 | a0002 | c0004 | t0005 | g0017 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18971 | hp2 | a0001 | c0003 | t0003 | g0293 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18972 | hp1 | a0002 | c0004 | t0004 | g0206 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18973 | hp2 | a0002 | c0004 | t0004 | g0208 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18974 | hp2 | a0013 | c0025 | t0025 | g0294 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18979 | hp1 | a0002 | c0004 | t0004 | g0195 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18981 | hp2 | a0002 | c0002 | t0054 | g0300 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18982 | hp2 | a0001 | c0001 | t0043 | g0050 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18983 | hp1 | a0002 | c0011 | t0002 | g0257 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18988 | hp1 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18989 | hp1 | a0002 | c0004 | t0004 | g0209 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18991 | hp2 | a0002 | c0004 | t0004 | g0189 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18993 | hp1 | a0001 | c0001 | t0042 | g0049 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18993 | hp2 | a0001 | c0003 | t0020 | g0321 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18994 | hp1 | a0002 | c0004 | t0004 | g0214 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18994 | hp2 | a0001 | c0003 | t0007 | g0068 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19001 | hp1 | a0001 | c0001 | t0015 | g0123 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19004 | hp1 | a0001 | c0001 | t0006 | g0330 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19004 | hp2 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19005 | hp2 | a0001 | c0003 | t0003 | g0292 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19007 | hp1 | a0002 | c0002 | t0010 | g0025 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19009 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19012 | hp1 | a0001 | c0001 | t0063 | g0146 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19043 | hp1 | a0002 | c0010 | t0017 | g0171 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19043 | hp2 | a0001 | c0003 | t0003 | g0301 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19054 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19060 | hp1 | a0001 | c0001 | t0007 | g0281 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19060 | hp2 | a0014 | c0022 | t0023 | g0261 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19062 | hp1 | a0001 | c0001 | t0064 | g0097 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19062 | hp2 | a0002 | c0002 | t0010 | g0023 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19066 | hp1 | a0002 | c0004 | t0066 | g0011 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19066 | hp2 | a0002 | c0004 | t0021 | g0180 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19067 | hp1 | a0002 | c0004 | t0004 | g0205 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19068 | hp2 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0311 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19083 | hp2 | a0002 | c0004 | t0056 | g0218 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19085 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19086 | hp1 | a0015 | c0015 | t0003 | g0098 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0346 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19087 | hp1 | a0001 | c0003 | t0046 | g0296 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19240 | hp1 | a0002 | c0004 | t0005 | g0045 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA19240 | hp2 | a0002 | c0002 | t0005 | g0027 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0279 | AFR | ASW | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20129 | hp2 | a0001 | c0008 | t0028 | g0018 | AFR | ASW | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20752 | hp1 | a0001 | c0003 | t0003 | g0313 | EUR | TSI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01123 | hp1 | a0001 | c0003 | t0003 | g0315 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02109 | hp1 | a0002 | c0002 | t0044 | g0203 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02109 | hp2 | a0002 | c0004 | t0005 | g0044 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0345 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0064 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02559 | hp1 | a0001 | c0001 | t0029 | g0343 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG02559 | hp2 | a0004 | c0007 | t0074 | g0334 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03471 | hp1 | a0002 | c0004 | t0003 | g0192 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG03471 | hp2 | a0001 | c0008 | t0028 | g0016 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG06807 | hp1 | a0011 | c0014 | t0019 | g0336 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
HG06807 | hp2 | a0002 | c0004 | t0068 | g0042 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA18955 | hp2 | a0001 | c0001 | t0014 | g0096 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20300 | hp1 | a0001 | c0003 | t0020 | g0006 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA20300 | hp2 | a0002 | c0004 | t0024 | g0185 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA21309 | hp1 | a0002 | c0004 | t0021 | g0182 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
NA21309 | hp2 | a0002 | c0004 | t0005 | g0046 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
homoSapiens | chm13v2 | a0002 | c0005 | t0009 | g0235 | REF | REF | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
homoSapiens | grch38p0 | a0001 | c0001 | t0062 | g0191 | REF | REF | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:122078986 | G | A | 1 | a0006 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.133G>A | p.Gly45Ser | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 231/8390 | 133/2760 | 45/919 | chr12 | 122078986 | |||
chr12:122127352 | G | T | 1 | a0013 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.510G>T | p.Trp170Cys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/17 | 608/8390 | 510/2760 | 170/919 | chr12 | 122127352 | |||
chr12:122133372 | C | A | 3 | a0004 a0005 a0011 |
8 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.1117C>A | p.Leu373Ile | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1215/8390 | 1117/2760 | 373/919 | chr12 | 122133372 | |||
chr12:122133442 | A | G | 6 | a0002 a0006 a0007 others(3): Show |
149 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(146): Show |
missense_variant | MODERATE | c.1187A>G | p.Glu396Gly | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1285/8390 | 1187/2760 | 396/919 | chr12 | 122133442 | |||
chr12:122133697 | C | T | 4 | a0004 a0005 a0009 others(1): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.1442C>T | p.Pro481Leu | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1540/8390 | 1442/2760 | 481/919 | chr12 | 122133697 | |||
chr12:122133870 | G | T | 1 | a0003 | 8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.1615G>T | p.Val539Leu | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1713/8390 | 1615/2760 | 539/919 | chr12 | 122133870 | |||
chr12:122133915 | C | G | 1 | a0015 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.1660C>G | p.Pro554Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1758/8390 | 1660/2760 | 554/919 | chr12 | 122133915 | |||
chr12:122135301 | G | A | 1 | a0012 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.1810G>A | p.Val604Met | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 10/17 | 1908/8390 | 1810/2760 | 604/919 | chr12 | 122135301 | |||
chr12:122138248 | A | G | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.2209A>G | p.Met737Val | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 13/17 | 2307/8390 | 2209/2760 | 737/919 | chr12 | 122138248 | |||
chr12:122138529 | G | A | 1 | a0008 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2362G>A | p.Glu788Lys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/17 | 2460/8390 | 2362/2760 | 788/919 | chr12 | 122138529 | |||
chr12:122138895 | AATACGTG others(8): Show |
A | 1 | a0014 | 1 | NA19060.hp2 | disruptive_inframe_deletion | MODERATE | c.2466_2480delATACGT others(9): Show |
p.Tyr823_Arg827del | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/17 | 2564/8390 | 2466/2760 | 822/919 | chr12 | 122138895 | |||
chr12:122140961 | T | G | 1 | a0005 | 2 | HG02895.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.2516T>G | p.Ile839Ser | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/17 | 2614/8390 | 2516/2760 | 839/919 | chr12 | 122140961 | |||
chr12:122141784 | G | A | 1 | a0010 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2732G>A | p.Arg911Lys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2830/8390 | 2732/2760 | 911/919 | chr12 | 122141784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:122078886 | C | T | 2 | a0002c0026 a0002c0027 |
2 | HG02622.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.33C>T | p.Arg11Arg | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 131/8390 | 33/2760 | 11/919 | chr12 | 122078886 | |||
chr12:122078895 | C | T | 1 | a0002c0011 | 3 | HG00558.hp2 HG02080.hp2 NA18983.hp1 |
synonymous_variant | LOW | c.42C>T | p.Arg14Arg | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 140/8390 | 42/2760 | 14/919 | chr12 | 122078895 | |||
chr12:122078991 | G | A | 1 | a0002c0005 | 11 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(8): Show |
synonymous_variant | LOW | c.138G>A | p.Ala46Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 236/8390 | 138/2760 | 46/919 | chr12 | 122078991 | |||
chr12:122133584 | A | G | 7 | a0001c0008 a0002c0002 a0002c0011 others(4): Show |
89 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
synonymous_variant | LOW | c.1329A>G | p.Pro443Pro | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1427/8390 | 1329/2760 | 443/919 | chr12 | 122133584 | |||
chr12:122133743 | C | T | 1 | a0002c0010 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.1488C>T | p.Ala496Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1586/8390 | 1488/2760 | 496/919 | chr12 | 122133743 | |||
chr12:122133746 | C | T | 1 | a0001c0019 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1491C>T | p.Pro497Pro | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1589/8390 | 1491/2760 | 497/919 | chr12 | 122133746 | |||
chr12:122133887 | A | G | 1 | a0002c0027 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1632A>G | p.Val544Val | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1730/8390 | 1632/2760 | 544/919 | chr12 | 122133887 | |||
chr12:122133914 | G | A | 1 | a0015c0015 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1659G>A | p.Gln553Gln | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1757/8390 | 1659/2760 | 553/919 | chr12 | 122133914 | |||
chr12:122135327 | G | T | 1 | a0002c0024 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1836G>T | p.Ala612Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 10/17 | 1934/8390 | 1836/2760 | 612/919 | chr12 | 122135327 | |||
chr12:122138453 | T | C | 22 | a0001c0003 a0001c0008 a0002c0002 others(19): Show |
204 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
synonymous_variant | LOW | c.2286T>C | p.Thr762Thr | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/17 | 2384/8390 | 2286/2760 | 762/919 | chr12 | 122138453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:122078765 | GCGGGC | G | 3 | a0004c0007t0019 a0009c0020t0019 a0011c0014t0019 |
3 | HG01099.hp2 HG02630.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75_-71delGCCGG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 71 | INFO_REALIGN_3_PRIME | chr12 | 122078765 | |||||
chr12:122078767 | G | T | 1 | a0002c0002t0002 | 2 | HG02698.hp2 HG03239.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | chr12 | 122078767 | |||||||
chr12:122078770 | C | T | 1 | a0001c0001t0001 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 84 | chr12 | 122078770 | ||||||
chr12:122078773 | G | T | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 81 | chr12 | 122078773 | ||||||
chr12:122078797 | C | T | 8 | a0004c0007t0019 a0004c0007t0034 a0004c0007t0074 others(5): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | chr12 | 122078797 | |||||||
chr12:122078801 | C | T | 1 | a0002c0002t0071 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 53 | chr12 | 122078801 | ||||||
chr12:122078811 | G | A | 1 | a0001c0001t0035 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 43 | chr12 | 122078811 | ||||||
chr12:122141831 | G | A | 1 | a0002c0011t0036 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 19 | chr12 | 122141831 | ||||||
chr12:122141834 | G | A | 14 | a0002c0002t0002 a0002c0002t0016 a0002c0002t0023 others(11): Show |
62 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 22 | chr12 | 122141834 | ||||||
chr12:122141938 | A | G | 1 | a0001c0001t0033 | 2 | HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*126A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 126 | chr12 | 122141938 | ||||||
chr12:122142054 | C | G | 6 | a0004c0007t0019 a0004c0007t0034 a0004c0007t0074 others(3): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 242 | chr12 | 122142054 | ||||||
chr12:122142153 | G | A | 3 | a0001c0001t0042 a0001c0001t0043 a0002c0002t0041 |
3 | HG03704.hp1 NA18982.hp2 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 341 | chr12 | 122142153 | ||||||
chr12:122142153 | G | C | 1 | a0002c0002t0044 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 341 | chr12 | 122142153 | ||||||
chr12:122142159 | G | A | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 347 | chr12 | 122142159 | ||||||
chr12:122142209 | CCCTCCTG others(3): Show |
C | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399_*408delCTCCTG others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 399 | INFO_REALIGN_3_PRIME | chr12 | 122142209 | |||||
chr12:122142262 | C | T | 1 | a0001c0001t0070 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 450 | chr12 | 122142262 | ||||||
chr12:122142295 | G | A | 52 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(49): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 483 | chr12 | 122142295 | ||||||
chr12:122142616 | C | T | 2 | a0001c0008t0028 a0002c0002t0027 |
4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*804C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 804 | chr12 | 122142616 | ||||||
chr12:122142617 | G | A | 1 | a0002c0002t0037 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 805 | chr12 | 122142617 | ||||||
chr12:122142824 | G | A | 26 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(23): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1012G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1012 | chr12 | 122142824 | ||||||
chr12:122142868 | G | C | 4 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0030 others(1): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1056G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1056 | chr12 | 122142868 | ||||||
chr12:122143135 | C | T | 1 | a0002c0010t0017 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1323 | chr12 | 122143135 | ||||||
chr12:122143339 | C | T | 6 | a0001c0008t0028 a0002c0002t0010 a0002c0002t0027 others(3): Show |
13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1527C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1527 | chr12 | 122143339 | ||||||
chr12:122143672 | T | C | 53 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(50): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1860T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1860 | chr12 | 122143672 | ||||||
chr12:122143754 | C | T | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1942 | chr12 | 122143754 | ||||||
chr12:122143760 | G | T | 1 | a0002c0009t0069 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1948G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1948 | chr12 | 122143760 | ||||||
chr12:122143788 | G | C | 2 | a0001c0001t0013 a0001c0001t0057 |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1976G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1976 | chr12 | 122143788 | ||||||
chr12:122143822 | C | G | 1 | a0001c0001t0030 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2010C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2010 | chr12 | 122143822 | ||||||
chr12:122143882 | T | A | 15 | a0002c0002t0002 a0002c0002t0016 a0002c0002t0023 others(12): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2070T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2070 | chr12 | 122143882 | ||||||
chr12:122143918 | G | A | 2 | a0002c0002t0023 a0014c0022t0023 |
2 | HG02155.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2106G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2106 | chr12 | 122143918 | ||||||
chr12:122143969 | A | T | 53 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(50): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2157A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2157 | chr12 | 122143969 | ||||||
chr12:122143990 | C | T | 16 | a0001c0001t0013 a0001c0001t0057 a0002c0002t0005 others(13): Show |
33 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2178C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2178 | chr12 | 122143990 | ||||||
chr12:122144202 | G | T | 2 | a0001c0001t0013 a0001c0001t0057 |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2390G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2390 | chr12 | 122144202 | ||||||
chr12:122144203 | G | T | 2 | a0001c0001t0013 a0001c0001t0057 |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2391G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2391 | chr12 | 122144203 | ||||||
chr12:122144215 | C | T | 1 | a0002c0004t0053 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2403 | chr12 | 122144215 | ||||||
chr12:122144418 | C | CA | 14 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0029 others(11): Show |
35 | HG01106.hp2 HG01175.hp1 HG01257.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2630dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2631 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | |||||
chr12:122144418 | CA | C | 6 | a0001c0001t0015 a0001c0001t0064 a0001c0003t0025 others(3): Show |
9 | HG01257.hp2 HG01943.hp2 HG02015.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2630delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2630 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | |||||
chr12:122144418 | CAAAAAA | C | 2 | a0001c0008t0055 a0002c0002t0012 |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2625_*2630delAAAA others(2): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2625 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | |||||
chr12:122144418 | CAAAAAAA others(3): Show |
C | 17 | a0002c0002t0002 a0002c0002t0016 a0002c0002t0023 others(14): Show |
69 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2621_*2630delAAAA others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2621 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | |||||
chr12:122144454 | G | A | 2 | a0001c0008t0055 a0002c0002t0012 |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2642G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2642 | chr12 | 122144454 | ||||||
chr12:122144662 | G | A | 2 | a0001c0001t0033 a0002c0009t0069 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2850G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2850 | chr12 | 122144662 | ||||||
chr12:122144737 | A | G | 1 | a0002c0002t0040 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2925A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2925 | chr12 | 122144737 | ||||||
chr12:122144865 | T | C | 1 | a0002c0004t0065 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3053T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3053 | chr12 | 122144865 | ||||||
chr12:122144914 | A | G | 1 | a0001c0001t0063 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3102A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3102 | chr12 | 122144914 | ||||||
chr12:122145069 | T | C | 1 | a0001c0001t0031 | 2 | HG02083.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3257T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3257 | chr12 | 122145069 | ||||||
chr12:122145260 | G | A | 1 | a0002c0002t0038 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3448G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3448 | chr12 | 122145260 | ||||||
chr12:122145317 | A | G | 58 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(55): Show |
192 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3505A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3505 | chr12 | 122145317 | ||||||
chr12:122145323 | C | T | 3 | a0005c0012t0072 a0005c0012t0073 a0010c0021t0076 |
3 | HG02895.hp1 HG02922.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3511C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3511 | chr12 | 122145323 | ||||||
chr12:122145328 | A | G | 32 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(29): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3516A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3516 | chr12 | 122145328 | ||||||
chr12:122145462 | G | T | 62 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0020 others(59): Show |
192 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3650G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3650 | chr12 | 122145462 | ||||||
chr12:122145738 | G | A | 32 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(29): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3926G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3926 | chr12 | 122145738 | ||||||
chr12:122145769 | G | C | 1 | a0004c0007t0074 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3957G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3957 | chr12 | 122145769 | ||||||
chr12:122145786 | G | A | 8 | a0004c0007t0019 a0004c0007t0034 a0004c0007t0074 others(5): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3974G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3974 | chr12 | 122145786 | ||||||
chr12:122145803 | C | T | 1 | a0002c0004t0052 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3991C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3991 | chr12 | 122145803 | ||||||
chr12:122145855 | C | T | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4043C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4043 | chr12 | 122145855 | ||||||
chr12:122145928 | C | T | 1 | a0001c0001t0043 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4116C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4116 | chr12 | 122145928 | ||||||
chr12:122145947 | G | A | 1 | a0001c0001t0057 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4135 | chr12 | 122145947 | ||||||
chr12:122146106 | G | C | 1 | a0002c0005t0009 | 5 | HG00323.hp1 HG01099.hp1 HG01109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4294G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4294 | chr12 | 122146106 | ||||||
chr12:122146146 | T | C | 6 | a0004c0007t0019 a0004c0007t0034 a0004c0007t0074 others(3): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4334T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4334 | chr12 | 122146146 | ||||||
chr12:122146181 | G | A | 1 | a0001c0008t0047 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4369G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4369 | chr12 | 122146181 | ||||||
chr12:122146362 | G | A | 57 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(54): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*4550G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4550 | chr12 | 122146362 | ||||||
chr12:122146368 | C | T | 56 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(53): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*4556C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4556 | chr12 | 122146368 | ||||||
chr12:122146371 | A | G | 1 | a0001c0003t0046 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4559A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4559 | chr12 | 122146371 | ||||||
chr12:122146408 | C | T | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4596C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4596 | chr12 | 122146408 | ||||||
chr12:122146414 | C | T | 1 | a0002c0010t0017 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4602C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4602 | chr12 | 122146414 | ||||||
chr12:122146439 | C | T | 1 | a0001c0008t0028 | 2 | HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4627C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4627 | chr12 | 122146439 | ||||||
chr12:122146559 | A | G | 7 | a0002c0002t0005 a0002c0002t0012 a0002c0004t0005 others(4): Show |
23 | HG01243.hp2 HG01884.hp1 HG01993.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4747A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4747 | chr12 | 122146559 | ||||||
chr12:122146574 | G | A | 1 | a0002c0004t0048 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4762G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4762 | chr12 | 122146574 | ||||||
chr12:122146621 | CGT | C | 37 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(34): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*4827_*4828delTG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4827 | INFO_REALIGN_3_PRIME | chr12 | 122146621 | |||||
chr12:122146621 | CGTGT | C | 2 | a0001c0001t0022 a0001c0001t0058 |
4 | HG03490.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4825_*4828delTGTG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4825 | INFO_REALIGN_3_PRIME | chr12 | 122146621 | |||||
chr12:122146641 | C | T | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4829C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4829 | chr12 | 122146641 | ||||||
chr12:122146642 | A | G | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4830A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4830 | chr12 | 122146642 | ||||||
chr12:122146642 | ACG | A | 23 | a0001c0001t0061 a0001c0003t0003 a0001c0003t0004 others(20): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*4837_*4838delCG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4837 | INFO_REALIGN_3_PRIME | chr12 | 122146642 | |||||
chr12:122146644 | G | A | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4832G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4832 | chr12 | 122146644 | ||||||
chr12:122146646 | G | A | 5 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0065 others(2): Show |
17 | HG01993.hp1 HG02109.hp2 HG02129.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4834G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4834 | chr12 | 122146646 | ||||||
chr12:122146661 | G | T | 67 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(64): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*4849G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4849 | chr12 | 122146661 | ||||||
chr12:122146701 | G | A | 1 | a0001c0008t0028 | 2 | HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4889G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4889 | chr12 | 122146701 | ||||||
chr12:122146737 | TGGTTCTG others(15): Show |
T | 6 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0065 others(3): Show |
18 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4926_*4947delGGTT others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4926 | chr12 | 122146737 | ||||||
chr12:122146791 | T | C | 2 | a0001c0001t0043 a0001c0008t0047 |
2 | HG00597.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4979T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4979 | chr12 | 122146791 | ||||||
chr12:122146934 | C | T | 11 | a0001c0003t0004 a0001c0008t0028 a0001c0008t0055 others(8): Show |
27 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5122C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5122 | chr12 | 122146934 | ||||||
chr12:122146938 | T | G | 6 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0065 others(3): Show |
18 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5126T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5126 | chr12 | 122146938 | ||||||
chr12:122146945 | T | C | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5133T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5133 | chr12 | 122146945 | ||||||
chr12:122146980 | T | G | 1 | a0001c0003t0049 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5168T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5168 | chr12 | 122146980 | ||||||
chr12:122147006 | G | A | 1 | a0001c0001t0059 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5194G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5194 | chr12 | 122147006 | ||||||
chr12:122147046 | T | C | 2 | a0001c0001t0013 a0001c0001t0057 |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5234T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5234 | chr12 | 122147046 | ||||||
chr12:122147131 | G | C | 1 | a0010c0021t0076 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5319G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5319 | chr12 | 122147131 | ||||||
chr12:122147205 | T | C | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(49): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*5393T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5393 | chr12 | 122147205 | ||||||
chr12:122147255 | C | T | 12 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0065 others(9): Show |
25 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5443C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5443 | chr12 | 122147255 | ||||||
chr12:122147298 | C | G | 13 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0065 others(10): Show |
26 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5486C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5486 | chr12 | 122147298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:122079288 | T | C | 20 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(17): Show |
20 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+22T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079288 | |||||||
chr12:122079309 | T | C | 1 | a0002c0002t0005g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.413+43T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079309 | |||||||
chr12:122079331 | A | G | 1 | a0002c0002t0002g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+65A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079331 | |||||||
chr12:122079450 | T | A | 1 | a0002c0002t0002g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+184T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079450 | |||||||
chr12:122079489 | T | A | 1 | a0001c0001t0008g0028 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.413+223T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079489 | |||||||
chr12:122079567 | T | A | 1 | a0002c0002t0002g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+301T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079567 | |||||||
chr12:122079858 | T | C | 6 | a0003c0006t0001g0029 a0003c0006t0001g0030 a0003c0006t0001g0031 others(3): Show |
6 | HG02257.hp2 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+592T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079858 | |||||||
chr12:122079937 | A | C | 3 | a0001c0001t0013g0345 a0001c0001t0029g0343 a0001c0001t0057g0344 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+671A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079937 | |||||||
chr12:122080041 | T | C | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+775T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080041 | |||||||
chr12:122080123 | C | T | 1 | a0001c0001t0007g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.413+857C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080123 | |||||||
chr12:122080155 | T | C | 4 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(1): Show |
4 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+889T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080155 | |||||||
chr12:122080337 | A | G | 2 | a0002c0002t0002g0340 a0007c0023t0002g0341 |
2 | HG00323.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.413+1071A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080337 | |||||||
chr12:122080345 | A | G | 2 | a0001c0001t0031g0338 a0001c0001t0031g0339 |
2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.413+1079A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080345 | |||||||
chr12:122080482 | A | T | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1216A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080482 | |||||||
chr12:122080505 | C | T | 20 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(17): Show |
20 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1239C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080505 | |||||||
chr12:122080733 | G | T | 1 | a0001c0001t0006g0330 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.413+1467G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080733 | |||||||
chr12:122080953 | G | A | 1 | a0002c0027t0003g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413+1687G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080953 | |||||||
chr12:122081029 | CT | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.413+1765delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122081029 | ||||||
chr12:122081053 | A | G | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+1787A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081053 | |||||||
chr12:122081119 | C | G | 4 | a0002c0002t0002g0326 a0002c0002t0002g0327 a0002c0002t0002g0329 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+1853C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081119 | |||||||
chr12:122081182 | G | A | 10 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+1916G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081182 | |||||||
chr12:122081287 | G | A | 10 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+2021G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081287 | |||||||
chr12:122081427 | G | C | 3 | a0001c0001t0001g0051 a0001c0001t0042g0049 a0001c0001t0043g0050 |
3 | NA18982.hp2 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.413+2161G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081427 | |||||||
chr12:122081564 | T | C | 4 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(1): Show |
4 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+2298T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081564 | |||||||
chr12:122081755 | A | T | 3 | a0001c0001t0013g0345 a0001c0001t0029g0343 a0001c0001t0057g0344 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+2489A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081755 | |||||||
chr12:122081887 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+2621C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081887 | |||||||
chr12:122081945 | T | G | 4 | a0004c0007t0034g0331 a0004c0007t0034g0332 a0004c0007t0074g0334 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+2679T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081945 | |||||||
chr12:122082179 | G | T | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.413+2913G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082179 | |||||||
chr12:122082206 | C | T | 47 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.413+2940C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082206 | |||||||
chr12:122082244 | G | C | 1 | a0002c0002t0002g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+2978G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082244 | |||||||
chr12:122082245 | C | G | 1 | a0002c0002t0002g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+2979C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082245 | |||||||
chr12:122082287 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+3021C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082287 | |||||||
chr12:122082669 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.413+3403A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082669 | |||||||
chr12:122082672 | T | C | 3 | a0001c0001t0013g0345 a0001c0001t0029g0343 a0001c0001t0057g0344 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+3406T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082672 | |||||||
chr12:122082967 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+3701C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082967 | |||||||
chr12:122083076 | T | C | 20 | a0001c0003t0003g0282 a0001c0003t0003g0283 a0001c0003t0003g0284 others(17): Show |
20 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+3810T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083076 | |||||||
chr12:122083461 | C | G | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+4195C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083461 | |||||||
chr12:122083542 | G | A | 4 | a0002c0010t0017g0169 a0002c0010t0017g0170 a0002c0010t0017g0171 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+4276G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083542 | |||||||
chr12:122083571 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+4305T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083571 | |||||||
chr12:122083580 | A | G | 4 | a0002c0002t0002g0276 a0002c0002t0002g0277 a0002c0002t0002g0278 others(1): Show |
4 | HG01358.hp2 NA18947.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4314A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083580 | |||||||
chr12:122083643 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.413+4377A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083643 | |||||||
chr12:122083710 | G | T | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+4444G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083710 | |||||||
chr12:122084056 | G | A | 9 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(6): Show |
9 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+4790G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084056 | |||||||
chr12:122084144 | T | TTG | 20 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0178 others(17): Show |
20 | HG01433.hp2 HG01891.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.413+4926_413+4927d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | T | TTGTG | 9 | a0001c0001t0001g0060 a0001c0001t0001g0174 a0001c0001t0007g0342 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4924_413+4927d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | T | TTGTGTG | 4 | a0001c0001t0011g0054 a0001c0001t0011g0056 a0002c0004t0005g0007 others(1): Show |
4 | HG02129.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4922_413+4927d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0029g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.413+4916_413+4927d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0011g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+4912_413+4927d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTG | T | 86 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(83): Show |
87 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.413+4926_413+4927d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTG | T | 72 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0080 others(69): Show |
72 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.413+4924_413+4927d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTG | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.413+4922_413+4927d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(13): Show |
16 | HG00280.hp1 HG00735.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+4920_413+4927d others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTGT others(3): Show |
T | 2 | a0002c0002t0005g0041 a0002c0004t0068g0042 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.413+4918_413+4927d others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTGT others(5): Show |
T | 4 | a0002c0002t0010g0019 a0002c0002t0041g0020 a0002c0004t0005g0045 others(1): Show |
4 | HG02027.hp2 HG03704.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4916_413+4927d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTGT others(7): Show |
T | 15 | a0001c0001t0022g0161 a0001c0008t0028g0018 a0002c0002t0005g0027 others(12): Show |
15 | HG00621.hp2 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+4914_413+4927d others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084144 | TTGTGTGT others(11): Show |
T | 1 | a0007c0023t0002g0341 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.413+4910_413+4927d others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | ||||||
chr12:122084259 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.413+4993C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084259 | |||||||
chr12:122084295 | C | A | 1 | a0002c0009t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.413+5029C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084295 | |||||||
chr12:122084462 | G | A | 1 | a0002c0002t0038g0230 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.413+5196G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084462 | |||||||
chr12:122084477 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0154 others(4): Show |
7 | HG00280.hp1 HG00735.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+5211G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084477 | |||||||
chr12:122084607 | C | T | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+5341C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084607 | |||||||
chr12:122084705 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.413+5439C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084705 | |||||||
chr12:122084801 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.413+5535G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084801 | |||||||
chr12:122084815 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0188 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+5549T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084815 | |||||||
chr12:122084871 | C | G | 10 | a0001c0003t0003g0302 a0001c0003t0003g0303 a0001c0003t0003g0318 others(7): Show |
10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+5605C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084871 | |||||||
chr12:122084960 | C | T | 1 | a0002c0002t0002g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413+5694C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084960 | |||||||
chr12:122085014 | T | C | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+5748T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085014 | |||||||
chr12:122085015 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+5749T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085015 | |||||||
chr12:122085028 | G | C | 1 | a0002c0004t0003g0204 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.413+5762G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085028 | |||||||
chr12:122085266 | AC | A | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+6002delC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085266 | ||||||
chr12:122085405 | A | AT | 7 | a0001c0001t0001g0152 a0001c0001t0013g0345 a0001c0001t0014g0153 others(4): Show |
7 | HG02056.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+6155dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085405 | ||||||
chr12:122085405 | AT | A | 6 | a0001c0001t0014g0096 a0001c0001t0030g0058 a0001c0001t0033g0163 others(3): Show |
6 | HG01099.hp2 HG01169.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+6155delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085405 | ||||||
chr12:122085511 | C | T | 1 | a0009c0020t0019g0337 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+6245C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085511 | |||||||
chr12:122085555 | C | G | 1 | a0001c0008t0028g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413+6289C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085555 | |||||||
chr12:122085762 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.413+6496T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085762 | |||||||
chr12:122085778 | A | G | 1 | a0001c0001t0032g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.413+6512A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085778 | |||||||
chr12:122085841 | T | C | 5 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(2): Show |
5 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+6575T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085841 | |||||||
chr12:122085846 | A | G | 1 | a0002c0002t0002g0278 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.413+6580A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085846 | |||||||
chr12:122085895 | C | T | 2 | a0004c0007t0019g0335 a0009c0020t0019g0337 |
2 | HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.413+6629C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085895 | |||||||
chr12:122085944 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.413+6678C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085944 | |||||||
chr12:122085982 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.413+6716G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085982 | |||||||
chr12:122086087 | A | T | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6821A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086087 | |||||||
chr12:122086088 | A | T | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6822A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086088 | |||||||
chr12:122086089 | A | G | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6823A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086089 | |||||||
chr12:122086095 | G | A | 1 | a0002c0004t0020g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.413+6829G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086095 | |||||||
chr12:122086098 | A | C | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6832A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086098 | |||||||
chr12:122086101 | G | T | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6835G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086101 | |||||||
chr12:122086106 | T | G | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6840T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086106 | |||||||
chr12:122086110 | G | GAAGCCGG others(9): Show |
1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6844_413+6845i others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086110 | |||||||
chr12:122086112 | C | G | 1 | a0002c0002t0002g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6846C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086112 | |||||||
chr12:122086161 | TG | T | 3 | a0001c0001t0030g0058 a0002c0002t0002g0273 a0002c0005t0004g0231 |
3 | HG01169.hp2 HG03491.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.413+6898delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122086161 | ||||||
chr12:122086175 | C | G | 5 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+6909C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086175 | |||||||
chr12:122086289 | G | A | 1 | a0002c0005t0004g0275 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.413+7023G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086289 | |||||||
chr12:122086322 | GA | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.413+7057delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086322 | |||||||
chr12:122086363 | G | A | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+7097G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086363 | |||||||
chr12:122086693 | C | T | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+7427C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086693 | |||||||
chr12:122086876 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.413+7610A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086876 | |||||||
chr12:122086963 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.413+7697A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086963 | |||||||
chr12:122086991 | A | G | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+7725A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086991 | |||||||
chr12:122086995 | G | A | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7729G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086995 | |||||||
chr12:122086996 | C | T | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7730C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086996 | |||||||
chr12:122087008 | C | G | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+7742C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087008 | |||||||
chr12:122087020 | G | C | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7754G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087020 | |||||||
chr12:122087021 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0147 |
4 | HG00099.hp2 HG00140.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+7755T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087021 | |||||||
chr12:122087073 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+7807G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087073 | |||||||
chr12:122087095 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+7829C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087095 | |||||||
chr12:122087130 | C | T | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+7864C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087130 | |||||||
chr12:122087237 | C | T | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+7971C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087237 | |||||||
chr12:122087287 | C | T | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+8021C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087287 | |||||||
chr12:122087574 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.413+8308A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087574 | |||||||
chr12:122087632 | A | G | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+8366A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087632 | |||||||
chr12:122087648 | G | T | 1 | a0001c0001t0063g0146 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.413+8382G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087648 | |||||||
chr12:122087858 | G | GT | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+8597dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122087858 | ||||||
chr12:122087950 | A | G | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+8684A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087950 | |||||||
chr12:122087982 | G | A | 1 | a0002c0002t0002g0340 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.413+8716G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087982 | |||||||
chr12:122088009 | C | T | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+8743C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088009 | |||||||
chr12:122088130 | C | T | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+8864C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088130 | |||||||
chr12:122088131 | G | A | 1 | a0002c0005t0045g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.413+8865G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088131 | |||||||
chr12:122088135 | A | G | 1 | a0002c0002t0002g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.413+8869A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088135 | |||||||
chr12:122088171 | C | T | 1 | a0001c0001t0015g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.413+8905C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088171 | |||||||
chr12:122088313 | T | C | 1 | a0002c0002t0002g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.413+9047T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088313 | |||||||
chr12:122088381 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413+9115T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088381 | |||||||
chr12:122088470 | G | A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+9204G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088470 | |||||||
chr12:122088533 | A | G | 1 | a0002c0002t0016g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.413+9267A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088533 | |||||||
chr12:122088580 | A | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+9314A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088580 | |||||||
chr12:122088734 | C | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+9468C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088734 | |||||||
chr12:122088784 | C | T | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+9518C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088784 | |||||||
chr12:122088943 | G | A | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+9677G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088943 | |||||||
chr12:122089009 | C | CA | 51 | a0001c0001t0001g0092 a0001c0001t0001g0152 a0001c0001t0001g0154 others(48): Show |
52 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.413+9766dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089009 | ||||||
chr12:122089009 | CA | C | 46 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0174 others(43): Show |
46 | HG00323.hp1 HG00621.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.413+9766delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089009 | ||||||
chr12:122089053 | C | T | 1 | a0004c0007t0074g0334 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413+9787C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089053 | |||||||
chr12:122089210 | G | GAAGAAC | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+9945_413+9950d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089210 | ||||||
chr12:122089391 | A | G | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+10125A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089391 | |||||||
chr12:122089577 | A | G | 7 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+10311A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089577 | |||||||
chr12:122089952 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413+10686C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089952 | |||||||
chr12:122090080 | T | C | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+10814T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090080 | |||||||
chr12:122090119 | C | T | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.413+10853C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090119 | |||||||
chr12:122090283 | G | A | 2 | a0002c0002t0012g0210 a0002c0002t0012g0211 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.413+11017G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090283 | |||||||
chr12:122090294 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.413+11028G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090294 | |||||||
chr12:122090357 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.413+11091T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090357 | |||||||
chr12:122090369 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+11103T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090369 | |||||||
chr12:122090408 | ACT | A | 10 | a0001c0003t0003g0302 a0001c0003t0003g0303 a0001c0003t0003g0318 others(7): Show |
10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+11147_413+1114 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122090408 | ||||||
chr12:122090419 | A | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+11153A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090419 | |||||||
chr12:122090496 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.413+11242delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122090496 | ||||||
chr12:122090502 | A | G | 1 | a0002c0002t0012g0004 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.413+11236A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090502 | |||||||
chr12:122090554 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.413+11288A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090554 | |||||||
chr12:122090577 | A | G | 1 | a0004c0007t0019g0335 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+11311A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090577 | |||||||
chr12:122091073 | T | A | 1 | a0001c0003t0003g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.413+11807T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091073 | |||||||
chr12:122091193 | G | A | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+11927G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091193 | |||||||
chr12:122091416 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+12150G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091416 | |||||||
chr12:122091477 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.413+12211T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091477 | |||||||
chr12:122091642 | A | C | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+12376A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091642 | |||||||
chr12:122091700 | A | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+12434A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091700 | |||||||
chr12:122091761 | C | T | 1 | a0004c0007t0019g0335 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+12495C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091761 | |||||||
chr12:122092029 | C | T | 12 | a0001c0001t0001g0147 a0001c0008t0028g0016 a0001c0008t0028g0018 others(9): Show |
12 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+12763C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092029 | |||||||
chr12:122092059 | CCTTTCTT others(3): Show |
C | 2 | a0002c0002t0002g0267 a0002c0002t0002g0272 |
2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.413+12808_413+1281 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092059 | ||||||
chr12:122092107 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+12841C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092107 | |||||||
chr12:122092160 | C | T | 1 | a0011c0014t0019g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.413+12894C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092160 | |||||||
chr12:122092280 | G | A | 3 | a0002c0002t0002g0244 a0002c0002t0002g0245 a0002c0002t0002g0246 |
3 | NA18953.hp1 NA18972.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.413+13014G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092280 | |||||||
chr12:122092350 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+13084T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092350 | |||||||
chr12:122092386 | A | G | 1 | a0002c0010t0017g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.413+13120A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092386 | |||||||
chr12:122092518 | G | A | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+13252G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092518 | |||||||
chr12:122092742 | A | G | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+13476A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092742 | |||||||
chr12:122092847 | C | T | 221 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(218): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.413+13581C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092847 | |||||||
chr12:122092916 | T | TGATGTGT others(11): Show |
1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+13659_413+1366 others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092916 | ||||||
chr12:122092916 | T | TGATGTGT others(12): Show |
206 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(203): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.413+13659_413+1366 others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092916 | ||||||
chr12:122092925 | T | TTGGTGTG others(12): Show |
1 | a0012c0016t0003g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.413+13659_413+1366 others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092925 | |||||||
chr12:122093034 | GGT | G | 58 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(55): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+13777_413+1377 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093034 | ||||||
chr12:122093095 | TGTGGTGT others(5): Show |
T | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+13830_413+1384 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093095 | |||||||
chr12:122093178 | G | A | 1 | a0002c0002t0002g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.413+13912G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093178 | |||||||
chr12:122093256 | A | C | 1 | a0002c0005t0009g0239 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.413+13990A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093256 | |||||||
chr12:122093260 | Y | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0008g0028 others(11): Show |
15 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+13994C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093260 | |||||||
chr12:122093276 | A | G | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+14010A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093276 | |||||||
chr12:122093317 | G | A | 79 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(76): Show |
79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.413+14051G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093317 | |||||||
chr12:122093461 | A | G | 179 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(176): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.413+14195A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093461 | |||||||
chr12:122093464 | T | C | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+14198T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093464 | |||||||
chr12:122093485 | GGT | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14229_413+1423 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093485 | ||||||
chr12:122093498 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+14232G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093498 | |||||||
chr12:122093596 | G | A | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+14330G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093596 | |||||||
chr12:122093677 | A | G | 227 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0174 others(224): Show |
228 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.413+14411A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093677 | |||||||
chr12:122093697 | TGGGGTGT others(10): Show |
T | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+14442_413+1445 others(21): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093697 | ||||||
chr12:122093765 | T | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14499T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093765 | |||||||
chr12:122093767 | T | G | 179 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(176): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.413+14501T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093767 | |||||||
chr12:122093769 | T | G | 180 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(177): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+14503T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093769 | |||||||
chr12:122093791 | TGTGTGTG others(3): Show |
T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+14536_413+1454 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093791 | ||||||
chr12:122093854 | AGTGTCTG | A | 4 | a0002c0010t0017g0169 a0002c0010t0017g0170 a0002c0010t0017g0171 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+14593_413+1459 others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093854 | ||||||
chr12:122093890 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.413+14624C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093890 | |||||||
chr12:122093902 | G | C | 2 | a0001c0001t0008g0028 a0001c0001t0008g0081 |
2 | HG01167.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.413+14636G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093902 | |||||||
chr12:122093927 | TGTG | T | 81 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(78): Show |
81 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.413+14668_413+1467 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093927 | ||||||
chr12:122093980 | G | A | 180 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(177): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+14714G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093980 | |||||||
chr12:122093991 | C | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14725C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093991 | |||||||
chr12:122094001 | TGTG | T | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+14739_413+1474 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094001 | ||||||
chr12:122094095 | G | T | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+14829G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094095 | |||||||
chr12:122094128 | ATG | A | 58 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(55): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+14869_413+1487 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094128 | ||||||
chr12:122094176 | GTGT | G | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+14913_413+1491 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094176 | ||||||
chr12:122094192 | TGTGTGTT others(1): Show |
T | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+14933_413+1494 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094192 | ||||||
chr12:122094217 | GGT | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14958_413+1495 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094217 | ||||||
chr12:122094247 | TG | T | 180 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(177): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+14983delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094247 | ||||||
chr12:122094389 | GTGT | G | 3 | a0002c0005t0009g0233 a0002c0005t0009g0236 a0002c0005t0009g0239 |
3 | HG01109.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.413+15126_413+1512 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094389 | ||||||
chr12:122094391 | G | T | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15125G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094391 | |||||||
chr12:122094445 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15179C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094445 | |||||||
chr12:122094498 | CTG | C | 168 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(165): Show |
169 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.413+15241_413+1524 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094498 | ||||||
chr12:122094516 | GGT | G | 179 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(176): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.413+15259_413+1526 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094516 | ||||||
chr12:122094520 | T | A | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15254T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094520 | |||||||
chr12:122094550 | G | T | 1 | a0002c0002t0002g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.413+15284G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094550 | |||||||
chr12:122094574 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15308G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094574 | |||||||
chr12:122094599 | GTGT | G | 5 | a0002c0005t0009g0233 a0002c0005t0009g0236 a0002c0005t0009g0239 others(2): Show |
5 | HG00323.hp1 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+15337_413+1533 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094599 | ||||||
chr12:122094679 | C | T | 4 | a0002c0002t0012g0004 a0002c0002t0012g0210 a0002c0002t0012g0211 others(1): Show |
5 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+15413C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094679 | |||||||
chr12:122094681 | A | G | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+15415A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094681 | |||||||
chr12:122094803 | GGTGTGTT others(5): Show |
G | 1 | a0002c0002t0002g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.413+15555_413+1556 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094803 | ||||||
chr12:122094919 | G | T | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+15653G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094919 | |||||||
chr12:122094996 | G | A | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+15730G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094996 | |||||||
chr12:122094996 | G | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15730G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094996 | |||||||
chr12:122095001 | CTG | C | 181 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(178): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+15740_413+1574 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095001 | ||||||
chr12:122095145 | TGTGCGGT others(19): Show |
T | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+15905_413+1593 others(30): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095145 | ||||||
chr12:122095154 | T | A | 1 | a0001c0003t0007g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15888T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095154 | |||||||
chr12:122095155 | G | T | 1 | a0001c0003t0007g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15889G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095155 | |||||||
chr12:122095157 | T | C | 1 | a0001c0003t0007g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15891T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095157 | |||||||
chr12:122095160 | T | G | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15894T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095160 | |||||||
chr12:122095168 | G | A | 1 | a0001c0001t0006g0128 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.413+15902G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095168 | |||||||
chr12:122095171 | A | T | 1 | a0001c0003t0007g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15905A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095171 | |||||||
chr12:122095176 | G | A | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+15910G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095176 | |||||||
chr12:122095189 | G | A | 3 | a0002c0005t0009g0233 a0002c0005t0009g0236 a0002c0005t0009g0239 |
3 | HG01109.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.413+15923G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095189 | |||||||
chr12:122095201 | G | A | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+15935G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095201 | |||||||
chr12:122095297 | T | G | 1 | a0001c0001t0006g0330 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.413+16031T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095297 | |||||||
chr12:122095297 | T | TG | 18 | a0001c0001t0001g0107 a0001c0001t0013g0345 a0001c0001t0033g0163 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+16038dupG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095297 | ||||||
chr12:122095299 | G | T | 3 | a0002c0002t0002g0200 a0002c0002t0002g0266 a0010c0021t0076g0012 |
3 | HG02523.hp2 HG03579.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.413+16033G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095299 | |||||||
chr12:122095303 | G | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+16037G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095303 | |||||||
chr12:122095305 | T | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+16039T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095305 | |||||||
chr12:122095342 | G | C | 208 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(205): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.413+16076G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095342 | |||||||
chr12:122095478 | G | A | 10 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+16212G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095478 | |||||||
chr12:122095558 | G | A | 1 | a0001c0003t0003g0307 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.413+16292G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095558 | |||||||
chr12:122095675 | CCTTTT | C | 12 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+16416_413+1642 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095675 | ||||||
chr12:122095782 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+16516C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095782 | |||||||
chr12:122095877 | T | A | 12 | a0002c0002t0002g0198 a0002c0002t0002g0199 a0002c0002t0010g0019 others(9): Show |
12 | HG00621.hp2 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+16611T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095877 | |||||||
chr12:122095897 | G | A | 46 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(43): Show |
46 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.413+16631G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095897 | |||||||
chr12:122095951 | G | C | 8 | a0003c0006t0001g0029 a0003c0006t0001g0030 a0003c0006t0001g0031 others(5): Show |
8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+16685G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095951 | |||||||
chr12:122095959 | G | A | 180 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(177): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+16693G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095959 | |||||||
chr12:122096185 | G | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.413+16919G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096185 | |||||||
chr12:122096235 | A | G | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+16969A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096235 | |||||||
chr12:122096282 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+17016A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096282 | |||||||
chr12:122096557 | A | G | 1 | a0004c0007t0074g0334 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413+17291A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096557 | |||||||
chr12:122096601 | G | A | 10 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+17335G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096601 | |||||||
chr12:122096775 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+17509G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096775 | |||||||
chr12:122096881 | G | A | 1 | a0001c0001t0011g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.413+17615G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096881 | |||||||
chr12:122096925 | G | A | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+17659G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096925 | |||||||
chr12:122097064 | C | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+17798C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097064 | |||||||
chr12:122097222 | A | G | 1 | a0001c0001t0014g0153 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.413+17956A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097222 | |||||||
chr12:122097239 | C | T | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+17973C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097239 | |||||||
chr12:122097248 | G | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+17982G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097248 | |||||||
chr12:122097279 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18013C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097279 | |||||||
chr12:122097584 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0075 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+18318G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097584 | |||||||
chr12:122097594 | CAG | C | 5 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+18331_413+1833 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097594 | ||||||
chr12:122097613 | T | TA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.413+18361dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097613 | ||||||
chr12:122097676 | G | GT | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+18411dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097676 | ||||||
chr12:122097692 | C | T | 4 | a0004c0007t0034g0331 a0004c0007t0034g0332 a0004c0007t0074g0334 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+18426C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097692 | |||||||
chr12:122097746 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.413+18480G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097746 | |||||||
chr12:122097846 | T | TC | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(133): Show |
140 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+18585dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097846 | ||||||
chr12:122097846 | T | TCC | 8 | a0001c0001t0001g0060 a0001c0001t0001g0150 a0001c0001t0014g0069 others(5): Show |
8 | HG01175.hp2 HG02738.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+18584_413+1858 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097846 | ||||||
chr12:122097852 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18586T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097852 | |||||||
chr12:122097857 | A | C | 1 | a0001c0001t0013g0345 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.413+18591A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097857 | |||||||
chr12:122097891 | G | C | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+18625G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097891 | |||||||
chr12:122097946 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18680T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097946 | |||||||
chr12:122097982 | T | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.413+18716T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097982 | |||||||
chr12:122098279 | A | T | 1 | a0005c0012t0072g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.413+19013A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098279 | |||||||
chr12:122098924 | G | A | 1 | a0001c0001t0059g0072 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.413+19658G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098924 | |||||||
chr12:122098971 | C | T | 1 | a0002c0002t0039g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.413+19705C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098971 | |||||||
chr12:122098980 | G | A | 58 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(55): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+19714G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098980 | |||||||
chr12:122099234 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.413+19968A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099234 | |||||||
chr12:122099252 | A | G | 3 | a0002c0002t0002g0326 a0002c0002t0002g0329 a0002c0024t0002g0328 |
3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.413+19986A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099252 | |||||||
chr12:122099375 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.413+20109T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099375 | |||||||
chr12:122099443 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+20177C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099443 | |||||||
chr12:122099451 | G | A | 1 | a0002c0004t0067g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.413+20185G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099451 | |||||||
chr12:122099616 | A | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+20350A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099616 | |||||||
chr12:122099720 | A | G | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+20454A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099720 | |||||||
chr12:122099744 | A | G | 1 | a0001c0008t0028g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.413+20478A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099744 | |||||||
chr12:122099823 | T | A | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+20557T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099823 | |||||||
chr12:122100178 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+20912T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100178 | |||||||
chr12:122100456 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+21190A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100456 | |||||||
chr12:122100518 | T | C | 3 | a0002c0004t0005g0045 a0002c0004t0005g0048 a0002c0004t0065g0047 |
3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+21252T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100518 | |||||||
chr12:122100634 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.413+21368A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100634 | |||||||
chr12:122100706 | T | C | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+21440T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100706 | |||||||
chr12:122101036 | A | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+21770A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101036 | |||||||
chr12:122101037 | TTATAA | T | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+21776_413+2178 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101037 | ||||||
chr12:122101106 | C | T | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+21840C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101106 | |||||||
chr12:122101144 | G | A | 1 | a0004c0007t0019g0335 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+21878G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101144 | |||||||
chr12:122101362 | A | G | 1 | a0001c0001t0006g0141 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.413+22096A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101362 | |||||||
chr12:122101374 | A | G | 10 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+22108A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101374 | |||||||
chr12:122101443 | A | G | 2 | a0002c0002t0027g0014 a0002c0002t0027g0015 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.413+22177A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101443 | |||||||
chr12:122101449 | C | CT | 69 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(66): Show |
69 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.413+22192dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101449 | ||||||
chr12:122101526 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.413+22260T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101526 | |||||||
chr12:122101554 | ATTTATTT others(6): Show |
A | 3 | a0002c0002t0026g0187 a0002c0002t0026g0202 a0002c0002t0044g0203 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.413+22292_413+2230 others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101554 | ||||||
chr12:122101566 | A | T | 5 | a0001c0003t0003g0312 a0001c0003t0003g0313 a0001c0003t0003g0314 others(2): Show |
5 | HG00741.hp2 HG01943.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+22300A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101566 | |||||||
chr12:122101566 | AT | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.413+22307delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101566 | ||||||
chr12:122101570 | T | A | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22304T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101570 | |||||||
chr12:122101573 | T | C | 1 | a0002c0002t0002g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22307T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101573 | |||||||
chr12:122101574 | C | CT | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+22317dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101574 | ||||||
chr12:122101574 | C | T | 1 | a0002c0002t0002g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22308C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101574 | |||||||
chr12:122101584 | C | CT | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.413+22332dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101584 | ||||||
chr12:122101584 | C | T | 1 | a0002c0002t0002g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22318C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101584 | |||||||
chr12:122101605 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+22339G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101605 | |||||||
chr12:122101641 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+22375C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101641 | |||||||
chr12:122101673 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+22407C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101673 | |||||||
chr12:122101674 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+22408A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101674 | |||||||
chr12:122101732 | C | CT | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22466_413+2246 others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101732 | |||||||
chr12:122101733 | A | C | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22467A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101733 | |||||||
chr12:122101743 | G | A | 1 | a0002c0002t0002g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22477G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101743 | |||||||
chr12:122101778 | A | G | 10 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+22512A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101778 | |||||||
chr12:122101858 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.413+22592C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101858 | |||||||
chr12:122102119 | G | A | 1 | a0002c0002t0010g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.413+22853G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102119 | |||||||
chr12:122102370 | G | A | 1 | a0001c0003t0003g0282 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.413+23104G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102370 | |||||||
chr12:122102413 | G | C | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+23147G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102413 | |||||||
chr12:122102430 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23164A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102430 | |||||||
chr12:122102645 | T | C | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+23379T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102645 | |||||||
chr12:122102754 | C | G | 3 | a0002c0002t0002g0199 a0002c0002t0016g0177 a0002c0002t0016g0186 |
3 | HG01070.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.413+23488C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102754 | |||||||
chr12:122102909 | G | A | 1 | a0001c0003t0049g0308 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413+23643G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102909 | |||||||
chr12:122102958 | T | G | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+23692T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102958 | |||||||
chr12:122102998 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+23732C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102998 | |||||||
chr12:122103026 | C | T | 1 | a0011c0014t0019g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.413+23760C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103026 | |||||||
chr12:122103054 | A | G | 70 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.413+23788A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103054 | |||||||
chr12:122103130 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23864A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103130 | |||||||
chr12:122103175 | ATATG | A | 51 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.413+23933_413+2393 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103175 | ||||||
chr12:122103187 | G | A | 1 | a0002c0002t0039g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.413+23921G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103187 | |||||||
chr12:122103194 | T | C | 1 | a0002c0002t0002g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413+23928T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103194 | |||||||
chr12:122103195 | GTATGTAT others(1): Show |
G | 8 | a0002c0002t0002g0279 a0002c0002t0026g0187 a0002c0002t0026g0202 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+23933_413+2394 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103195 | ||||||
chr12:122103199 | G | T | 2 | a0002c0002t0002g0221 a0002c0002t0002g0272 |
2 | HG03239.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.413+23933G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103199 | |||||||
chr12:122103199 | GTATT | G | 23 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(20): Show |
24 | HG01261.hp2 HG01884.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+23971_413+2397 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103199 | GTATTTAT others(1): Show |
G | 87 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0008g0148 others(84): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.413+23967_413+2397 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103199 | GTATTTAT others(5): Show |
G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+23963_413+2397 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103199 | GTATTTAT others(9): Show |
G | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+23959_413+2397 others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103199 | GTATTTAT others(13): Show |
G | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+23955_413+2397 others(24): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103199 | GTATTTAT others(17): Show |
G | 1 | a0001c0001t0014g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.413+23951_413+2397 others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | ||||||
chr12:122103203 | T | G | 4 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0001c0001t0057g0344 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+23937T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103203 | |||||||
chr12:122103207 | T | G | 18 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(15): Show |
19 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+23941T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103207 | |||||||
chr12:122103211 | T | G | 25 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0008g0148 others(22): Show |
25 | HG00099.hp1 HG00738.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.413+23945T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103211 | |||||||
chr12:122103215 | T | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.413+23949T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103215 | |||||||
chr12:122103219 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+23953T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103219 | |||||||
chr12:122103223 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413+23957T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103223 | |||||||
chr12:122103227 | T | G | 13 | a0001c0001t0033g0164 a0002c0002t0005g0027 a0002c0002t0005g0041 others(10): Show |
13 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+23961T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103227 | |||||||
chr12:122103231 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+23965T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103231 | |||||||
chr12:122103246 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23980G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103246 | |||||||
chr12:122103521 | C | CT | 20 | a0001c0003t0003g0299 a0001c0003t0003g0311 a0001c0003t0003g0322 others(17): Show |
20 | HG01099.hp1 HG01981.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-23718dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103521 | ||||||
chr12:122103521 | CT | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.414-23718delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103521 | ||||||
chr12:122103584 | G | A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-23672G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103584 | |||||||
chr12:122103690 | TTG | T | 7 | a0001c0003t0003g0006 a0001c0003t0003g0304 a0001c0003t0003g0306 others(4): Show |
7 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-23564_414-2356 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103690 | ||||||
chr12:122103694 | A | AT | 11 | a0002c0002t0002g0245 a0002c0002t0002g0340 a0002c0002t0010g0019 others(8): Show |
11 | HG00323.hp2 HG00621.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-23546dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103694 | ||||||
chr12:122103694 | A | T | 7 | a0001c0003t0003g0006 a0001c0003t0003g0304 a0001c0003t0003g0306 others(4): Show |
7 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-23562A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103694 | |||||||
chr12:122103746 | G | A | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-23510G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103746 | |||||||
chr12:122103776 | G | A | 3 | a0001c0003t0003g0312 a0001c0003t0003g0313 a0001c0003t0003g0314 |
3 | HG00741.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.414-23480G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103776 | |||||||
chr12:122103840 | G | GT | 24 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(21): Show |
25 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.414-23401dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103840 | ||||||
chr12:122103840 | GT | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.414-23401delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103840 | ||||||
chr12:122103844 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-23412T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103844 | |||||||
chr12:122103921 | C | T | 3 | a0002c0002t0010g0019 a0002c0002t0010g0024 a0002c0002t0010g0025 |
3 | HG02027.hp2 NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.414-23335C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103921 | |||||||
chr12:122103942 | G | A | 31 | a0002c0002t0021g0181 a0002c0004t0003g0176 a0002c0004t0003g0183 others(28): Show |
31 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.414-23314G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103942 | |||||||
chr12:122104026 | A | G | 1 | a0001c0008t0047g0289 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.414-23230A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104026 | |||||||
chr12:122104194 | A | ACAAGTGT others(3): Show |
2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-23061_414-2305 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104194 | ||||||
chr12:122104424 | G | A | 1 | a0001c0001t0031g0339 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.414-22832G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104424 | |||||||
chr12:122104485 | T | A | 3 | a0002c0002t0002g0221 a0002c0002t0002g0248 a0002c0002t0002g0253 |
3 | NA18952.hp1 NA19001.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.414-22771T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104485 | |||||||
chr12:122104509 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-22747G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104509 | |||||||
chr12:122104537 | C | A | 1 | a0002c0002t0002g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-22719C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104537 | |||||||
chr12:122104575 | C | CT | 7 | a0001c0003t0003g0298 a0001c0003t0003g0307 a0002c0002t0002g0245 others(4): Show |
7 | HG00673.hp1 HG01952.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-22659dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | ||||||
chr12:122104575 | CT | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-22659delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | ||||||
chr12:122104575 | CTT | C | 15 | a0001c0001t0008g0165 a0001c0001t0030g0059 a0002c0002t0041g0020 others(12): Show |
15 | HG01069.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-22660_414-2265 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | ||||||
chr12:122104575 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.414-22672_414-2265 others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | ||||||
chr12:122104602 | C | T | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-22654C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104602 | |||||||
chr12:122104609 | T | G | 2 | a0001c0001t0030g0058 a0001c0001t0030g0059 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.414-22647T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104609 | |||||||
chr12:122104653 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0015g0175 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.414-22603C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104653 | |||||||
chr12:122104675 | G | A | 2 | a0002c0002t0021g0181 a0002c0004t0021g0182 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-22581G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104675 | |||||||
chr12:122104681 | G | A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-22575G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104681 | |||||||
chr12:122104715 | G | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-22541G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104715 | |||||||
chr12:122104736 | C | T | 1 | a0002c0005t0009g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-22520C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104736 | |||||||
chr12:122104807 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-22449C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104807 | |||||||
chr12:122104848 | A | G | 70 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.414-22408A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104848 | |||||||
chr12:122104987 | G | A | 20 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-22269G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104987 | |||||||
chr12:122105234 | T | C | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-22022T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105234 | |||||||
chr12:122105278 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.414-21978G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105278 | |||||||
chr12:122105320 | A | AT | 6 | a0001c0001t0001g0136 a0001c0001t0011g0056 a0001c0001t0011g0061 others(3): Show |
6 | HG00609.hp2 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-21926dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122105320 | ||||||
chr12:122105350 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414-21906C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105350 | |||||||
chr12:122105353 | G | GT | 11 | a0001c0001t0006g0135 a0001c0001t0014g0134 a0001c0001t0043g0050 others(8): Show |
11 | HG02015.hp2 HG02080.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-21893dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122105353 | ||||||
chr12:122105377 | C | T | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.414-21879C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105377 | |||||||
chr12:122105564 | C | T | 1 | a0002c0002t0002g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.414-21692C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105564 | |||||||
chr12:122105628 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0147 |
4 | HG00099.hp2 HG00140.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-21628C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105628 | |||||||
chr12:122105633 | G | A | 3 | a0002c0004t0005g0045 a0002c0004t0005g0048 a0002c0004t0065g0047 |
3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.414-21623G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105633 | |||||||
chr12:122105791 | A | C | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-21465A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105791 | |||||||
chr12:122105821 | C | G | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-21435C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105821 | |||||||
chr12:122105918 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-21338G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105918 | |||||||
chr12:122105944 | G | C | 1 | a0011c0014t0019g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.414-21312G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105944 | |||||||
chr12:122105956 | A | C | 1 | a0002c0009t0011g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.414-21300A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105956 | |||||||
chr12:122105979 | C | T | 1 | a0002c0004t0020g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-21277C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105979 | |||||||
chr12:122106016 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-21240T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106016 | |||||||
chr12:122106037 | C | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-21219C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106037 | |||||||
chr12:122106090 | A | G | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-21166A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106090 | |||||||
chr12:122106176 | A | G | 21 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-21080A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106176 | |||||||
chr12:122106252 | T | TTC | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-21002_414-2100 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106252 | ||||||
chr12:122106440 | ATTGTCAC others(4): Show |
A | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-20805_414-2079 others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106440 | ||||||
chr12:122106491 | G | T | 4 | a0001c0003t0003g0006 a0001c0003t0003g0304 a0001c0003t0003g0306 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-20765G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106491 | |||||||
chr12:122106582 | G | A | 7 | a0002c0002t0026g0187 a0002c0002t0026g0202 a0002c0002t0044g0203 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-20674G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106582 | |||||||
chr12:122106588 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.414-20668G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106588 | |||||||
chr12:122106595 | C | CT | 17 | a0001c0001t0013g0037 a0001c0003t0003g0299 a0001c0003t0003g0303 others(14): Show |
17 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.414-20637dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | ||||||
chr12:122106595 | C | CTT | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-20638_414-2063 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | ||||||
chr12:122106595 | CT | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.414-20637delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | ||||||
chr12:122106595 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0056 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-20644_414-2063 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | ||||||
chr12:122106746 | C | T | 1 | a0002c0002t0002g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.414-20510C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106746 | |||||||
chr12:122106754 | T | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-20502T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106754 | |||||||
chr12:122106819 | C | A | 3 | a0002c0002t0026g0187 a0002c0002t0026g0202 a0002c0002t0044g0203 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.414-20437C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106819 | |||||||
chr12:122106860 | C | A | 1 | a0001c0001t0006g0114 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.414-20396C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106860 | |||||||
chr12:122106952 | G | C | 10 | a0001c0003t0003g0302 a0001c0003t0003g0303 a0001c0003t0003g0318 others(7): Show |
10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-20304G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106952 | |||||||
chr12:122106984 | G | A | 11 | a0001c0001t0001g0092 a0001c0001t0001g0113 a0001c0001t0001g0115 others(8): Show |
11 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-20272G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106984 | |||||||
chr12:122107007 | C | T | 20 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0077 others(17): Show |
20 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-20249C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107007 | |||||||
chr12:122107204 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-20052T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107204 | |||||||
chr12:122107466 | T | TG | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-19789dupG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122107466 | ||||||
chr12:122107556 | C | G | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-19700C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107556 | |||||||
chr12:122107602 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0130 |
3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-19654A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107602 | |||||||
chr12:122107944 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-19312C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107944 | |||||||
chr12:122108140 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-19116C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108140 | |||||||
chr12:122108346 | C | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-18910C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108346 | |||||||
chr12:122108367 | C | CA | 15 | a0001c0003t0003g0283 a0001c0003t0003g0290 a0001c0003t0003g0304 others(12): Show |
16 | HG01074.hp2 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.414-18868dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122108367 | ||||||
chr12:122108367 | CA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.414-18868delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122108367 | ||||||
chr12:122108495 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.414-18761C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108495 | |||||||
chr12:122108693 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414-18563G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108693 | |||||||
chr12:122108763 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-18493G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108763 | |||||||
chr12:122109224 | A | T | 1 | a0002c0004t0021g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414-18032A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109224 | |||||||
chr12:122109311 | C | T | 1 | a0002c0004t0004g0274 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414-17945C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109311 | |||||||
chr12:122109384 | A | C | 21 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-17872A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109384 | |||||||
chr12:122109486 | A | G | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-17770A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109486 | |||||||
chr12:122109697 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-17559C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109697 | |||||||
chr12:122109702 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-17554T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109702 | |||||||
chr12:122109982 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414-17274G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109982 | |||||||
chr12:122110026 | T | C | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-17230T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110026 | |||||||
chr12:122110191 | G | A | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-17065G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110191 | |||||||
chr12:122110299 | T | A | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-16957T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110299 | |||||||
chr12:122110348 | C | T | 1 | a0002c0004t0020g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-16908C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110348 | |||||||
chr12:122110374 | G | A | 2 | a0002c0004t0005g0017 a0002c0004t0066g0011 |
2 | NA18969.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.414-16882G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110374 | |||||||
chr12:122110444 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-16812C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110444 | |||||||
chr12:122110538 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-16718C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110538 | |||||||
chr12:122110544 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0007g0342 |
3 | HG02735.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.414-16712C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110544 | |||||||
chr12:122110638 | G | A | 1 | a0002c0004t0020g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-16618G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110638 | |||||||
chr12:122110806 | A | G | 3 | a0002c0002t0002g0243 a0002c0002t0002g0263 a0002c0002t0002g0268 |
3 | HG01975.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.414-16450A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110806 | |||||||
chr12:122110844 | A | G | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-16412A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110844 | |||||||
chr12:122110847 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-16409G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110847 | |||||||
chr12:122110884 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0077 |
2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.414-16372T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110884 | |||||||
chr12:122110893 | T | C | 2 | a0001c0001t0001g0150 a0002c0004t0020g0194 |
2 | HG02258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.414-16363T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110893 | |||||||
chr12:122110902 | C | A | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-16354C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110902 | |||||||
chr12:122111071 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-16185T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111071 | |||||||
chr12:122111076 | C | CA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.414-16162dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122111076 | ||||||
chr12:122111076 | CA | C | 63 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(60): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-16162delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122111076 | ||||||
chr12:122111335 | A | G | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-15921A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111335 | |||||||
chr12:122111564 | C | G | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-15692C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111564 | |||||||
chr12:122111601 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-15655C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111601 | |||||||
chr12:122111932 | A | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-15324A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111932 | |||||||
chr12:122112077 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-15179G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112077 | |||||||
chr12:122112136 | T | C | 2 | a0003c0006t0001g0030 a0003c0006t0001g0031 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.414-15120T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112136 | |||||||
chr12:122112351 | T | C | 1 | a0002c0002t0012g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-14905T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112351 | |||||||
chr12:122112399 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.414-14857G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112399 | |||||||
chr12:122112516 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0137 |
2 | NA18947.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.414-14740G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112516 | |||||||
chr12:122112519 | C | T | 8 | a0003c0006t0001g0029 a0003c0006t0001g0030 a0003c0006t0001g0031 others(5): Show |
8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-14737C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112519 | |||||||
chr12:122112527 | G | A | 7 | a0002c0004t0005g0007 a0002c0004t0005g0008 a0002c0004t0005g0009 others(4): Show |
7 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-14729G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112527 | |||||||
chr12:122112576 | G | A | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-14680G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112576 | |||||||
chr12:122112740 | G | A | 1 | a0002c0002t0002g0270 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.414-14516G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112740 | |||||||
chr12:122112863 | T | C | 1 | a0002c0004t0048g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.414-14393T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112863 | |||||||
chr12:122112976 | A | AG | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-14280_414-1427 others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112976 | |||||||
chr12:122113366 | C | G | 2 | a0002c0002t0021g0181 a0002c0004t0021g0182 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-13890C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113366 | |||||||
chr12:122113464 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-13792C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113464 | |||||||
chr12:122113513 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.414-13743C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113513 | |||||||
chr12:122113681 | C | CT | 6 | a0001c0003t0003g0284 a0001c0003t0046g0296 a0001c0008t0047g0289 others(3): Show |
6 | HG00597.hp2 HG02135.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-13554dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | C | CTTTT | 6 | a0004c0007t0019g0335 a0004c0007t0074g0334 a0004c0007t0075g0333 others(3): Show |
6 | HG01099.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-13557_414-1355 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | C | CTTTTT | 14 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-13558_414-1355 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | C | CTTTTTT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.414-13559_414-1355 others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | C | CTTTTTTT | 38 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0086 others(35): Show |
38 | HG00621.hp1 HG00735.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.414-13560_414-1355 others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | CT | C | 84 | a0001c0003t0003g0291 a0001c0008t0028g0016 a0001c0008t0028g0018 others(81): Show |
84 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-13554delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113681 | CTT | C | 6 | a0001c0008t0055g0215 a0002c0002t0002g0223 a0002c0002t0012g0004 others(3): Show |
7 | HG01169.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-13555_414-1355 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | ||||||
chr12:122113704 | A | G | 1 | a0002c0005t0004g0275 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.414-13552A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113704 | |||||||
chr12:122113714 | T | A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-13542T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113714 | |||||||
chr12:122113747 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-13509C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113747 | |||||||
chr12:122113798 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.414-13458C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113798 | |||||||
chr12:122113927 | C | T | 1 | a0001c0001t0011g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.414-13329C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113927 | |||||||
chr12:122113928 | G | A | 1 | a0001c0001t0063g0146 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.414-13328G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113928 | |||||||
chr12:122113981 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0075 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-13275G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113981 | |||||||
chr12:122113984 | C | CT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.414-13254dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | ||||||
chr12:122113984 | C | CTT | 9 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0006g0141 others(6): Show |
9 | HG00544.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-13255_414-1325 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | ||||||
chr12:122113984 | CT | C | 6 | a0001c0008t0055g0215 a0002c0002t0002g0340 a0002c0002t0012g0004 others(3): Show |
7 | HG00323.hp2 HG01516.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-13254delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | ||||||
chr12:122114047 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-13209A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114047 | |||||||
chr12:122114274 | C | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-12982C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114274 | |||||||
chr12:122114291 | C | A | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-12965C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114291 | |||||||
chr12:122114394 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12862T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114394 | |||||||
chr12:122114473 | A | G | 27 | a0002c0004t0003g0216 a0002c0004t0003g0217 a0002c0004t0004g0189 others(24): Show |
27 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.414-12783A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114473 | |||||||
chr12:122114495 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-12761T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114495 | |||||||
chr12:122114554 | G | A | 1 | a0002c0004t0020g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-12702G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114554 | |||||||
chr12:122114559 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-12697G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114559 | |||||||
chr12:122114668 | C | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-12588C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114668 | |||||||
chr12:122114689 | C | T | 1 | a0002c0005t0004g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.414-12567C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114689 | |||||||
chr12:122114712 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-12544T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114712 | |||||||
chr12:122114737 | C | CT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-12501dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122114737 | ||||||
chr12:122114737 | C | CTT | 6 | a0001c0001t0006g0109 a0001c0001t0006g0135 a0001c0001t0014g0153 others(3): Show |
6 | HG01175.hp2 HG02055.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-12502_414-1250 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122114737 | ||||||
chr12:122114755 | T | G | 5 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-12501T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114755 | |||||||
chr12:122114757 | G | T | 5 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-12499G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114757 | |||||||
chr12:122114758 | T | TTG | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.414-12498_414-1249 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114758 | |||||||
chr12:122114759 | G | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0007g0342 |
3 | HG02735.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.414-12497G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114759 | |||||||
chr12:122114764 | G | T | 1 | a0003c0006t0015g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414-12492G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114764 | |||||||
chr12:122114814 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12442C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114814 | |||||||
chr12:122114902 | C | T | 1 | a0002c0002t0002g0278 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.414-12354C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114902 | |||||||
chr12:122115006 | C | G | 20 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-12250C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115006 | |||||||
chr12:122115036 | C | T | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-12220C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115036 | |||||||
chr12:122115249 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12007C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115249 | |||||||
chr12:122115287 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-11969C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115287 | |||||||
chr12:122115294 | A | G | 20 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-11962A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115294 | |||||||
chr12:122115309 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-11947T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115309 | |||||||
chr12:122115388 | G | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-11868G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115388 | |||||||
chr12:122115416 | C | T | 4 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0001c0003t0003g0316 others(1): Show |
4 | HG02055.hp2 HG02129.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-11840C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115416 | |||||||
chr12:122115461 | C | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-11795C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115461 | |||||||
chr12:122115536 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11720G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115536 | |||||||
chr12:122115581 | T | G | 2 | a0002c0002t0027g0014 a0002c0002t0027g0015 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.414-11675T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115581 | |||||||
chr12:122115587 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.414-11669T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115587 | |||||||
chr12:122115587 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.414-11669T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115587 | |||||||
chr12:122115588 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.414-11668C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115588 | |||||||
chr12:122115588 | C | CA | 171 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(168): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.414-11651dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAA | 6 | a0001c0001t0008g0028 a0001c0001t0014g0134 a0001c0019t0001g0117 others(3): Show |
6 | HG01167.hp2 HG01496.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11652_414-1165 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.414-11653_414-1165 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAAA | 6 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0001t0006g0124 others(3): Show |
6 | HG02135.hp2 HG02738.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-11654_414-1165 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0013g0038 a0001c0001t0013g0039 a0001c0001t0013g0345 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-11660_414-1165 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAAAAAA others(4): Show |
9 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(6): Show |
9 | HG02809.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-11661_414-1165 others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAAAAAA others(5): Show |
9 | a0002c0004t0005g0044 a0002c0004t0005g0168 a0002c0004t0067g0173 others(6): Show |
9 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-11662_414-1165 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115588 | C | CAAAAAAA others(6): Show |
2 | a0002c0004t0065g0047 a0004c0007t0074g0334 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.414-11663_414-1165 others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | ||||||
chr12:122115610 | A | G | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-11646A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115610 | |||||||
chr12:122115966 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11290A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115966 | |||||||
chr12:122115985 | A | G | 1 | a0002c0002t0002g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-11271A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115985 | |||||||
chr12:122116019 | C | A | 12 | a0002c0005t0004g0231 a0002c0005t0004g0234 a0002c0005t0004g0237 others(9): Show |
12 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-11237C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116019 | |||||||
chr12:122116053 | A | AAC | 68 | a0001c0001t0057g0344 a0001c0003t0003g0293 a0001c0003t0020g0321 others(65): Show |
69 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.414-11169_414-1116 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACAC | 16 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(13): Show |
16 | HG01243.hp2 HG01261.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.414-11171_414-1116 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(3): Show |
5 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-11177_414-1116 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(5): Show |
4 | a0002c0004t0005g0045 a0002c0004t0005g0048 a0002c0004t0005g0168 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-11179_414-1116 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(7): Show |
6 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0004t0005g0046 others(3): Show |
6 | HG02145.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11181_414-1116 others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(9): Show |
1 | a0004c0007t0019g0335 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.414-11183_414-1116 others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(11): Show |
6 | a0004c0007t0034g0331 a0004c0007t0034g0332 a0004c0007t0074g0334 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11185_414-1116 others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | A | AACACACA others(17): Show |
1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-11191_414-1116 others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | AAC | A | 3 | a0002c0010t0017g0170 a0002c0010t0017g0171 a0002c0010t0017g0172 |
3 | HG01891.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.414-11169_414-1116 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | AACACAC | A | 3 | a0001c0001t0001g0174 a0001c0001t0014g0140 a0001c0001t0015g0175 |
3 | HG01257.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.414-11173_414-1116 others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116053 | AACACACA others(1): Show |
A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-11175_414-1116 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | ||||||
chr12:122116180 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-11076C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116180 | |||||||
chr12:122116256 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11000A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116256 | |||||||
chr12:122116281 | G | GT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-10966dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116281 | ||||||
chr12:122116421 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-10835T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116421 | |||||||
chr12:122116437 | C | A | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0112 others(5): Show |
8 | HG00280.hp1 HG00735.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-10819C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116437 | |||||||
chr12:122116693 | A | G | 1 | a0002c0002t0040g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.414-10563A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116693 | |||||||
chr12:122116742 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-10514A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116742 | |||||||
chr12:122117103 | C | T | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-10153C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117103 | |||||||
chr12:122117380 | A | G | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-9876A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117380 | |||||||
chr12:122117626 | G | C | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-9630G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117626 | |||||||
chr12:122117758 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-9498G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117758 | |||||||
chr12:122118053 | T | A | 1 | a0001c0003t0003g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.414-9203T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118053 | |||||||
chr12:122118094 | C | T | 1 | a0002c0002t0002g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.414-9162C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118094 | |||||||
chr12:122118263 | A | G | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-8993A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118263 | |||||||
chr12:122118270 | A | AT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.414-8983dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122118270 | ||||||
chr12:122118352 | C | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.414-8904C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118352 | |||||||
chr12:122118387 | C | T | 2 | a0002c0002t0023g0260 a0014c0022t0023g0261 |
2 | HG02155.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.414-8869C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118387 | |||||||
chr12:122118392 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8864T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118392 | |||||||
chr12:122118395 | A | G | 20 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-8861A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118395 | |||||||
chr12:122118576 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8680A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118576 | |||||||
chr12:122118709 | G | A | 1 | a0009c0020t0019g0337 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-8547G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118709 | |||||||
chr12:122118779 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8477C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118779 | |||||||
chr12:122118845 | C | CA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-8398dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122118845 | ||||||
chr12:122118866 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.414-8390T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118866 | |||||||
chr12:122118895 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.414-8361G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118895 | |||||||
chr12:122118932 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8324C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118932 | |||||||
chr12:122118933 | G | A | 1 | a0002c0004t0003g0183 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.414-8323G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118933 | |||||||
chr12:122118949 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0127 others(1): Show |
4 | HG01123.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-8307G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118949 | |||||||
chr12:122118967 | C | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-8289C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118967 | |||||||
chr12:122118993 | C | T | 7 | a0001c0001t0011g0056 a0001c0001t0011g0061 a0001c0001t0011g0064 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-8263C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118993 | |||||||
chr12:122119016 | A | T | 6 | a0001c0001t0008g0105 a0001c0001t0018g0082 a0001c0001t0018g0083 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-8240A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119016 | |||||||
chr12:122119034 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8222C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119034 | |||||||
chr12:122119037 | C | T | 2 | a0002c0002t0040g0262 a0002c0005t0004g0234 |
2 | HG01361.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.414-8219C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119037 | |||||||
chr12:122119167 | C | CA | 4 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0001c0003t0046g0296 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-8082dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119167 | ||||||
chr12:122119175 | CAAACA | C | 13 | a0002c0002t0002g0340 a0002c0002t0005g0027 a0002c0002t0005g0041 others(10): Show |
13 | HG00323.hp2 HG01243.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-8058_414-8054d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119175 | ||||||
chr12:122119190 | AAAACAAA others(2): Show |
A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-8058_414-8050d others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119190 | ||||||
chr12:122119315 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-7941G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119315 | |||||||
chr12:122119342 | T | A | 5 | a0001c0001t0011g0056 a0001c0001t0011g0061 a0001c0001t0011g0064 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-7914T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119342 | |||||||
chr12:122119431 | G | A | 8 | a0002c0002t0016g0269 a0004c0007t0019g0335 a0004c0007t0034g0331 others(5): Show |
8 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-7825G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119431 | |||||||
chr12:122119548 | C | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-7708C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119548 | |||||||
chr12:122119552 | C | T | 3 | a0002c0004t0005g0045 a0002c0004t0005g0048 a0002c0004t0065g0047 |
3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.414-7704C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119552 | |||||||
chr12:122119565 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7691G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119565 | |||||||
chr12:122119593 | G | A | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-7663G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119593 | |||||||
chr12:122119613 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7643G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119613 | |||||||
chr12:122119681 | G | A | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-7575G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119681 | |||||||
chr12:122119686 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7570T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119686 | |||||||
chr12:122119690 | G | A | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-7566G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119690 | |||||||
chr12:122119892 | TTGCCCTT others(8): Show |
T | 1 | a0002c0002t0002g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.414-7363_414-7349d others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119892 | |||||||
chr12:122120111 | A | G | 75 | a0001c0008t0055g0215 a0002c0002t0002g0005 a0002c0002t0002g0197 others(72): Show |
76 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.414-7145A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120111 | |||||||
chr12:122120171 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-7085_414-7084i others(3): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120171 | |||||||
chr12:122120250 | T | A | 1 | a0001c0001t0061g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.414-7006T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120250 | |||||||
chr12:122120299 | T | G | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-6957T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120299 | |||||||
chr12:122120341 | G | C | 1 | a0002c0002t0002g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.414-6915G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120341 | |||||||
chr12:122120402 | T | C | 2 | a0002c0002t0026g0202 a0002c0002t0044g0203 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.414-6854T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120402 | |||||||
chr12:122120404 | G | A | 20 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-6852G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120404 | |||||||
chr12:122120600 | A | G | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-6656A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120600 | |||||||
chr12:122120657 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-6599A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120657 | |||||||
chr12:122120750 | G | A | 1 | a0002c0002t0002g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.414-6506G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120750 | |||||||
chr12:122120778 | T | A | 1 | a0002c0005t0009g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-6478T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120778 | |||||||
chr12:122120972 | G | A | 93 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(90): Show |
94 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-6284G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120972 | |||||||
chr12:122120994 | G | A | 3 | a0002c0010t0017g0169 a0002c0010t0017g0170 a0002c0010t0017g0172 |
3 | HG01891.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.414-6262G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120994 | |||||||
chr12:122121009 | G | GTTTTTT | 13 | a0001c0001t0001g0133 a0001c0001t0007g0342 a0001c0001t0013g0036 others(10): Show |
13 | HG01515.hp2 HG02083.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | |||||||
chr12:122121009 | G | GTTTTTTT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | |||||||
chr12:122121009 | G | GTTTTTTT others(1): Show |
27 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0116 others(24): Show |
27 | HG00609.hp2 HG00735.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | |||||||
chr12:122121010 | G | GTTTTT | 7 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(4): Show |
8 | HG01261.hp2 HG01884.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-6232_414-6228d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(3): Show |
1 | a0002c0002t0071g0021 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.414-6237_414-6228d others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(4): Show |
2 | a0002c0002t0026g0202 a0002c0002t0044g0203 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.414-6238_414-6228d others(13): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(5): Show |
3 | a0002c0010t0017g0169 a0002c0010t0017g0171 a0002c0010t0017g0172 |
3 | HG02615.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.414-6239_414-6228d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(6): Show |
1 | a0002c0010t0017g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.414-6240_414-6228d others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(10): Show |
1 | a0002c0002t0027g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.414-6244_414-6228d others(19): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(11): Show |
6 | a0002c0002t0002g0326 a0002c0002t0005g0027 a0002c0002t0005g0041 others(3): Show |
6 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-6245_414-6228d others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(12): Show |
3 | a0002c0002t0002g0256 a0002c0002t0002g0329 a0002c0004t0068g0042 |
3 | HG02040.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(21): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(13): Show |
3 | a0002c0004t0005g0044 a0002c0004t0005g0046 a0002c0004t0005g0048 |
3 | HG02109.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(14): Show |
4 | a0002c0002t0016g0269 a0002c0004t0005g0168 a0002c0004t0065g0047 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(15): Show |
12 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0002g0243 others(9): Show |
12 | HG01358.hp2 HG01975.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(24): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(16): Show |
5 | a0002c0002t0002g0327 a0002c0002t0010g0022 a0002c0002t0041g0020 others(2): Show |
5 | HG03516.hp1 HG03704.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(25): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(17): Show |
11 | a0002c0002t0002g0005 a0002c0002t0002g0223 a0002c0002t0002g0271 others(8): Show |
11 | HG00544.hp1 HG00558.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(26): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(18): Show |
13 | a0002c0002t0002g0197 a0002c0002t0002g0221 a0002c0002t0002g0224 others(10): Show |
13 | HG00609.hp1 HG01167.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(27): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(19): Show |
3 | a0002c0002t0002g0225 a0002c0002t0002g0248 a0002c0002t0002g0253 |
3 | NA18952.hp1 NA19001.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(20): Show |
2 | a0002c0002t0002g0200 a0002c0002t0002g0255 |
2 | HG02523.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(29): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(21): Show |
2 | a0002c0002t0002g0220 a0002c0002t0010g0019 |
2 | HG02027.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(30): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(22): Show |
2 | a0002c0002t0016g0177 a0006c0013t0002g0229 |
2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(31): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(23): Show |
5 | a0002c0002t0002g0222 a0002c0002t0002g0227 a0002c0002t0002g0247 others(2): Show |
5 | HG01074.hp2 HG01433.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(32): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(24): Show |
2 | a0002c0002t0002g0198 a0002c0004t0066g0011 |
2 | HG01081.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(33): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(25): Show |
1 | a0002c0002t0010g0025 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(34): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(27): Show |
3 | a0002c0002t0002g0249 a0002c0002t0002g0273 a0002c0002t0040g0262 |
3 | HG03688.hp2 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(32): Show |
1 | a0002c0002t0002g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(41): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(34): Show |
1 | a0002c0002t0002g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.414-6228_414-6227i others(43): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(35): Show |
2 | a0002c0002t0002g0259 a0002c0002t0002g0279 |
2 | HG04228.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(44): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(38): Show |
1 | a0002c0002t0039g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(47): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(40): Show |
1 | a0002c0002t0002g0244 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(49): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | GTTTTTTT others(50): Show |
1 | a0002c0002t0002g0246 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(59): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.414-6246G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121010 | |||||||
chr12:122121010 | GT | G | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-6228delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121010 | GTTTT | G | 25 | a0002c0004t0003g0216 a0002c0004t0003g0217 a0002c0004t0004g0189 others(22): Show |
25 | HG01069.hp1 HG01099.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.414-6231_414-6228d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | ||||||
chr12:122121050 | G | T | 4 | a0001c0001t0014g0069 a0001c0001t0022g0076 a0001c0001t0022g0161 others(1): Show |
4 | HG03490.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-6206G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121050 | |||||||
chr12:122121140 | G | T | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-6116G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121140 | |||||||
chr12:122121157 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-6099A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121157 | |||||||
chr12:122121299 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-5957T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121299 | |||||||
chr12:122121307 | C | CT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-5928dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | ||||||
chr12:122121307 | C | CTT | 13 | a0001c0001t0001g0080 a0001c0001t0001g0138 a0001c0001t0001g0152 others(10): Show |
13 | HG00544.hp2 HG02109.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-5929_414-5928d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | ||||||
chr12:122121307 | CT | C | 8 | a0001c0003t0003g0282 a0001c0003t0003g0299 a0001c0003t0003g0306 others(5): Show |
8 | HG01070.hp1 HG01169.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-5928delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | ||||||
chr12:122121329 | A | T | 4 | a0002c0002t0012g0004 a0002c0002t0012g0210 a0002c0002t0012g0211 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-5927A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121329 | |||||||
chr12:122121376 | C | T | 94 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(91): Show |
95 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.414-5880C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121376 | |||||||
chr12:122121402 | G | A | 58 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(55): Show |
58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.414-5854G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121402 | |||||||
chr12:122121464 | C | A | 1 | a0002c0005t0009g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-5792C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121464 | |||||||
chr12:122121505 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.414-5751C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121505 | |||||||
chr12:122121506 | G | A | 1 | a0002c0004t0067g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-5750G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121506 | |||||||
chr12:122121629 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-5627A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121629 | |||||||
chr12:122121768 | C | A | 1 | a0002c0004t0052g0213 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414-5488C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121768 | |||||||
chr12:122122049 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5207A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122049 | |||||||
chr12:122122050 | C | CCTT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5204_414-5203i others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122050 | ||||||
chr12:122122115 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5141G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122115 | |||||||
chr12:122122212 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5044A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122212 | |||||||
chr12:122122280 | C | A | 1 | a0002c0002t0002g0225 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.414-4976C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122280 | |||||||
chr12:122122290 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-4966C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122290 | |||||||
chr12:122122340 | C | T | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-4916C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122340 | |||||||
chr12:122122368 | G | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.414-4888G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122368 | |||||||
chr12:122122370 | A | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-4886A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122370 | |||||||
chr12:122122514 | C | G | 1 | a0003c0018t0060g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.414-4742C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122514 | |||||||
chr12:122122516 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.414-4740A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122516 | |||||||
chr12:122122564 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0137 |
2 | NA18947.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.414-4692C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122564 | |||||||
chr12:122122565 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-4691A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122565 | |||||||
chr12:122122605 | G | T | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-4651G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122605 | |||||||
chr12:122122614 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.414-4642T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122614 | |||||||
chr12:122122635 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-4621A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122635 | |||||||
chr12:122122834 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-4422A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122834 | |||||||
chr12:122122860 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.414-4383dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122860 | ||||||
chr12:122122860 | CT | C | 9 | a0001c0003t0003g0282 a0001c0003t0003g0291 a0002c0002t0002g0200 others(6): Show |
9 | HG00323.hp1 HG01169.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-4383delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122860 | ||||||
chr12:122122884 | G | A | 2 | a0001c0008t0028g0016 a0001c0008t0028g0018 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.414-4372G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122884 | |||||||
chr12:122122940 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.414-4316G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122940 | |||||||
chr12:122122971 | C | T | 74 | a0001c0008t0055g0215 a0002c0002t0002g0005 a0002c0002t0002g0197 others(71): Show |
75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-4285C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122971 | |||||||
chr12:122123059 | G | A | 2 | a0006c0013t0002g0229 a0010c0021t0076g0012 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.414-4197G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123059 | |||||||
chr12:122123169 | T | G | 1 | a0001c0001t0006g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.414-4087T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123169 | |||||||
chr12:122123243 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0015g0145 |
2 | HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.414-4013G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123243 | |||||||
chr12:122123282 | C | A | 1 | a0002c0002t0037g0219 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414-3974C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123282 | |||||||
chr12:122123318 | C | T | 1 | a0002c0002t0039g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.414-3938C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123318 | |||||||
chr12:122123369 | C | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3887C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123369 | |||||||
chr12:122123404 | G | A | 37 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.414-3852G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123404 | |||||||
chr12:122123420 | C | T | 1 | a0002c0002t0012g0004 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.414-3836C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123420 | |||||||
chr12:122123517 | C | T | 93 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(90): Show |
94 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-3739C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123517 | |||||||
chr12:122123596 | G | A | 11 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(8): Show |
11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-3660G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123596 | |||||||
chr12:122123608 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3648G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123608 | |||||||
chr12:122123662 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.414-3594G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123662 | |||||||
chr12:122123955 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3301T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123955 | |||||||
chr12:122124089 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3167A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124089 | |||||||
chr12:122124111 | C | A | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.414-3145C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124111 | |||||||
chr12:122124173 | C | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0130 |
3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-3083C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124173 | |||||||
chr12:122124197 | CTCAGCTG others(10): Show |
C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3058_414-3042d others(19): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124197 | |||||||
chr12:122124203 | T | C | 94 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(91): Show |
95 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.414-3053T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124203 | |||||||
chr12:122124211 | T | TCCTCAGC others(27): Show |
1 | a0001c0008t0028g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414-3035_414-3002d others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124211 | ||||||
chr12:122124221 | TC | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3029delC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124221 | ||||||
chr12:122124228 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3028A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124228 | |||||||
chr12:122124229 | C | T | 1 | a0002c0002t0002g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-3027C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124229 | |||||||
chr12:122124233 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3023C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124233 | |||||||
chr12:122124245 | A | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3011A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124245 | |||||||
chr12:122124254 | G | GC | 39 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0113 others(36): Show |
39 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.414-2995dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124254 | ||||||
chr12:122124309 | CCCCTCCT others(92): Show |
C | 1 | a0002c0002t0002g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-2943_414-2845d others(101): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124309 | ||||||
chr12:122124326 | CCCCACCC others(75): Show |
C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0113 a0001c0001t0001g0138 others(2): Show |
5 | HG00738.hp2 HG01934.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-2926_414-2845d others(84): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124326 | ||||||
chr12:122124330 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.414-2926A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124330 | |||||||
chr12:122124331 | CCCTCAGC others(9): Show |
C | 3 | a0002c0002t0002g0199 a0002c0002t0016g0177 a0002c0002t0016g0186 |
3 | HG01070.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.414-2909_414-2894d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | ||||||
chr12:122124331 | CCCTCAGC others(76): Show |
C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-2892_414-2810d others(85): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | ||||||
chr12:122124331 | CCCTCAGC others(92): Show |
C | 1 | a0004c0007t0034g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.414-2909_414-2811d others(101): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | ||||||
chr12:122124359 | CCCCGTCC others(42): Show |
C | 1 | a0001c0001t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414-2893_414-2845d others(51): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124359 | ||||||
chr12:122124380 | A | ACCTCAGC others(9): Show |
1 | a0002c0002t0054g0300 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.414-2867_414-2866i others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124380 | ||||||
chr12:122124389 | G | GC | 20 | a0001c0003t0003g0298 a0001c0008t0047g0289 a0002c0002t0002g0198 others(17): Show |
20 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-2860dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124389 | ||||||
chr12:122124413 | C | CCACCTCA others(29): Show |
1 | a0002c0002t0002g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.414-2843_414-2842i others(38): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124413 | |||||||
chr12:122124413 | C | G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG00738.hp2 HG01934.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2843C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124413 | |||||||
chr12:122124414 | A | ACCTCAGC others(28): Show |
1 | a0002c0004t0005g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.414-2811_414-2810i others(37): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | ||||||
chr12:122124414 | A | ACCTCAGC others(27): Show |
83 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(80): Show |
84 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-2811_414-2810i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | ||||||
chr12:122124414 | A | ATCTCAGC others(27): Show |
8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-2842_414-2841i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124414 | |||||||
chr12:122124414 | A | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0089 a0001c0001t0001g0113 others(5): Show |
8 | HG00738.hp2 HG01934.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2842A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124414 | |||||||
chr12:122124414 | ACCTCAGC others(9): Show |
A | 10 | a0001c0003t0003g0302 a0001c0003t0003g0303 a0001c0003t0003g0318 others(7): Show |
10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-2826_414-2811d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | ||||||
chr12:122124531 | C | T | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-2725C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124531 | |||||||
chr12:122124584 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.414-2672C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124584 | |||||||
chr12:122124656 | G | A | 1 | a0002c0004t0005g0009 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-2600G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124656 | |||||||
chr12:122124658 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2598C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124658 | |||||||
chr12:122124736 | T | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2520T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124736 | |||||||
chr12:122124886 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.414-2370G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124886 | |||||||
chr12:122124957 | A | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-2299A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124957 | |||||||
chr12:122125035 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.414-2221G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125035 | |||||||
chr12:122125237 | C | T | 7 | a0002c0002t0026g0187 a0002c0002t0026g0202 a0002c0002t0044g0203 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2019C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125237 | |||||||
chr12:122125331 | C | CA | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.414-1911dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | ||||||
chr12:122125331 | C | CAA | 11 | a0001c0001t0001g0094 a0001c0001t0007g0078 a0004c0007t0019g0335 others(8): Show |
11 | HG01099.hp2 HG01192.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1912_414-1911d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | ||||||
chr12:122125331 | CA | C | 67 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(64): Show |
67 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.414-1911delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | ||||||
chr12:122125418 | T | G | 1 | a0001c0003t0003g0283 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.414-1838T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125418 | |||||||
chr12:122125442 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-1814A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125442 | |||||||
chr12:122125472 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-1784C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125472 | |||||||
chr12:122125567 | A | G | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-1689A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125567 | |||||||
chr12:122125581 | C | T | 11 | a0002c0002t0005g0027 a0002c0002t0005g0041 a0002c0002t0005g0043 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1675C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125581 | |||||||
chr12:122125598 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-1658C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125598 | |||||||
chr12:122125630 | G | A | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.414-1626G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125630 | |||||||
chr12:122125645 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414-1611G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125645 | |||||||
chr12:122125738 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-1518G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125738 | |||||||
chr12:122125942 | G | C | 1 | a0001c0003t0003g0283 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.414-1314G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125942 | |||||||
chr12:122126001 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414-1255G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126001 | |||||||
chr12:122126046 | A | T | 74 | a0001c0008t0055g0215 a0002c0002t0002g0005 a0002c0002t0002g0197 others(71): Show |
75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-1210A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126046 | |||||||
chr12:122126059 | C | T | 2 | a0002c0002t0021g0181 a0002c0004t0021g0182 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-1197C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126059 | |||||||
chr12:122126103 | C | T | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1153C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126103 | |||||||
chr12:122126104 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0155 others(1): Show |
4 | HG01192.hp1 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-1152C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126104 | |||||||
chr12:122126105 | A | T | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1151A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126105 | |||||||
chr12:122126116 | A | T | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1140A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126116 | |||||||
chr12:122126117 | G | C | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1139G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126117 | |||||||
chr12:122126119 | A | G | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1137A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126119 | |||||||
chr12:122126136 | C | T | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1120C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126136 | |||||||
chr12:122126138 | A | T | 1 | a0013c0025t0025g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1118A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126138 | |||||||
chr12:122126362 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-894G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126362 | |||||||
chr12:122126376 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0130 |
3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-880G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126376 | |||||||
chr12:122126457 | A | T | 74 | a0001c0008t0055g0215 a0002c0002t0002g0005 a0002c0002t0002g0197 others(71): Show |
75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-799A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126457 | |||||||
chr12:122126552 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-704C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126552 | |||||||
chr12:122126553 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-703A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126553 | |||||||
chr12:122126603 | G | A | 4 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-653G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126603 | |||||||
chr12:122126653 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-603G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126653 | |||||||
chr12:122127053 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-203C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127053 | |||||||
chr12:122127055 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-201C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127055 | |||||||
chr12:122127073 | A | C | 1 | a0001c0001t0015g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.414-183A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127073 | |||||||
chr12:122127073 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-183A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127073 | |||||||
chr12:122127094 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-162C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127094 | |||||||
chr12:122127138 | G | A | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-118G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127138 | |||||||
chr12:122127385 | G | A | 1 | a0001c0001t0008g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.520+23G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127385 | |||||||
chr12:122127531 | A | T | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+169A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127531 | |||||||
chr12:122127599 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.520+237T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127599 | |||||||
chr12:122127778 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.521-105G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127778 | |||||||
chr12:122127803 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.521-80G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127803 | |||||||
chr12:122127981 | G | A | 1 | a0001c0001t0033g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.606+13G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122127981 | |||||||
chr12:122128051 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.606+83T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128051 | |||||||
chr12:122128078 | C | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.606+110C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128078 | |||||||
chr12:122128088 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.606+120G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128088 | |||||||
chr12:122128201 | T | A | 2 | a0001c0001t0011g0052 a0001c0001t0011g0054 |
2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.606+233T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128201 | |||||||
chr12:122128453 | T | C | 74 | a0001c0008t0055g0215 a0002c0002t0002g0005 a0002c0002t0002g0197 others(71): Show |
75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.606+485T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128453 | |||||||
chr12:122128645 | C | G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-492C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128645 | |||||||
chr12:122128685 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.607-452G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128685 | |||||||
chr12:122128693 | C | T | 2 | a0002c0004t0024g0184 a0002c0004t0024g0185 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.607-444C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128693 | |||||||
chr12:122128731 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.607-406C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128731 | |||||||
chr12:122128765 | C | A | 19 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(16): Show |
19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.607-372C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128765 | |||||||
chr12:122128943 | C | T | 1 | a0002c0002t0040g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.607-194C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128943 | |||||||
chr12:122128974 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0042g0049 a0001c0001t0043g0050 |
3 | NA18982.hp2 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.607-163T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128974 | |||||||
chr12:122128993 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.607-144T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128993 | |||||||
chr12:122129006 | T | C | 1 | a0001c0001t0042g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.607-131T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122129006 | |||||||
chr12:122129052 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.607-85A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122129052 | |||||||
chr12:122129341 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.696+115G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129341 | |||||||
chr12:122129346 | G | A | 1 | a0002c0002t0005g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.696+120G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129346 | |||||||
chr12:122129396 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0015g0175 |
3 | HG01257.hp2 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.696+170C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129396 | |||||||
chr12:122129398 | C | T | 2 | a0002c0002t0002g0277 a0002c0002t0002g0278 |
2 | NA18947.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.696+172C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129398 | |||||||
chr12:122129417 | C | G | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-171C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129417 | |||||||
chr12:122129513 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(152): Show |
159 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.697-75G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129513 | |||||||
chr12:122129662 | CT | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+36delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 122129662 | ||||||
chr12:122129671 | G | C | 1 | a0002c0002t0039g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.738+42G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129671 | |||||||
chr12:122129840 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(162): Show |
169 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.739-101T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129840 | |||||||
chr12:122129889 | C | T | 6 | a0002c0004t0005g0045 a0002c0004t0005g0046 a0002c0004t0005g0048 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-52C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129889 | |||||||
chr12:122130218 | G | C | 1 | a0002c0004t0053g0190 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.910+106G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130218 | |||||||
chr12:122130223 | G | A | 5 | a0001c0001t0018g0082 a0001c0001t0018g0083 a0001c0001t0018g0104 others(2): Show |
5 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+111G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130223 | |||||||
chr12:122130239 | T | G | 4 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.910+127T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130239 | |||||||
chr12:122130311 | T | C | 6 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(3): Show |
6 | HG01099.hp2 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+199T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130311 | |||||||
chr12:122130362 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.910+250A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130362 | |||||||
chr12:122130441 | G | A | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+329G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130441 | |||||||
chr12:122130452 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.910+340G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130452 | |||||||
chr12:122130486 | G | A | 70 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.911-358G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130486 | |||||||
chr12:122130496 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.911-348G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130496 | |||||||
chr12:122130591 | T | C | 1 | a0001c0001t0057g0344 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.911-253T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130591 | |||||||
chr12:122130728 | C | A | 1 | a0002c0011t0036g0264 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.911-116C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130728 | |||||||
chr12:122130968 | C | G | 209 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(206): Show |
210 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1000+35C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122130968 | |||||||
chr12:122131044 | G | A | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1000+111G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131044 | |||||||
chr12:122131186 | A | G | 1 | a0002c0002t0054g0300 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1000+253A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131186 | |||||||
chr12:122131394 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0015g0175 |
3 | HG01257.hp2 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1000+461C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131394 | |||||||
chr12:122131417 | G | T | 175 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(172): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1000+484G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131417 | |||||||
chr12:122131441 | C | CT | 99 | a0001c0001t0001g0074 a0001c0001t0001g0089 a0001c0001t0001g0102 others(96): Show |
99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1000+533dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | ||||||
chr12:122131441 | C | CTT | 72 | a0001c0003t0003g0282 a0001c0003t0003g0283 a0001c0003t0003g0305 others(69): Show |
73 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1000+532_1000+533d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | ||||||
chr12:122131441 | C | CTTT | 9 | a0002c0002t0002g0245 a0002c0002t0002g0249 a0002c0002t0002g0251 others(6): Show |
9 | HG01891.hp1 HG02027.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000+531_1000+533d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | ||||||
chr12:122131441 | C | CTTTTT | 7 | a0002c0002t0010g0022 a0002c0002t0010g0023 a0002c0002t0010g0024 others(4): Show |
7 | HG00621.hp2 HG03704.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+529_1000+533d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | ||||||
chr12:122131441 | CT | C | 19 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0130 others(16): Show |
19 | HG01168.hp2 HG01256.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1000+533delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | ||||||
chr12:122131552 | C | T | 176 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(173): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1000+619C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131552 | |||||||
chr12:122131693 | T | C | 88 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(85): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1001-599T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131693 | |||||||
chr12:122131739 | G | A | 175 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(172): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1001-553G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131739 | |||||||
chr12:122131816 | C | T | 4 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-476C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131816 | |||||||
chr12:122131912 | C | CT | 21 | a0001c0001t0001g0073 a0001c0001t0001g0112 a0001c0001t0001g0149 others(18): Show |
21 | HG00140.hp1 HG00621.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-351dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CT | C | 21 | a0001c0001t0001g0062 a0001c0001t0001g0084 a0001c0001t0001g0086 others(18): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-351delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTT | C | 18 | a0001c0001t0001g0102 a0001c0001t0033g0163 a0002c0002t0005g0027 others(15): Show |
18 | HG01256.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1001-352_1001-351d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTT | C | 14 | a0001c0003t0003g0282 a0001c0003t0003g0283 a0001c0003t0003g0298 others(11): Show |
14 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-353_1001-351d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTTT | C | 83 | a0001c0003t0003g0006 a0001c0003t0003g0284 a0001c0003t0003g0286 others(80): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1001-354_1001-351d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTTTT | C | 78 | a0001c0003t0003g0324 a0001c0008t0028g0016 a0001c0008t0028g0018 others(75): Show |
79 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1001-355_1001-351d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTTTTTT others(1): Show |
C | 6 | a0004c0007t0034g0331 a0004c0007t0034g0332 a0004c0007t0074g0334 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-358_1001-351d others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-359_1001-351d others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122131912 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0010g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1001-365_1001-351d others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | ||||||
chr12:122132211 | C | A | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1001-81C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132211 | |||||||
chr12:122132212 | G | A | 176 | a0001c0001t0057g0344 a0001c0003t0003g0006 a0001c0003t0003g0282 others(173): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1001-80G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132212 | |||||||
chr12:122132219 | G | A | 176 | a0001c0001t0057g0344 a0001c0003t0003g0006 a0001c0003t0003g0282 others(173): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1001-73G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132219 | |||||||
chr12:122132411 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1092+28G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132411 | |||||||
chr12:122132729 | C | T | 8 | a0002c0002t0010g0019 a0002c0002t0010g0022 a0002c0002t0010g0023 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092+346C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132729 | |||||||
chr12:122132768 | TG | T | 175 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(172): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1092+389delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr12 | 122132768 | ||||||
chr12:122132843 | A | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1092+460A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132843 | |||||||
chr12:122132871 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1093-477C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132871 | |||||||
chr12:122132987 | C | T | 1 | a0001c0001t0022g0090 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1093-361C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132987 | |||||||
chr12:122133011 | C | G | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-337C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122133011 | |||||||
chr12:122134025 | C | T | 1 | a0001c0001t0008g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1732+38C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134025 | |||||||
chr12:122134205 | G | GT | 95 | a0001c0001t0001g0158 a0001c0001t0001g0188 a0001c0001t0007g0088 others(92): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1732+231dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | ||||||
chr12:122134205 | G | GTT | 36 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(33): Show |
36 | HG01099.hp2 HG01123.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1732+230_1732+231d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | ||||||
chr12:122134205 | G | GTTT | 17 | a0002c0002t0005g0027 a0002c0002t0005g0043 a0002c0004t0005g0007 others(14): Show |
17 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1732+229_1732+231d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | ||||||
chr12:122134264 | G | A | 7 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1732+277G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134264 | |||||||
chr12:122134277 | C | T | 1 | a0001c0001t0043g0050 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1732+290C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134277 | |||||||
chr12:122134304 | CCTT | C | 3 | a0002c0002t0026g0187 a0002c0002t0026g0202 a0002c0002t0044g0203 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1732+319_1732+321d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134304 | ||||||
chr12:122134419 | T | C | 175 | a0001c0001t0015g0143 a0001c0003t0003g0006 a0001c0003t0003g0282 others(172): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1732+432T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134419 | |||||||
chr12:122134428 | G | A | 2 | a0002c0004t0003g0216 a0002c0004t0003g0217 |
2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1732+441G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134428 | |||||||
chr12:122134445 | C | CA | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1732+460dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134445 | ||||||
chr12:122134677 | C | CT | 92 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1733-533dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134677 | ||||||
chr12:122134677 | CT | C | 22 | a0001c0001t0001g0084 a0001c0001t0008g0165 a0001c0001t0032g0111 others(19): Show |
22 | HG01069.hp2 HG01243.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.1733-533delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134677 | ||||||
chr12:122134714 | G | T | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1733-510G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134714 | |||||||
chr12:122134767 | C | T | 4 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0027g0014 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733-457C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134767 | |||||||
chr12:122134850 | C | T | 202 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(199): Show |
203 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1733-374C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134850 | |||||||
chr12:122134939 | G | T | 3 | a0001c0003t0003g0312 a0001c0003t0003g0313 a0001c0003t0003g0314 |
3 | HG00741.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1733-285G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134939 | |||||||
chr12:122134981 | CT | C | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1733-235delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134981 | ||||||
chr12:122135159 | C | T | 9 | a0004c0007t0019g0335 a0004c0007t0034g0331 a0004c0007t0034g0332 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733-65C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122135159 | |||||||
chr12:122135683 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+17C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135683 | |||||||
chr12:122135700 | C | T | 1 | a0002c0009t0069g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2032+34C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135700 | |||||||
chr12:122135816 | C | T | 1 | a0002c0004t0067g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2032+150C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135816 | |||||||
chr12:122135834 | G | T | 1 | a0002c0002t0002g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2032+168G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135834 | |||||||
chr12:122135919 | C | T | 1 | a0002c0002t0002g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2032+253C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135919 | |||||||
chr12:122136142 | A | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032+476A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136142 | |||||||
chr12:122136178 | A | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG02683.hp2 HG02738.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2032+512A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136178 | |||||||
chr12:122136217 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+551G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136217 | |||||||
chr12:122136387 | T | TA | 6 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2032+721_2032+722i others(3): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136387 | |||||||
chr12:122136411 | G | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+745G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136411 | |||||||
chr12:122136457 | TGC | T | 8 | a0001c0008t0028g0018 a0001c0008t0055g0215 a0002c0002t0012g0004 others(5): Show |
9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+792_2032+793d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | |||||||
chr12:122136457 | TGCA | T | 4 | a0001c0003t0003g0311 a0001c0003t0003g0314 a0002c0004t0004g0195 others(1): Show |
4 | HG00741.hp2 HG03579.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+792_2032+794d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | |||||||
chr12:122136457 | TGCAA | T | 80 | a0001c0003t0003g0006 a0001c0003t0003g0283 a0001c0003t0003g0284 others(77): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2032+792_2032+795d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | |||||||
chr12:122136458 | G | A | 80 | a0001c0008t0028g0016 a0002c0002t0002g0005 a0002c0002t0002g0197 others(77): Show |
80 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2032+792G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136458 | |||||||
chr12:122136459 | C | CA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0120 others(25): Show |
29 | HG00544.hp2 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2032+816dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | ||||||
chr12:122136459 | C | CAAAAAA | 22 | a0002c0002t0005g0041 a0002c0002t0005g0043 a0002c0004t0005g0007 others(19): Show |
22 | HG01099.hp2 HG01884.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.2032+811_2032+816d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | ||||||
chr12:122136459 | CA | C | 18 | a0001c0001t0001g0115 a0001c0001t0015g0143 a0001c0001t0033g0163 others(15): Show |
18 | HG00621.hp2 HG02027.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2032+816delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | ||||||
chr12:122136461 | A | C | 8 | a0001c0008t0028g0018 a0001c0008t0055g0215 a0002c0002t0012g0004 others(5): Show |
9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+795A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136461 | |||||||
chr12:122136461 | A | T | 1 | a0015c0015t0003g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2032+795A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136461 | |||||||
chr12:122136462 | A | C | 4 | a0001c0003t0003g0311 a0001c0003t0003g0314 a0002c0004t0004g0195 others(1): Show |
4 | HG00741.hp2 HG03579.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+796A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136462 | |||||||
chr12:122136463 | A | C | 81 | a0001c0003t0003g0006 a0001c0003t0003g0283 a0001c0003t0003g0284 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2032+797A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136463 | |||||||
chr12:122136464 | A | C | 1 | a0001c0003t0003g0282 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2032+798A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136464 | |||||||
chr12:122136534 | T | C | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+868T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136534 | |||||||
chr12:122136841 | G | A | 13 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(10): Show |
13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033-628G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136841 | |||||||
chr12:122136868 | C | T | 1 | a0006c0013t0002g0229 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2033-601C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136868 | |||||||
chr12:122137116 | A | G | 4 | a0002c0004t0005g0045 a0002c0004t0005g0048 a0002c0004t0065g0047 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033-353A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137116 | |||||||
chr12:122137145 | T | G | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2033-324T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137145 | |||||||
chr12:122137187 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2033-282C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137187 | |||||||
chr12:122137217 | T | G | 1 | a0015c0015t0003g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-252T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137217 | |||||||
chr12:122137219 | G | A | 1 | a0015c0015t0003g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-250G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137219 | |||||||
chr12:122137441 | G | A | 5 | a0001c0008t0055g0215 a0002c0002t0012g0004 a0002c0002t0012g0210 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2033-28G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137441 | |||||||
chr12:122137444 | C | A | 1 | a0015c0015t0003g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-25C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137444 | |||||||
chr12:122137660 | CT | C | 177 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0001c0003t0003g0006 others(174): Show |
178 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2154+72delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 122137660 | ||||||
chr12:122137675 | G | A | 2 | a0001c0001t0033g0163 a0001c0001t0033g0164 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2154+85G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137675 | |||||||
chr12:122137836 | G | A | 1 | a0002c0002t0021g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2154+246G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137836 | |||||||
chr12:122137968 | C | G | 1 | a0002c0002t0026g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2155-226C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137968 | |||||||
chr12:122138090 | C | T | 1 | a0002c0002t0002g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2155-104C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122138090 | |||||||
chr12:122138620 | T | TGG | 13 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0002c0002t0010g0019 others(10): Show |
13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2384+71_2384+72dup others(2): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 122138620 | ||||||
chr12:122138735 | G | A | 1 | a0001c0001t0015g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2385-80G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/16 | chr12 | 122138735 | |||||||
chr12:122139008 | T | G | 1 | a0002c0002t0002g0266 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2508+70T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139008 | |||||||
chr12:122139048 | A | G | 88 | a0001c0008t0028g0016 a0001c0008t0028g0018 a0001c0008t0055g0215 others(85): Show |
89 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.2508+110A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139048 | |||||||
chr12:122139076 | C | T | 1 | a0011c0014t0019g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2508+138C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139076 | |||||||
chr12:122139387 | A | G | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2508+449A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139387 | |||||||
chr12:122139451 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2508+513G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139451 | |||||||
chr12:122139505 | G | C | 1 | a0014c0022t0023g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2508+567G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139505 | |||||||
chr12:122139617 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2508+679C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139617 | |||||||
chr12:122139657 | A | G | 2 | a0005c0012t0072g0160 a0005c0012t0073g0159 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2508+719A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139657 | |||||||
chr12:122139705 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2508+767C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139705 | |||||||
chr12:122139803 | G | A | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2508+865G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139803 | |||||||
chr12:122139834 | C | T | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2508+896C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139834 | |||||||
chr12:122140009 | A | G | 1 | a0001c0001t0029g0343 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2509-945A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140009 | |||||||
chr12:122140087 | G | A | 1 | a0001c0003t0003g0309 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2509-867G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140087 | |||||||
chr12:122140462 | A | G | 1 | a0001c0001t0013g0345 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2509-492A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140462 | |||||||
chr12:122140550 | C | T | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2509-404C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140550 | |||||||
chr12:122140584 | G | A | 33 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(30): Show |
33 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2509-370G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140584 | |||||||
chr12:122140662 | C | T | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2509-292C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140662 | |||||||
chr12:122140665 | A | G | 207 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(204): Show |
208 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2509-289A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140665 | |||||||
chr12:122140895 | C | T | 1 | a0002c0002t0002g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2509-59C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140895 | |||||||
chr12:122140921 | C | T | 1 | a0001c0001t0007g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2509-33C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140921 | |||||||
chr12:122141199 | C | A | 3 | a0002c0005t0009g0233 a0002c0005t0009g0236 a0002c0005t0009g0239 |
3 | HG01109.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2638+116C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141199 | |||||||
chr12:122141208 | A | G | 71 | a0002c0002t0002g0005 a0002c0002t0002g0197 a0002c0002t0002g0198 others(68): Show |
71 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2638+125A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141208 | |||||||
chr12:122141227 | T | G | 174 | a0001c0003t0003g0006 a0001c0003t0003g0282 a0001c0003t0003g0283 others(171): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2638+144T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141227 | |||||||
chr12:122141417 | G | A | 6 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2639-274G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141417 | |||||||
chr12:122141445 | A | G | 207 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 others(204): Show |
208 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2639-246A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141445 | |||||||
chr12:122141480 | G | A | 1 | a0010c0021t0076g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2639-211G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141480 | |||||||
chr12:122141503 | C | A | 2 | a0002c0002t0021g0181 a0002c0004t0021g0182 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2639-188C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141503 | |||||||
chr12:122141568 | C | T | 3 | a0001c0001t0033g0163 a0001c0001t0033g0164 a0002c0009t0069g0035 |
3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2639-123C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141568 |