Item | Value |
---|---|
geneid | 6433 |
ensemblid | ENSG00000061936.10 |
hgncid | 10790 |
symbol | SFSWAP |
name | splicing factor SWAP |
refseq_nuc | NM_004592.4 |
refseq_prot | NP_004583.2 |
ensembl_nuc | ENST00000261674.9 |
ensembl_prot | ENSP00000261674.4 |
mane_status | MANE Select |
chr | chr12 |
start | 131711090 |
end | 131799738 |
strand | + |
ver | v1.2 |
region | chr12:131711090-131799738 |
region5000 | chr12:131706090-131804738 |
regionname0 | SFSWAP_chr12_131711090_131799738 |
regionname5000 | SFSWAP_chr12_131706090_131804738 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 951 | 284 | 69 | 69 | 104 | 10 | 31 | 75 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0002 | 1/0 | 951 | 18 | 11 | 1 | 1 | 2 | 2 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0003 | 0/0 | 951 | 4 | 1 | 1 | 2 | 0 | 0 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0004 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0005 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0006 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0007 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0008 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0009 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0010 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0011 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0012 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0013 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
a0014 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | MYGAS others(946): Show |
chr12 | 131706090 | 131804738 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2853 | 241 | 52 | 51 | 103 | 8 | 26 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0002 | 0/0 | 2853 | 19 | 1 | 13 | 0 | 2 | 3 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0004 | 0/0 | 2853 | 6 | 6 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0006 | 0/0 | 2853 | 3 | 3 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0007 | 0/0 | 2853 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0008 | 0/0 | 2853 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0010 | 0/0 | 2853 | 2 | 0 | 1 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0011 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0012 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0015 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0018 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0019 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0029 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0001c0031 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0002c0003 | 0/0 | 2853 | 14 | 10 | 1 | 1 | 2 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0002c0025 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0002c0026 | 1/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0002c0027 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0002c0028 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0003c0005 | 0/0 | 2854 | 4 | 1 | 1 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2849): Show |
chr12 | 131706090 | 131804738 | ||
a0004c0009 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0005c0016 | 0/0 | 2853 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0006c0020 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0007c0021 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0008c0023 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2849): Show |
chr12 | 131706090 | 131804738 | ||
a0009c0022 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0010c0014 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0011c0017 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0012c0024 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0013c0013 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 | ||
a0014c0030 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATGTA others(2848): Show |
chr12 | 131706090 | 131804738 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3246 | 196 | 26 | 45 | 98 | 8 | 18 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0001t0002 | 0/0 | 3246 | 33 | 15 | 5 | 5 | 0 | 8 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0001t0003 | 0/0 | 3246 | 10 | 10 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0001t0004 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0001t0005 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0002t0001 | 0/0 | 3246 | 19 | 1 | 13 | 0 | 2 | 3 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0004t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0004t0002 | 0/0 | 3246 | 5 | 5 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0006t0001 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0007t0001 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0008t0001 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0010t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0010t0004 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0011t0002 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0012t0001 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0015t0002 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0018t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0019t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0029t0002 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0001c0031t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0003t0003 | 0/0 | 3246 | 12 | 10 | 1 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0003t0004 | 0/0 | 3246 | 2 | 0 | 0 | 1 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0025t0004 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0026t0004 | 1/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0027t0003 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0002c0028t0004 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0003c0005t0001 | 0/0 | 3247 | 4 | 1 | 1 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3242): Show |
chr12 | 131706090 | 131804738 |
a0004c0009t0001 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0005c0016t0001 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0006c0020t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0007c0021t0003 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0008c0023t0001 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3242): Show |
chr12 | 131706090 | 131804738 |
a0009c0022t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0010c0014t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0011c0017t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0012c0024t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0013c0013t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
a0014c0030t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | ATTTT others(3241): Show |
chr12 | 131706090 | 131804738 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0007t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0007t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0008t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0010t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0010t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0011t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0011t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0012t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0012t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0015t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0018t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0019t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0029t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0031t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0025t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0026t0004g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0027t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0028t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0004c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0004c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0005c0016t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0006c0020t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0007c0021t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0008c0023t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0009c0022t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0010c0014t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0011c0017t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0012c0024t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0013c0013t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0014c0030t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0292 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0286 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00733 | hp2 | a0001 | c0008 | t0001 | g0235 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01168 | hp2 | a0001 | c0007 | t0001 | g0296 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01169 | hp1 | a0001 | c0007 | t0001 | g0284 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01175 | hp1 | a0001 | c0008 | t0001 | g0236 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01175 | hp2 | a0003 | c0005 | t0001 | g0121 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01261 | hp1 | a0001 | c0010 | t0004 | g0023 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01891 | hp1 | a0004 | c0009 | t0001 | g0052 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01891 | hp2 | a0001 | c0004 | t0002 | g0011 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01934 | hp2 | a0002 | c0003 | t0003 | g0033 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01978 | hp2 | a0005 | c0016 | t0001 | g0214 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02071 | hp1 | a0006 | c0020 | t0001 | g0280 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02129 | hp2 | a0001 | c0010 | t0001 | g0240 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0030 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02257 | hp1 | a0003 | c0005 | t0001 | g0120 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02257 | hp2 | a0002 | c0027 | t0003 | g0035 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02258 | hp2 | a0004 | c0009 | t0001 | g0053 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02451 | hp1 | a0001 | c0015 | t0002 | g0008 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02451 | hp2 | a0007 | c0021 | t0003 | g0020 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02572 | hp2 | a0002 | c0003 | t0003 | g0040 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02717 | hp2 | a0001 | c0011 | t0002 | g0080 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02922 | hp1 | a0001 | c0006 | t0001 | g0015 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02965 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02976 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03017 | hp2 | a0002 | c0028 | t0004 | g0309 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03041 | hp1 | a0001 | c0011 | t0002 | g0081 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0306 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03098 | hp2 | a0001 | c0012 | t0001 | g0044 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03139 | hp2 | a0001 | c0012 | t0001 | g0045 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0307 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03225 | hp2 | a0001 | c0018 | t0001 | g0016 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03239 | hp2 | a0009 | c0022 | t0001 | g0125 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03453 | hp1 | a0001 | c0031 | t0001 | g0046 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03490 | hp1 | a0010 | c0014 | t0001 | g0272 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03540 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04199 | hp1 | a0002 | c0025 | t0004 | g0042 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04228 | hp1 | a0001 | c0029 | t0002 | g0059 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04228 | hp2 | a0001 | c0019 | t0001 | g0188 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18906 | hp1 | a0002 | c0003 | t0003 | g0027 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18962 | hp2 | a0012 | c0024 | t0001 | g0131 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18966 | hp1 | a0003 | c0005 | t0001 | g0251 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19009 | hp2 | a0013 | c0013 | t0001 | g0111 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19030 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0026 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19057 | hp1 | a0002 | c0003 | t0004 | g0022 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19072 | hp1 | a0003 | c0005 | t0001 | g0199 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ASW | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20752 | hp1 | a0002 | c0003 | t0003 | g0041 | EUR | TSI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20752 | hp2 | a0002 | c0003 | t0004 | g0024 | EUR | TSI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20905 | hp1 | a0014 | c0030 | t0001 | g0189 | SAS | GIH | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | GIH | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0285 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02109 | hp2 | a0002 | c0003 | t0003 | g0034 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02486 | hp2 | a0002 | c0003 | t0003 | g0043 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02559 | hp1 | a0008 | c0023 | t0001 | g0051 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0010 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG06807 | hp1 | a0011 | c0017 | t0001 | g0209 | AFR | USA | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0032 | AFR | USA | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0213 | REF | REF | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
homoSapiens | grch38p0 | a0002 | c0026 | t0004 | g0029 | REF | REF | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711375 | A | G | 1 | a0014 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.146A>G | p.Glu49Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 286/3246 | 146/2856 | 49/951 | chr12 | 131711375 | |||
chr12:131714138 | G | C | 1 | a0013 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.286G>C | p.Asp96His | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/18 | 426/3246 | 286/2856 | 96/951 | chr12 | 131714138 | |||
chr12:131719498 | G | A | 1 | a0010 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.565G>A | p.Val189Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/18 | 705/3246 | 565/2856 | 189/951 | chr12 | 131719498 | |||
chr12:131753245 | G | A | 1 | a0005 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1204G>A | p.Val402Met | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1344/3246 | 1204/2856 | 402/951 | chr12 | 131753245 | |||
chr12:131753303 | T | C | 13 | a0001 a0003 a0004 others(10): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
missense_variant | MODERATE | c.1262T>C | p.Leu421Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1402/3246 | 1262/2856 | 421/951 | chr12 | 131753303 | |||
chr12:131753306 | C | T | 1 | a0012 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.1265C>T | p.Pro422Leu | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1405/3246 | 1265/2856 | 422/951 | chr12 | 131753306 | |||
chr12:131755465 | G | A | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1534G>A | p.Gly512Ser | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/18 | 1674/3246 | 1534/2856 | 512/951 | chr12 | 131755465 | |||
chr12:131756537 | A | G | 2 | a0004 a0008 |
3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.1613A>G | p.Glu538Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/18 | 1753/3246 | 1613/2856 | 538/951 | chr12 | 131756537 | |||
chr12:131778324 | G | A | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2402G>A | p.Arg801Gln | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/18 | 2542/3246 | 2402/2856 | 801/951 | chr12 | 131778324 | |||
chr12:131797206 | C | CG | 2 | a0003 a0008 |
5 | HG01175.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
frameshift_variant | HIGH | c.2565dupG | p.Ser856fs | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2706/3246 | 2566/2856 | 856/951 | INFO_REALIGN_3_PRIME | chr12 | 131797206 | ||
chr12:131797317 | G | A | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2674G>A | p.Val892Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2814/3246 | 2674/2856 | 892/951 | chr12 | 131797317 | |||
chr12:131797354 | G | A | 1 | a0009 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2711G>A | p.Arg904His | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2851/3246 | 2711/2856 | 904/951 | chr12 | 131797354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711310 | C | T | 2 | a0001c0012 a0001c0031 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.81C>T | p.Gly27Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 221/3246 | 81/2856 | 27/951 | chr12 | 131711310 | |||
chr12:131719467 | C | T | 1 | a0001c0029 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.534C>T | p.Ala178Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/18 | 674/3246 | 534/2856 | 178/951 | chr12 | 131719467 | |||
chr12:131725413 | C | T | 1 | a0001c0011 | 2 | HG02717.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.615C>T | p.Thr205Thr | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/18 | 755/3246 | 615/2856 | 205/951 | chr12 | 131725413 | |||
chr12:131725518 | T | C | 2 | a0001c0004 a0001c0015 |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.720T>C | p.Phe240Phe | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/18 | 860/3246 | 720/2856 | 240/951 | chr12 | 131725518 | |||
chr12:131753202 | C | T | 1 | a0002c0028 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1161C>T | p.Ile387Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1301/3246 | 1161/2856 | 387/951 | chr12 | 131753202 | |||
chr12:131753205 | C | T | 2 | a0001c0002 a0001c0010 |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
synonymous_variant | LOW | c.1164C>T | p.Asp388Asp | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1304/3246 | 1164/2856 | 388/951 | chr12 | 131753205 | |||
chr12:131754407 | C | T | 1 | a0001c0006 | 3 | HG02922.hp1 HG03130.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/18 | 1502/3246 | 1362/2856 | 454/951 | chr12 | 131754407 | |||
chr12:131754443 | T | C | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1398T>C | p.Tyr466Tyr | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/18 | 1538/3246 | 1398/2856 | 466/951 | chr12 | 131754443 | |||
chr12:131755464 | G | T | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1533G>T | p.Gly511Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/18 | 1673/3246 | 1533/2856 | 511/951 | chr12 | 131755464 | |||
chr12:131756562 | C | T | 1 | a0002c0027 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1638C>T | p.Ala546Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/18 | 1778/3246 | 1638/2856 | 546/951 | chr12 | 131756562 | |||
chr12:131766167 | G | C | 3 | a0001c0002 a0001c0007 a0002c0025 |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
synonymous_variant | LOW | c.2001G>C | p.Leu667Leu | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/18 | 2141/3246 | 2001/2856 | 667/951 | chr12 | 131766167 | |||
chr12:131766227 | G | A | 2 | a0001c0006 a0001c0018 |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.2061G>A | p.Ala687Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/18 | 2201/3246 | 2061/2856 | 687/951 | chr12 | 131766227 | |||
chr12:131778169 | G | A | 1 | a0001c0019 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.2247G>A | p.Pro749Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/18 | 2387/3246 | 2247/2856 | 749/951 | chr12 | 131778169 | |||
chr12:131786568 | T | C | 28 | a0001c0001 a0001c0002 a0001c0004 others(25): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
synonymous_variant | LOW | c.2514T>C | p.Ser838Ser | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/18 | 2654/3246 | 2514/2856 | 838/951 | chr12 | 131786568 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711129 | A | C | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0002t0001 others(24): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
5_prime_UTR_variant | MODIFIER | c.-101A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 101 | chr12 | 131711129 | ||||||
chr12:131711129 | A | T | 1 | a0001c0001t0005 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 101 | chr12 | 131711129 | ||||||
chr12:131799508 | G | A | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0004t0002 others(6): Show |
66 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*20G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 18/18 | 20 | chr12 | 131799508 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711491 | C | T | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+44C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711491 | |||||||
chr12:131711712 | A | G | 1 | a0001c0001t0002g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+265A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711712 | |||||||
chr12:131711798 | C | T | 1 | a0002c0028t0004g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218+351C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711798 | |||||||
chr12:131712193 | T | A | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+746T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712193 | |||||||
chr12:131712284 | T | G | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218+837T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712284 | |||||||
chr12:131712751 | C | T | 1 | a0001c0001t0003g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218+1304C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712751 | |||||||
chr12:131712752 | A | G | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1305A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712752 | |||||||
chr12:131713002 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-1069T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131713002 | |||||||
chr12:131713966 | C | T | 1 | a0001c0001t0004g0305 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-105C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131713966 | |||||||
chr12:131714016 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-55G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131714016 | |||||||
chr12:131714561 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389-261A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/17 | chr12 | 131714561 | |||||||
chr12:131714762 | T | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.389-60T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/17 | chr12 | 131714762 | |||||||
chr12:131715372 | TG | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+421delG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 131715372 | ||||||
chr12:131715461 | C | G | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.520+508C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715461 | |||||||
chr12:131715579 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.520+626C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715579 | |||||||
chr12:131715582 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.520+629A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715582 | |||||||
chr12:131715597 | C | T | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520+644C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715597 | |||||||
chr12:131715615 | C | T | 2 | a0001c0001t0001g0279 a0006c0020t0001g0280 |
2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.520+662C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715615 | |||||||
chr12:131715617 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.520+664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715617 | |||||||
chr12:131715681 | A | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG00741.hp2 HG01167.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+728A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715681 | |||||||
chr12:131715749 | TTTACA | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(79): Show |
83 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.520+803_520+807del others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 131715749 | ||||||
chr12:131715897 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.520+944A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715897 | |||||||
chr12:131715945 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.520+992C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715945 | |||||||
chr12:131716360 | G | A | 2 | a0001c0001t0003g0018 a0001c0006t0001g0014 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+1407G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716360 | |||||||
chr12:131716571 | T | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520+1618T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716571 | |||||||
chr12:131716588 | C | T | 1 | a0010c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.520+1635C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716588 | |||||||
chr12:131717057 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | NA18942.hp1 NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.520+2104C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717057 | |||||||
chr12:131717177 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.520+2224G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717177 | |||||||
chr12:131717242 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.521-2212C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717242 | |||||||
chr12:131717416 | A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.521-2038A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717416 | |||||||
chr12:131717463 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.521-1991A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717463 | |||||||
chr12:131718117 | A | G | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.521-1337A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718117 | |||||||
chr12:131718264 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.521-1190T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718264 | |||||||
chr12:131718389 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.521-1065C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718389 | |||||||
chr12:131718599 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.521-855G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718599 | |||||||
chr12:131718688 | C | T | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-766C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718688 | |||||||
chr12:131718971 | A | G | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.521-483A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718971 | |||||||
chr12:131718986 | A | G | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.521-468A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718986 | |||||||
chr12:131719043 | T | G | 91 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0047 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.521-411T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719043 | |||||||
chr12:131719129 | C | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-325C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719129 | |||||||
chr12:131719130 | G | A | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.521-324G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719130 | |||||||
chr12:131719258 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.521-196C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719258 | |||||||
chr12:131719278 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.521-176A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719278 | |||||||
chr12:131719294 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.521-160G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719294 | |||||||
chr12:131719366 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.521-88A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719366 | |||||||
chr12:131719568 | C | T | 16 | a0001c0001t0001g0090 a0001c0001t0002g0084 a0001c0001t0002g0085 others(13): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+29C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719568 | |||||||
chr12:131719663 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.606+124G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719663 | |||||||
chr12:131719843 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.606+304G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719843 | |||||||
chr12:131719949 | T | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.606+410T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719949 | |||||||
chr12:131720126 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.606+587A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720126 | |||||||
chr12:131720441 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.606+902G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720441 | |||||||
chr12:131720563 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(170): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.606+1024A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720563 | |||||||
chr12:131720585 | C | G | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.606+1046C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720585 | |||||||
chr12:131720589 | A | G | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.606+1050A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720589 | |||||||
chr12:131720984 | G | A | 1 | a0007c0021t0003g0020 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1445G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720984 | |||||||
chr12:131721598 | A | T | 19 | a0001c0001t0001g0090 a0001c0001t0002g0082 a0001c0001t0002g0084 others(16): Show |
19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.606+2059A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721598 | |||||||
chr12:131721599 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.606+2060T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721599 | |||||||
chr12:131721731 | G | C | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+2192G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721731 | |||||||
chr12:131721765 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.606+2226G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721765 | |||||||
chr12:131722044 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.606+2505T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722044 | |||||||
chr12:131722396 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.606+2857T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722396 | |||||||
chr12:131722434 | G | A | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.606+2895G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722434 | |||||||
chr12:131722590 | A | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.607-2815A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722590 | |||||||
chr12:131722624 | C | A | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.607-2781C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722624 | |||||||
chr12:131722854 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.607-2551C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722854 | |||||||
chr12:131722897 | T | C | 1 | a0006c0020t0001g0280 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.607-2508T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722897 | |||||||
chr12:131722917 | C | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-2488C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722917 | |||||||
chr12:131722989 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.607-2416C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722989 | |||||||
chr12:131723104 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp2 HG02148.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.607-2301T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723104 | |||||||
chr12:131723135 | T | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0002g0050 |
3 | HG01258.hp1 HG02818.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.607-2270T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723135 | |||||||
chr12:131723146 | TTCA | T | 3 | a0004c0009t0001g0052 a0004c0009t0001g0053 a0008c0023t0001g0051 |
3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.607-2254_607-2252d others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 131723146 | ||||||
chr12:131723279 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.607-2126C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723279 | |||||||
chr12:131723557 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.607-1848G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723557 | |||||||
chr12:131724273 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.607-1132G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131724273 | |||||||
chr12:131724972 | C | A | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-433C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131724972 | |||||||
chr12:131725110 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.607-295A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725110 | |||||||
chr12:131725236 | T | A | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-169T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725236 | |||||||
chr12:131725294 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.607-111A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725294 | |||||||
chr12:131725381 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.607-24G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725381 | |||||||
chr12:131725387 | ATG | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.607-12_607-11delGT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 131725387 | ||||||
chr12:131725684 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
6 | HG02040.hp2 HG03834.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+54G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131725684 | |||||||
chr12:131725924 | G | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | NA18960.hp1 NA19084.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.832+294G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131725924 | |||||||
chr12:131726078 | G | T | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.832+448G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726078 | |||||||
chr12:131726175 | T | TAC | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.832+559_832+560dup others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726175 | ||||||
chr12:131726177 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.832+547C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726177 | |||||||
chr12:131726202 | AT | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.832+585delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726202 | ||||||
chr12:131726223 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.832+593G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726223 | |||||||
chr12:131726224 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.832+594A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726224 | |||||||
chr12:131726257 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.832+627G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726257 | |||||||
chr12:131726356 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0079 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.833-584C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726356 | |||||||
chr12:131726420 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-520G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726420 | |||||||
chr12:131726475 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-465G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726475 | |||||||
chr12:131726671 | G | GA | 10 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-261dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726671 | ||||||
chr12:131726697 | C | T | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.833-243C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726697 | |||||||
chr12:131727347 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.945+295C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727347 | |||||||
chr12:131727466 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
22 | HG00558.hp2 HG02015.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.945+414C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727466 | |||||||
chr12:131727553 | G | T | 5 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+501G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727553 | |||||||
chr12:131727705 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.946-588A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727705 | |||||||
chr12:131727978 | A | G | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.946-315A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727978 | |||||||
chr12:131728271 | G | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.946-22G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131728271 | |||||||
chr12:131728563 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
52 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1081+135G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728563 | |||||||
chr12:131728669 | G | A | 1 | a0001c0002t0001g0285 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1081+241G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728669 | |||||||
chr12:131728816 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0002c0003t0003g0043 |
3 | HG01243.hp1 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+388C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728816 | |||||||
chr12:131728846 | C | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+418C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728846 | |||||||
chr12:131729028 | C | T | 58 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(55): Show |
58 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1081+600C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729028 | |||||||
chr12:131729163 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1081+735G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729163 | |||||||
chr12:131729337 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1081+909T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729337 | |||||||
chr12:131729516 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1081+1088G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729516 | |||||||
chr12:131729599 | A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+1171A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729599 | |||||||
chr12:131729643 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1081+1215G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729643 | |||||||
chr12:131729668 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+1240G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729668 | |||||||
chr12:131729943 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1081+1515C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729943 | |||||||
chr12:131730029 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+1601A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730029 | |||||||
chr12:131730043 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1081+1615A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730043 | |||||||
chr12:131730140 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1081+1712G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730140 | |||||||
chr12:131730255 | C | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1081+1827C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730255 | |||||||
chr12:131730318 | G | T | 1 | a0001c0001t0002g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1081+1890G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730318 | |||||||
chr12:131730344 | T | C | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+1916T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730344 | |||||||
chr12:131730355 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+1927G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730355 | |||||||
chr12:131730426 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1081+1998G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730426 | |||||||
chr12:131730494 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1081+2066C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730494 | |||||||
chr12:131730630 | G | T | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1081+2202G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730630 | |||||||
chr12:131730648 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1081+2220C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730648 | |||||||
chr12:131731022 | C | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+2594C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731022 | |||||||
chr12:131731174 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2746A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731174 | |||||||
chr12:131731175 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2747T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731175 | |||||||
chr12:131731176 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2748A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731176 | |||||||
chr12:131731222 | G | A | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1081+2794G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731222 | |||||||
chr12:131731235 | G | A | 19 | a0001c0001t0001g0090 a0001c0001t0002g0082 a0001c0001t0002g0084 others(16): Show |
19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1081+2807G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731235 | |||||||
chr12:131731316 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1081+2888A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731316 | |||||||
chr12:131731799 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(65): Show |
69 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1081+3371A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731799 | |||||||
chr12:131731824 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1081+3396T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731824 | |||||||
chr12:131731849 | C | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1081+3421C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731849 | |||||||
chr12:131731901 | C | CT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(82): Show |
86 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1081+3499dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | ||||||
chr12:131731901 | C | CTT | 27 | a0001c0001t0001g0122 a0001c0001t0001g0153 a0001c0001t0001g0154 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1081+3498_1081+349 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | ||||||
chr12:131731901 | CT | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1081+3499delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | ||||||
chr12:131732013 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1081+3585G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732013 | |||||||
chr12:131732148 | G | A | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1081+3720G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732148 | |||||||
chr12:131732163 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1081+3735G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732163 | |||||||
chr12:131732199 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+3771G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732199 | |||||||
chr12:131732608 | C | T | 1 | a0004c0009t0001g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1081+4180C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732608 | |||||||
chr12:131732902 | ACT | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(79): Show |
83 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1081+4478_1081+447 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131732902 | ||||||
chr12:131732930 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1081+4502C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732930 | |||||||
chr12:131732950 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1081+4522G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732950 | |||||||
chr12:131732988 | G | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1081+4560G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732988 | |||||||
chr12:131733190 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1081+4762G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733190 | |||||||
chr12:131733225 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1081+4797G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733225 | |||||||
chr12:131733296 | C | T | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1081+4868C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733296 | |||||||
chr12:131733333 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG00323.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1081+4905C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733333 | |||||||
chr12:131733396 | C | T | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1081+4968C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733396 | |||||||
chr12:131733408 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1081+4980A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733408 | |||||||
chr12:131733442 | G | A | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+5014G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733442 | |||||||
chr12:131733470 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1081+5042C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733470 | |||||||
chr12:131733497 | A | C | 22 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081+5069A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733497 | |||||||
chr12:131733639 | A | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+5211A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733639 | |||||||
chr12:131733773 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
55 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1081+5345G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733773 | |||||||
chr12:131733907 | C | T | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+5479C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733907 | |||||||
chr12:131734030 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1081+5602A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734030 | |||||||
chr12:131734041 | C | G | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+5613C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734041 | |||||||
chr12:131734176 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+5748A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734176 | |||||||
chr12:131734192 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+5764G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734192 | |||||||
chr12:131734482 | G | A | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1081+6054G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734482 | |||||||
chr12:131734535 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1081+6107C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734535 | |||||||
chr12:131734541 | CAT | C | 8 | a0001c0001t0001g0181 a0001c0001t0002g0084 a0001c0001t0002g0091 others(5): Show |
8 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081+6114_1081+611 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734541 | |||||||
chr12:131734655 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1081+6227G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734655 | |||||||
chr12:131734788 | TCTCCCTG others(75): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1081+6362_1081+644 others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131734788 | ||||||
chr12:131734872 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1081+6444C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734872 | |||||||
chr12:131734882 | A | G | 25 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(22): Show |
25 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1081+6454A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734882 | |||||||
chr12:131734898 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1081+6470C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734898 | |||||||
chr12:131734923 | A | AG | 10 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0158 others(7): Show |
10 | HG00639.hp1 HG01934.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1081+6502dupG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131734923 | ||||||
chr12:131735209 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+6781C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735209 | |||||||
chr12:131735245 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1081+6817C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735245 | |||||||
chr12:131735247 | G | A | 53 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(50): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.1081+6819G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735247 | |||||||
chr12:131735249 | G | A | 2 | a0001c0001t0002g0019 a0001c0004t0001g0099 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1081+6821G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735249 | |||||||
chr12:131735262 | T | G | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+6834T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735262 | |||||||
chr12:131735425 | T | G | 1 | a0008c0023t0001g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1081+6997T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735425 | |||||||
chr12:131735545 | G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1081+7117G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735545 | |||||||
chr12:131735561 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1081+7133G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735561 | |||||||
chr12:131735684 | C | G | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+7256C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735684 | |||||||
chr12:131735750 | G | A | 18 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(15): Show |
18 | HG00639.hp1 HG01943.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1081+7322G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735750 | |||||||
chr12:131735802 | T | C | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+7374T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735802 | |||||||
chr12:131735840 | T | G | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0002t0001g0283 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1081+7412T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735840 | |||||||
chr12:131736039 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp2 HG02148.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1081+7611C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736039 | |||||||
chr12:131736287 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1081+7859G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736287 | |||||||
chr12:131736311 | A | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1081+7883A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736311 | |||||||
chr12:131736401 | A | T | 62 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(59): Show |
62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1081+7973A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736401 | |||||||
chr12:131736414 | A | G | 4 | a0001c0001t0001g0182 a0001c0006t0001g0015 a0001c0019t0001g0188 others(1): Show |
4 | HG02735.hp1 HG02922.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+7986A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736414 | |||||||
chr12:131736488 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1081+8060G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736488 | |||||||
chr12:131736514 | C | T | 62 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(59): Show |
62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1081+8086C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736514 | |||||||
chr12:131736570 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1081+8142G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736570 | |||||||
chr12:131736583 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+8155G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736583 | |||||||
chr12:131736690 | CAT | C | 16 | a0001c0001t0001g0090 a0001c0001t0002g0084 a0001c0001t0002g0085 others(13): Show |
16 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1081+8264_1081+826 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131736690 | ||||||
chr12:131736718 | T | C | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+8290T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736718 | |||||||
chr12:131736751 | G | A | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+8323G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736751 | |||||||
chr12:131736822 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1081+8394A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736822 | |||||||
chr12:131737126 | G | T | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1081+8698G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737126 | |||||||
chr12:131737147 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1081+8719G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737147 | |||||||
chr12:131737236 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1081+8808G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737236 | |||||||
chr12:131737259 | G | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+8831G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737259 | |||||||
chr12:131737526 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1081+9098A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737526 | |||||||
chr12:131737674 | G | A | 50 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(47): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1081+9246G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737674 | |||||||
chr12:131737731 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1081+9303C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737731 | |||||||
chr12:131737743 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+9315T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737743 | |||||||
chr12:131738283 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1081+9855A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738283 | |||||||
chr12:131738288 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+9860G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738288 | |||||||
chr12:131738562 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+10134G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738562 | |||||||
chr12:131738629 | T | G | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1081+10201T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738629 | |||||||
chr12:131738799 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1081+10371G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738799 | |||||||
chr12:131738885 | C | CT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
47 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1081+10481dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0174 others(4): Show |
9 | HG02109.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081+10480_1081+10 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0116 a0001c0001t0001g0231 a0001c0001t0001g0271 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1081+10471_1081+10 others(17): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(5): Show |
44 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1081+10470_1081+10 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(6): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0106 others(47): Show |
51 | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1081+10469_1081+10 others(19): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(7): Show |
30 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0108 others(27): Show |
30 | HG00323.hp2 HG00609.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1081+10468_1081+10 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(8): Show |
10 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0144 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081+10467_1081+10 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG02602.hp2 HG02630.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081+10466_1081+10 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0164 a0001c0001t0001g0228 |
3 | HG02148.hp1 NA18941.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1081+10465_1081+10 others(23): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0001g0166 a0001c0001t0001g0277 a0001c0004t0002g0306 others(1): Show |
4 | HG01943.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+10464_1081+10 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1081+10459_1081+10 others(29): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | CTTT | C | 53 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0063 others(50): Show |
53 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1081+10479_1081+10 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738885 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+10467_1081+10 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | ||||||
chr12:131738933 | A | G | 1 | a0001c0006t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1081+10505A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738933 | |||||||
chr12:131738948 | C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+10520C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738948 | |||||||
chr12:131738975 | C | CCTCAACC others(7): Show |
291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(288): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1081+10552_1081+10 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738975 | ||||||
chr12:131739033 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1081+10605C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739033 | |||||||
chr12:131739128 | T | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(79): Show |
83 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.1081+10700T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739128 | |||||||
chr12:131739238 | A | G | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+10810A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739238 | |||||||
chr12:131739281 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0005g0222 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1081+10853A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739281 | |||||||
chr12:131739335 | G | C | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+10907G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739335 | |||||||
chr12:131739486 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
54 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1081+11058A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739486 | |||||||
chr12:131739499 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1081+11071T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739499 | |||||||
chr12:131739536 | C | CT | 46 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0124 others(43): Show |
47 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1081+11136dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CT | C | 23 | a0001c0001t0001g0012 a0001c0001t0001g0105 a0001c0001t0001g0106 others(20): Show |
23 | HG02027.hp1 HG02486.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.1081+11136delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTT | C | 29 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0072 others(26): Show |
29 | HG00639.hp1 HG01106.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1081+11135_1081+11 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTT | C | 19 | a0001c0001t0001g0048 a0001c0001t0001g0063 a0001c0001t0001g0066 others(16): Show |
19 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1081+11134_1081+11 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1081+11127_1081+11 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTTTTTT others(4): Show |
C | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1081+11126_1081+11 others(17): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1081+11125_1081+11 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG01175.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081+11123_1081+11 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739536 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1081+11122_1081+11 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | ||||||
chr12:131739622 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+11194T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739622 | |||||||
chr12:131739634 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1081+11206C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739634 | |||||||
chr12:131739700 | C | T | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+11272C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739700 | |||||||
chr12:131739707 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+11279G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739707 | |||||||
chr12:131739735 | G | C | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+11307G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739735 | |||||||
chr12:131739834 | C | T | 2 | a0004c0009t0001g0053 a0008c0023t0001g0051 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1081+11406C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739834 | |||||||
chr12:131739882 | G | A | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1081+11454G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739882 | |||||||
chr12:131740048 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1081+11620G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740048 | |||||||
chr12:131740062 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+11634G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740062 | |||||||
chr12:131740230 | T | A | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1081+11802T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740230 | |||||||
chr12:131740245 | A | C | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081+11817A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740245 | |||||||
chr12:131740438 | T | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+12010T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740438 | |||||||
chr12:131740459 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1081+12031A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740459 | |||||||
chr12:131740531 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+12103C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740531 | |||||||
chr12:131740671 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1081+12243G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740671 | |||||||
chr12:131740837 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1082-12286C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740837 | |||||||
chr12:131740966 | C | CT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0102 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1082-12133dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | ||||||
chr12:131740966 | C | CTT | 7 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0001g0146 others(4): Show |
7 | HG00642.hp1 HG01952.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1082-12134_1082-12 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | ||||||
chr12:131740966 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1082-12149_1082-12 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | ||||||
chr12:131740966 | CT | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
55 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1082-12133delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | ||||||
chr12:131740966 | CTTTTTTT | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0175 a0001c0001t0001g0234 others(5): Show |
8 | HG01257.hp1 HG01258.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082-12139_1082-12 others(13): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | ||||||
chr12:131740967 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1082-12148_1082-12 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740967 | ||||||
chr12:131740973 | T | C | 4 | a0001c0001t0002g0054 a0001c0001t0002g0058 a0001c0001t0002g0091 others(1): Show |
4 | HG02027.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-12150T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740973 | |||||||
chr12:131741218 | G | A | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-11905G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741218 | |||||||
chr12:131741237 | A | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-11886A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741237 | |||||||
chr12:131741259 | C | T | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-11864C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741259 | |||||||
chr12:131741398 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1082-11725G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741398 | |||||||
chr12:131741505 | C | T | 62 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1082-11618C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741505 | |||||||
chr12:131741601 | G | T | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-11522G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741601 | |||||||
chr12:131741644 | C | CA | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1082-11463dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131741644 | ||||||
chr12:131741687 | G | A | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-11436G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741687 | |||||||
chr12:131741720 | G | A | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-11403G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741720 | |||||||
chr12:131741924 | C | T | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1082-11199C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741924 | |||||||
chr12:131742013 | A | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1082-11110A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742013 | |||||||
chr12:131742263 | G | A | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-10860G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742263 | |||||||
chr12:131742297 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0157 |
2 | HG01978.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1082-10826A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742297 | |||||||
chr12:131742440 | T | C | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-10683T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742440 | |||||||
chr12:131742513 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1082-10610G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742513 | |||||||
chr12:131742528 | G | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1082-10595G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742528 | |||||||
chr12:131742593 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1082-10530A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742593 | |||||||
chr12:131742633 | CT | C | 23 | a0001c0001t0001g0153 a0001c0001t0002g0310 a0001c0002t0001g0283 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1082-10476delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131742633 | ||||||
chr12:131742661 | G | A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1082-10462G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742661 | |||||||
chr12:131742664 | G | T | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-10459G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742664 | |||||||
chr12:131742683 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1082-10440C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742683 | |||||||
chr12:131743208 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-9915G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743208 | |||||||
chr12:131743223 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1082-9900C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743223 | |||||||
chr12:131743303 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1082-9820C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743303 | |||||||
chr12:131743446 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-9677A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743446 | |||||||
chr12:131743504 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0004t0002g0306 others(1): Show |
4 | HG01243.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-9619G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743504 | |||||||
chr12:131743516 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1082-9607C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743516 | |||||||
chr12:131743560 | G | A | 5 | a0001c0001t0003g0031 a0001c0001t0003g0308 a0001c0001t0004g0305 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082-9563G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743560 | |||||||
chr12:131743929 | C | T | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1082-9194C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743929 | |||||||
chr12:131744068 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1082-9055G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744068 | |||||||
chr12:131744177 | C | T | 2 | a0001c0002t0001g0287 a0001c0002t0001g0288 |
2 | HG02293.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1082-8946C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744177 | |||||||
chr12:131744446 | C | G | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-8677C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744446 | |||||||
chr12:131744713 | A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-8410A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744713 | |||||||
chr12:131744788 | A | G | 55 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(52): Show |
55 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1082-8335A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744788 | |||||||
chr12:131744807 | A | G | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-8316A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744807 | |||||||
chr12:131744912 | T | G | 3 | a0001c0001t0001g0233 a0001c0008t0001g0235 a0001c0008t0001g0236 |
3 | HG00733.hp2 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1082-8211T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744912 | |||||||
chr12:131744962 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-8161G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744962 | |||||||
chr12:131745018 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1082-8105A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745018 | |||||||
chr12:131745195 | G | A | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-7928G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745195 | |||||||
chr12:131745430 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1082-7693G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745430 | |||||||
chr12:131745557 | G | A | 1 | a0002c0003t0004g0022 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1082-7566G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745557 | |||||||
chr12:131745630 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18960.hp1 NA19065.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-7493G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745630 | |||||||
chr12:131745754 | C | CT | 11 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0182 others(8): Show |
11 | HG00741.hp1 HG01099.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1082-7356dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131745754 | ||||||
chr12:131745947 | G | C | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-7176G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745947 | |||||||
chr12:131745960 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1082-7163C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745960 | |||||||
chr12:131746082 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(78): Show |
82 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1082-7041C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746082 | |||||||
chr12:131746312 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1082-6811C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746312 | |||||||
chr12:131746319 | G | A | 2 | a0001c0001t0001g0160 a0004c0009t0001g0052 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1082-6804G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746319 | |||||||
chr12:131746376 | G | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-6747G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746376 | |||||||
chr12:131746691 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-6432A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746691 | |||||||
chr12:131746704 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-6419A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746704 | |||||||
chr12:131746827 | G | A | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-6296G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746827 | |||||||
chr12:131746875 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1082-6248C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746875 | |||||||
chr12:131746921 | G | A | 1 | a0001c0002t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1082-6202G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746921 | |||||||
chr12:131746931 | G | C | 50 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(47): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1082-6192G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746931 | |||||||
chr12:131746932 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | NA18942.hp1 NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1082-6191G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746932 | |||||||
chr12:131746955 | T | G | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1082-6168T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746955 | |||||||
chr12:131746961 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1082-6162G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746961 | |||||||
chr12:131746964 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0130 |
2 | HG03239.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1082-6159T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746964 | |||||||
chr12:131746972 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1082-6151C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746972 | |||||||
chr12:131746976 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1082-6147T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746976 | |||||||
chr12:131747021 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1082-6102A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747021 | |||||||
chr12:131747023 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1082-6100C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747023 | |||||||
chr12:131747036 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
70 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1082-6087A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747036 | |||||||
chr12:131747083 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1082-6040A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747083 | |||||||
chr12:131747103 | C | CAAAAAAA others(2): Show |
61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0047 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1082-6012_1082-600 others(13): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | ||||||
chr12:131747103 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0002g0050 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1082-6013_1082-600 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | ||||||
chr12:131747103 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0002g0097 a0001c0004t0001g0099 a0001c0004t0002g0011 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1082-6014_1082-600 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | ||||||
chr12:131747138 | A | C | 97 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0047 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1082-5985A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747138 | |||||||
chr12:131747140 | C | T | 14 | a0001c0001t0002g0095 a0001c0001t0003g0018 a0001c0001t0003g0025 others(11): Show |
14 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1082-5983C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747140 | |||||||
chr12:131747167 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(166): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1082-5956T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747167 | |||||||
chr12:131747212 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-5911G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747212 | |||||||
chr12:131747477 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1082-5646G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747477 | |||||||
chr12:131747615 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-5508T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747615 | |||||||
chr12:131747743 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1082-5380G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747743 | |||||||
chr12:131747826 | T | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-5297T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747826 | |||||||
chr12:131747830 | G | A | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-5293G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747830 | |||||||
chr12:131748218 | C | CT | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1082-4890dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | ||||||
chr12:131748218 | C | CTT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0047 others(83): Show |
87 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1082-4891_1082-489 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | ||||||
chr12:131748218 | CT | C | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-4890delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | ||||||
chr12:131748258 | C | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4865C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748258 | |||||||
chr12:131748425 | G | T | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-4698G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748425 | |||||||
chr12:131748490 | T | C | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1082-4633T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748490 | |||||||
chr12:131748512 | A | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4611A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748512 | |||||||
chr12:131748598 | A | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(80): Show |
84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-4525A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748598 | |||||||
chr12:131748797 | C | T | 1 | a0014c0030t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1082-4326C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748797 | |||||||
chr12:131748914 | A | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4209A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748914 | |||||||
chr12:131748946 | A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4177A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748946 | |||||||
chr12:131749021 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1082-4102A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749021 | |||||||
chr12:131749062 | A | C | 56 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-4061A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749062 | |||||||
chr12:131749113 | T | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0118 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1082-4010T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749113 | |||||||
chr12:131749144 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1082-3979C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749144 | |||||||
chr12:131749174 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1082-3949C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749174 | |||||||
chr12:131749257 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1082-3866G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749257 | |||||||
chr12:131749287 | G | T | 7 | a0001c0004t0001g0099 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-3836G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749287 | |||||||
chr12:131749310 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1082-3813C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749310 | |||||||
chr12:131749313 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1082-3810C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749313 | |||||||
chr12:131749667 | A | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1082-3456A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749667 | |||||||
chr12:131749739 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0083 |
2 | HG00733.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1082-3384G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749739 | |||||||
chr12:131749836 | A | C | 1 | a0001c0001t0003g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1082-3287A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749836 | |||||||
chr12:131750055 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1082-3068C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750055 | |||||||
chr12:131750157 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1082-2966C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750157 | |||||||
chr12:131750277 | C | G | 1 | a0001c0011t0002g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1082-2846C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750277 | |||||||
chr12:131750373 | G | A | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-2750G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750373 | |||||||
chr12:131750481 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-2642G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750481 | |||||||
chr12:131750519 | T | TC | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-2602dupC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131750519 | ||||||
chr12:131750540 | G | A | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1082-2583G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750540 | |||||||
chr12:131750553 | G | A | 6 | a0001c0001t0003g0018 a0001c0001t0003g0025 a0001c0001t0003g0031 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1082-2570G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750553 | |||||||
chr12:131750891 | TGG | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0002t0001g0283 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2231_1082-223 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750891 | |||||||
chr12:131750895 | AT | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0002t0001g0283 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2226delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131750895 | ||||||
chr12:131750897 | T | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0002t0001g0283 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2226T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750897 | |||||||
chr12:131750921 | A | G | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-2202A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750921 | |||||||
chr12:131750927 | G | T | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1082-2196G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750927 | |||||||
chr12:131750947 | T | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-2176T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750947 | |||||||
chr12:131751072 | G | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1082-2051G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751072 | |||||||
chr12:131751127 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1082-1996G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751127 | |||||||
chr12:131751314 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-1809C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751314 | |||||||
chr12:131751349 | C | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1082-1774C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751349 | |||||||
chr12:131751398 | G | A | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-1725G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751398 | |||||||
chr12:131751413 | G | T | 7 | a0001c0001t0001g0149 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-1710G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751413 | |||||||
chr12:131751445 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0010t0004g0023 |
3 | HG01243.hp1 HG01261.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-1678G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751445 | |||||||
chr12:131751604 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0179 |
3 | HG01243.hp1 HG03098.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1082-1519C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751604 | |||||||
chr12:131751687 | A | C | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-1436A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751687 | |||||||
chr12:131751873 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1082-1250C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751873 | |||||||
chr12:131751961 | G | A | 21 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-1162G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751961 | |||||||
chr12:131752057 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-1066C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752057 | |||||||
chr12:131752104 | A | G | 4 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-1019A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752104 | |||||||
chr12:131752291 | C | T | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-832C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752291 | |||||||
chr12:131752392 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1082-731G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752392 | |||||||
chr12:131752478 | C | G | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-645C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752478 | |||||||
chr12:131752788 | C | A | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0297 |
3 | HG00099.hp2 HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1082-335C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752788 | |||||||
chr12:131752790 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(8): Show |
11 | HG02040.hp2 HG02056.hp2 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1082-333C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752790 | |||||||
chr12:131753057 | G | A | 3 | a0001c0012t0001g0044 a0001c0012t0001g0045 a0001c0031t0001g0046 |
3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-66G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131753057 | |||||||
chr12:131753424 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1322+61C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753424 | |||||||
chr12:131753501 | A | G | 1 | a0001c0011t0002g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1322+138A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753501 | |||||||
chr12:131753580 | T | A | 19 | a0001c0001t0001g0090 a0001c0001t0002g0082 a0001c0001t0002g0084 others(16): Show |
19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1322+217T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753580 | |||||||
chr12:131753580 | T | C | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1322+217T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753580 | |||||||
chr12:131753609 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1322+246T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753609 | |||||||
chr12:131753683 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1322+320T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753683 | |||||||
chr12:131753714 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1322+351A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753714 | |||||||
chr12:131753834 | C | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1322+471C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753834 | |||||||
chr12:131753852 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1322+489C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753852 | |||||||
chr12:131753893 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1323-475C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753893 | |||||||
chr12:131753979 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1323-389C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753979 | |||||||
chr12:131754061 | A | G | 1 | a0001c0010t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1323-307A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754061 | |||||||
chr12:131754288 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1323-80C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754288 | |||||||
chr12:131754301 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0002g0050 |
2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1323-67C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754301 | |||||||
chr12:131754562 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1454+63T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754562 | |||||||
chr12:131754627 | C | CT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0047 others(87): Show |
91 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1454+152dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | ||||||
chr12:131754627 | C | CTT | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
91 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1454+151_1454+152d others(4): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | ||||||
chr12:131754627 | C | CTTT | 18 | a0001c0001t0001g0012 a0001c0001t0001g0090 a0001c0001t0001g0180 others(15): Show |
18 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1454+150_1454+152d others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | ||||||
chr12:131754658 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454+159G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754658 | |||||||
chr12:131754678 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1454+179G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754678 | |||||||
chr12:131754779 | G | A | 1 | a0001c0002t0001g0299 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1454+280G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754779 | |||||||
chr12:131754781 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1454+282G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754781 | |||||||
chr12:131754786 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1454+287A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754786 | |||||||
chr12:131754820 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1454+321A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754820 | |||||||
chr12:131754934 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(78): Show |
82 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1454+435A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754934 | |||||||
chr12:131754997 | T | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(70): Show |
74 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1455-389T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754997 | |||||||
chr12:131755191 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
46 | HG00558.hp2 HG00597.hp2 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.1455-195C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755191 | |||||||
chr12:131755209 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1455-177G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755209 | |||||||
chr12:131755353 | T | G | 14 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(11): Show |
14 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1455-33T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755353 | |||||||
chr12:131755528 | G | A | 7 | a0001c0001t0003g0018 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+49G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755528 | |||||||
chr12:131755656 | A | C | 3 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 |
3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1548+177A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755656 | |||||||
chr12:131755728 | A | C | 3 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 |
3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1548+249A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755728 | |||||||
chr12:131755796 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1548+317C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755796 | |||||||
chr12:131755891 | A | G | 7 | a0001c0001t0003g0018 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+412A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755891 | |||||||
chr12:131755900 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1548+421T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755900 | |||||||
chr12:131756114 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1549-359A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756114 | |||||||
chr12:131756119 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1549-354A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756119 | |||||||
chr12:131756196 | C | CAAAGAAA others(335): Show |
1 | a0001c0012t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1549-261_1549-260i others(344): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 131756196 | ||||||
chr12:131756218 | G | C | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1549-255G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756218 | |||||||
chr12:131756249 | G | A | 1 | a0001c0031t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1549-224G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756249 | |||||||
chr12:131756392 | C | CAT | 141 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(138): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1549-77_1549-76dup others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 131756392 | ||||||
chr12:131756684 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1720+40A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756684 | |||||||
chr12:131756757 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1720+113C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756757 | |||||||
chr12:131756817 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0147 a0001c0001t0001g0151 others(3): Show |
6 | HG00597.hp1 HG02155.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1720+173C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756817 | |||||||
chr12:131756819 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1720+175C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756819 | |||||||
chr12:131756820 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1720+176G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756820 | |||||||
chr12:131757106 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1720+462T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757106 | |||||||
chr12:131757232 | G | C | 1 | a0001c0031t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1720+588G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757232 | |||||||
chr12:131757267 | T | G | 1 | a0001c0001t0001g0190 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1720+623T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757267 | |||||||
chr12:131757319 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+675G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757319 | |||||||
chr12:131757503 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1720+859C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757503 | |||||||
chr12:131757600 | G | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1720+956G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757600 | |||||||
chr12:131757702 | T | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1720+1058T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757702 | |||||||
chr12:131757714 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1720+1070G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757714 | |||||||
chr12:131757739 | G | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0062 |
2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1720+1095G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757739 | |||||||
chr12:131757907 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1720+1263G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757907 | |||||||
chr12:131758007 | G | C | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1720+1363G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758007 | |||||||
chr12:131758065 | C | T | 3 | a0001c0008t0001g0235 a0001c0008t0001g0236 a0001c0031t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1720+1421C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758065 | |||||||
chr12:131758623 | G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1720+1979G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758623 | |||||||
chr12:131758712 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1720+2068C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758712 | |||||||
chr12:131758776 | T | G | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1720+2132T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758776 | |||||||
chr12:131759019 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1720+2375G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759019 | |||||||
chr12:131759383 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1720+2739T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759383 | |||||||
chr12:131759499 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1720+2855G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759499 | |||||||
chr12:131759570 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1720+2926C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759570 | |||||||
chr12:131759615 | C | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1720+2971C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759615 | |||||||
chr12:131759641 | T | TA | 36 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(33): Show |
36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1720+3007dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131759641 | ||||||
chr12:131759718 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0003g0021 |
2 | HG02165.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1720+3074C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759718 | |||||||
chr12:131759766 | T | C | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1720+3122T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759766 | |||||||
chr12:131759797 | G | A | 3 | a0001c0008t0001g0235 a0001c0008t0001g0236 a0001c0031t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1720+3153G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759797 | |||||||
chr12:131759853 | A | G | 11 | a0001c0001t0001g0265 a0001c0002t0001g0285 a0001c0002t0001g0287 others(8): Show |
11 | HG00741.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+3209A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759853 | |||||||
chr12:131760015 | A | G | 1 | a0002c0028t0004g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1720+3371A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760015 | |||||||
chr12:131760120 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1720+3476A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760120 | |||||||
chr12:131760256 | C | T | 9 | a0001c0002t0001g0283 a0001c0002t0001g0286 a0001c0002t0001g0289 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+3612C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760256 | |||||||
chr12:131760309 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0207 |
2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1720+3665T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760309 | |||||||
chr12:131760383 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+3739T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760383 | |||||||
chr12:131760481 | A | T | 5 | a0001c0002t0001g0283 a0001c0002t0001g0286 a0001c0002t0001g0289 others(2): Show |
5 | HG00140.hp1 HG00642.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+3837A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760481 | |||||||
chr12:131760869 | C | G | 6 | a0001c0001t0001g0047 a0001c0004t0002g0009 a0001c0004t0002g0010 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-3587C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760869 | |||||||
chr12:131760987 | G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1721-3469G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760987 | |||||||
chr12:131761007 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-3449A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761007 | |||||||
chr12:131761011 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1721-3445G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761011 | |||||||
chr12:131761097 | C | T | 6 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-3359C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761097 | |||||||
chr12:131761176 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1721-3280T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761176 | |||||||
chr12:131761360 | C | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-3096C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761360 | |||||||
chr12:131761380 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1721-3076C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761380 | |||||||
chr12:131761436 | G | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(126): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1721-3020G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761436 | |||||||
chr12:131761548 | G | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1721-2908G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761548 | |||||||
chr12:131761613 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1721-2843G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761613 | |||||||
chr12:131761638 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-2818C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761638 | |||||||
chr12:131761756 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1721-2700C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761756 | |||||||
chr12:131761862 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1721-2594C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761862 | |||||||
chr12:131761955 | T | A | 26 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1721-2501T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761955 | |||||||
chr12:131761998 | C | T | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1721-2458C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761998 | |||||||
chr12:131762202 | C | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1721-2254C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762202 | |||||||
chr12:131762371 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1721-2085A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762371 | |||||||
chr12:131762613 | A | G | 4 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-1843A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762613 | |||||||
chr12:131762637 | G | T | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1721-1819G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762637 | |||||||
chr12:131762650 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-1806A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762650 | |||||||
chr12:131762709 | C | G | 18 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(15): Show |
18 | HG00639.hp1 HG01943.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1721-1747C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762709 | |||||||
chr12:131762966 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01123.hp1 HG01261.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-1490C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762966 | |||||||
chr12:131763146 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1721-1310C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763146 | |||||||
chr12:131763176 | A | G | 3 | a0001c0008t0001g0235 a0001c0008t0001g0236 a0001c0031t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1721-1280A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763176 | |||||||
chr12:131763223 | C | T | 48 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1721-1233C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763223 | |||||||
chr12:131763409 | C | G | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0297 |
3 | HG00099.hp2 HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1721-1047C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763409 | |||||||
chr12:131763587 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1721-869C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763587 | |||||||
chr12:131763636 | CA | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0250 a0001c0001t0001g0253 others(2): Show |
6 | HG02015.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-819delA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763636 | |||||||
chr12:131763703 | T | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1721-753T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763703 | |||||||
chr12:131763757 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1721-699A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763757 | |||||||
chr12:131763790 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1721-666A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763790 | |||||||
chr12:131763815 | A | AT | 27 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0066 others(24): Show |
27 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1721-624dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131763815 | ||||||
chr12:131763815 | AT | A | 11 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(8): Show |
11 | HG00099.hp2 HG01106.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1721-624delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131763815 | ||||||
chr12:131764098 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1721-358C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764098 | |||||||
chr12:131764306 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-150C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764306 | |||||||
chr12:131764334 | G | C | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1721-122G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764334 | |||||||
chr12:131764898 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1951+212G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764898 | |||||||
chr12:131764943 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1951+257T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764943 | |||||||
chr12:131764952 | A | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01123.hp1 HG01261.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951+266A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764952 | |||||||
chr12:131765042 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1951+356A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765042 | |||||||
chr12:131765250 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1951+564C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765250 | |||||||
chr12:131765251 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1951+565A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765251 | |||||||
chr12:131765269 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1951+583G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765269 | |||||||
chr12:131765463 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1952-655A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765463 | |||||||
chr12:131765668 | C | G | 22 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1952-450C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765668 | |||||||
chr12:131765815 | T | TCTC | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1952-303_1952-302i others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765815 | |||||||
chr12:131765967 | T | C | 1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1952-151T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765967 | |||||||
chr12:131766043 | C | T | 1 | a0004c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1952-75C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131766043 | |||||||
chr12:131766104 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1952-14G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131766104 | |||||||
chr12:131766326 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2142+18A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766326 | |||||||
chr12:131766521 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2142+213C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766521 | |||||||
chr12:131766532 | G | T | 1 | a0004c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2142+224G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766532 | |||||||
chr12:131766637 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2142+329A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766637 | |||||||
chr12:131766712 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+404G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766712 | |||||||
chr12:131766954 | TGTGTCCG others(56): Show |
T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2142+860_2142+922d others(65): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131766954 | ||||||
chr12:131767014 | A | T | 6 | a0001c0001t0001g0196 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2142+706A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767014 | |||||||
chr12:131767017 | C | T | 7 | a0001c0001t0001g0196 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142+709C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767017 | |||||||
chr12:131767019 | T | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2142+711T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767019 | |||||||
chr12:131767143 | C | T | 4 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0297 others(1): Show |
4 | HG00099.hp2 HG00639.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+835C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767143 | |||||||
chr12:131767186 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2142+878C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767186 | |||||||
chr12:131767212 | C | T | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2142+904C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767212 | |||||||
chr12:131767238 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2142+930A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767238 | |||||||
chr12:131767842 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2142+1534G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767842 | |||||||
chr12:131767965 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2142+1657T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767965 | |||||||
chr12:131768027 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+1719G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768027 | |||||||
chr12:131768030 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2142+1722A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768030 | |||||||
chr12:131768118 | T | C | 28 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(25): Show |
28 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2142+1810T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768118 | |||||||
chr12:131768230 | G | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+1922G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768230 | |||||||
chr12:131768237 | C | T | 1 | a0002c0003t0004g0022 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2142+1929C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768237 | |||||||
chr12:131768517 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2142+2209G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768517 | |||||||
chr12:131768568 | C | G | 17 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(14): Show |
17 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.2142+2260C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768568 | |||||||
chr12:131768573 | G | A | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2142+2265G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768573 | |||||||
chr12:131768600 | C | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+2292C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768600 | |||||||
chr12:131768631 | C | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2142+2323C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768631 | |||||||
chr12:131768680 | C | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+2372C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768680 | |||||||
chr12:131768681 | G | C | 2 | a0001c0001t0001g0279 a0006c0020t0001g0280 |
2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2142+2373G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768681 | |||||||
chr12:131768820 | C | T | 22 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(19): Show |
22 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2142+2512C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768820 | |||||||
chr12:131768824 | G | T | 2 | a0002c0003t0003g0041 a0002c0028t0004g0309 |
2 | HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2142+2516G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768824 | |||||||
chr12:131768955 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2142+2647G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768955 | |||||||
chr12:131769020 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+2712G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769020 | |||||||
chr12:131769055 | A | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0282 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2142+2747A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769055 | |||||||
chr12:131769113 | C | T | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2142+2805C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769113 | |||||||
chr12:131769126 | C | CA | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2142+2829dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131769126 | ||||||
chr12:131769309 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2142+3001G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769309 | |||||||
chr12:131769437 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2142+3129A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769437 | |||||||
chr12:131769441 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+3133C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769441 | |||||||
chr12:131769448 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2142+3140T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769448 | |||||||
chr12:131769458 | C | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG01175.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+3150C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769458 | |||||||
chr12:131769604 | A | ATTTAT | 3 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 |
3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2142+3309_2142+331 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131769604 | ||||||
chr12:131769634 | G | A | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2142+3326G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769634 | |||||||
chr12:131769720 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+3412G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769720 | |||||||
chr12:131769754 | G | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2142+3446G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769754 | |||||||
chr12:131769787 | C | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2142+3479C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769787 | |||||||
chr12:131769853 | T | C | 3 | a0001c0001t0002g0019 a0001c0012t0001g0044 a0001c0012t0001g0045 |
3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2142+3545T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769853 | |||||||
chr12:131769883 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2142+3575A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769883 | |||||||
chr12:131770045 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+3737T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770045 | |||||||
chr12:131770235 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+3927G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770235 | |||||||
chr12:131770276 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2142+3968A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770276 | |||||||
chr12:131770369 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2142+4061C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770369 | |||||||
chr12:131770391 | T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+4083T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770391 | |||||||
chr12:131770622 | A | AT | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2142+4321dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131770622 | ||||||
chr12:131770906 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2142+4598C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770906 | |||||||
chr12:131770911 | G | T | 4 | a0001c0004t0001g0099 a0001c0008t0001g0235 a0001c0008t0001g0236 others(1): Show |
4 | HG00733.hp2 HG01175.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+4603G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770911 | |||||||
chr12:131771048 | C | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2142+4740C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771048 | |||||||
chr12:131771064 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0153 |
2 | NA18939.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2142+4756G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771064 | |||||||
chr12:131771387 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2142+5079A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771387 | |||||||
chr12:131771650 | C | CT | 7 | a0001c0001t0002g0084 a0001c0001t0002g0091 a0001c0001t0002g0092 others(4): Show |
7 | HG01934.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5364dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | ||||||
chr12:131771650 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.2142+5364delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | ||||||
chr12:131771650 | CTT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2142+5363_2142+536 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | ||||||
chr12:131771711 | T | TAGCGCGA others(4): Show |
1 | a0001c0001t0001g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2142+5404_2142+541 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771711 | ||||||
chr12:131771715 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0079 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2142+5407G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771715 | |||||||
chr12:131771723 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5415G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771723 | |||||||
chr12:131771729 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2142+5421A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771729 | |||||||
chr12:131771802 | A | G | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2142+5494A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771802 | |||||||
chr12:131771812 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5504G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771812 | |||||||
chr12:131771820 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | NA18995.hp2 NA19003.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2142+5512G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771820 | |||||||
chr12:131771931 | G | A | 2 | a0001c0008t0001g0235 a0001c0008t0001g0236 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2142+5623G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771931 | |||||||
chr12:131771949 | C | G | 22 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2142+5641C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771949 | |||||||
chr12:131771957 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2142+5649G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771957 | |||||||
chr12:131772026 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0002g0019 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2142+5718A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772026 | |||||||
chr12:131772036 | G | C | 1 | a0001c0006t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2142+5728G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772036 | |||||||
chr12:131772051 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+5743C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772051 | |||||||
chr12:131772166 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2142+5858C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772166 | |||||||
chr12:131772189 | C | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2143-5876C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772189 | |||||||
chr12:131772279 | T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-5786T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772279 | |||||||
chr12:131772325 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2143-5740A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772325 | |||||||
chr12:131772442 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2143-5623A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772442 | |||||||
chr12:131772473 | G | A | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-5592G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772473 | |||||||
chr12:131772618 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-5447C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772618 | |||||||
chr12:131772619 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-5446G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772619 | |||||||
chr12:131772630 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2143-5435G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772630 | |||||||
chr12:131772805 | T | C | 37 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(34): Show |
37 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.2143-5260T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772805 | |||||||
chr12:131772811 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-5254G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772811 | |||||||
chr12:131773110 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2143-4955G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773110 | |||||||
chr12:131773201 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2143-4864A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773201 | |||||||
chr12:131773225 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-4840G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773225 | |||||||
chr12:131773232 | C | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-4833C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773232 | |||||||
chr12:131773309 | G | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-4756G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773309 | |||||||
chr12:131773400 | T | TA | 9 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(6): Show |
10 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2143-4664dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131773400 | ||||||
chr12:131773410 | G | GCTCACTG others(4): Show |
3 | a0004c0009t0001g0052 a0004c0009t0001g0053 a0008c0023t0001g0051 |
3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2143-4652_2143-464 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131773410 | ||||||
chr12:131773748 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0158 |
2 | NA18941.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2143-4317T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773748 | |||||||
chr12:131773883 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2143-4182G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773883 | |||||||
chr12:131773889 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2143-4176G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773889 | |||||||
chr12:131774204 | G | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-3861G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774204 | |||||||
chr12:131774254 | A | G | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-3811A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774254 | |||||||
chr12:131774315 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2143-3750A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774315 | |||||||
chr12:131774513 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2143-3552G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774513 | |||||||
chr12:131774536 | G | A | 1 | a0002c0003t0003g0033 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2143-3529G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774536 | |||||||
chr12:131774567 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143-3498G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774567 | |||||||
chr12:131774749 | AC | A | 22 | a0001c0002t0001g0283 a0001c0002t0001g0285 a0001c0002t0001g0286 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2143-3314delC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131774749 | ||||||
chr12:131774877 | T | C | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2143-3188T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774877 | |||||||
chr12:131774959 | G | A | 5 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.2143-3106G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774959 | |||||||
chr12:131774962 | A | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3103A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774962 | |||||||
chr12:131774963 | G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3102G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774963 | |||||||
chr12:131775005 | G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3060G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775005 | |||||||
chr12:131775133 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2143-2932C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775133 | |||||||
chr12:131775258 | G | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-2807G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775258 | |||||||
chr12:131775284 | C | T | 3 | a0001c0008t0001g0235 a0001c0008t0001g0236 a0001c0031t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2143-2781C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775284 | |||||||
chr12:131775297 | T | C | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2143-2768T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775297 | |||||||
chr12:131775363 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-2702C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775363 | |||||||
chr12:131775381 | C | G | 36 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(33): Show |
36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.2143-2684C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775381 | |||||||
chr12:131775401 | C | T | 37 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(34): Show |
37 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.2143-2664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775401 | |||||||
chr12:131775421 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0127 others(3): Show |
6 | HG01978.hp1 HG03831.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2143-2644G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775421 | |||||||
chr12:131775434 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2143-2631C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775434 | |||||||
chr12:131775435 | G | A | 15 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(12): Show |
15 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2143-2630G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775435 | |||||||
chr12:131775757 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2143-2308T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775757 | |||||||
chr12:131775935 | C | CA | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0112 others(6): Show |
9 | HG00597.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2143-2113dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131775935 | ||||||
chr12:131775969 | G | T | 1 | a0001c0001t0003g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143-2096G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775969 | |||||||
chr12:131776008 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2143-2057A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776008 | |||||||
chr12:131776034 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-2031G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776034 | |||||||
chr12:131776062 | A | G | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2143-2003A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776062 | |||||||
chr12:131776076 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2143-1989C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776076 | |||||||
chr12:131776096 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0149 |
2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2143-1969G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776096 | |||||||
chr12:131776097 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0149 |
2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2143-1968C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776097 | |||||||
chr12:131776139 | C | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2143-1926C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776139 | |||||||
chr12:131776327 | G | A | 2 | a0001c0001t0001g0157 a0002c0028t0004g0309 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2143-1738G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776327 | |||||||
chr12:131776554 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0151 |
2 | HG00597.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2143-1511C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776554 | |||||||
chr12:131776556 | G | A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2143-1509G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776556 | |||||||
chr12:131776625 | T | C | 3 | a0001c0001t0001g0182 a0001c0019t0001g0188 a0014c0030t0001g0189 |
3 | HG02735.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2143-1440T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776625 | |||||||
chr12:131776680 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2143-1385C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776680 | |||||||
chr12:131776730 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2143-1335C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776730 | |||||||
chr12:131777145 | AT | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0250 a0001c0001t0001g0253 others(2): Show |
6 | HG02015.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143-911delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131777145 | ||||||
chr12:131777388 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2143-677C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777388 | |||||||
chr12:131777441 | G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-624G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777441 | |||||||
chr12:131777695 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2143-370T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777695 | |||||||
chr12:131777715 | C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-350C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777715 | |||||||
chr12:131778366 | A | T | 21 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.2408+36A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778366 | |||||||
chr12:131778478 | T | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+148T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778478 | |||||||
chr12:131778558 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2408+228C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778558 | |||||||
chr12:131778603 | C | T | 1 | a0010c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2408+273C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778603 | |||||||
chr12:131778678 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2408+348T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778678 | |||||||
chr12:131778807 | C | A | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+477C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778807 | |||||||
chr12:131778846 | A | G | 1 | a0003c0005t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2408+516A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778846 | |||||||
chr12:131778887 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2408+557G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778887 | |||||||
chr12:131779074 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2408+744G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779074 | |||||||
chr12:131779076 | A | G | 3 | a0001c0008t0001g0235 a0001c0008t0001g0236 a0001c0031t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2408+746A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779076 | |||||||
chr12:131779101 | T | TA | 6 | a0001c0001t0001g0196 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2408+772dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779101 | ||||||
chr12:131779104 | A | G | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2408+774A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779104 | |||||||
chr12:131779208 | T | TGTGTATG others(50): Show |
1 | a0001c0001t0001g0247 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2408+882_2408+883i others(59): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTATG others(49): Show |
108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.2408+882_2408+883i others(58): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTATG others(77): Show |
27 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2408+882_2408+883i others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(79): Show |
1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2408+901_2408+902i others(88): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(78): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0170 |
2 | HG01496.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2408+929_2408+930i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(49): Show |
17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0114 others(14): Show |
17 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(58): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(78): Show |
1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2408+933_2408+934i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(77): Show |
70 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(67): Show |
71 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(105): Show |
1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(114): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(161): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0074 |
3 | HG01069.hp2 HG01071.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(189): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0070 |
2 | HG01517.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2408+933_2408+934i others(198): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(162): Show |
1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(171): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(161): Show |
12 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0066 others(9): Show |
12 | HG00323.hp1 HG00733.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(161): Show |
1 | a0004c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779208 | T | TGTGTGTG others(162): Show |
1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2408+928_2408+929i others(171): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | ||||||
chr12:131779230 | G | GGTGAGCG others(78): Show |
1 | a0001c0001t0001g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779230 | ||||||
chr12:131779237 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
62 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.2408+907G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779237 | |||||||
chr12:131779264 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2408+934T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779264 | |||||||
chr12:131779368 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2408+1038G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779368 | |||||||
chr12:131779508 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2408+1178C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779508 | |||||||
chr12:131779565 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2408+1235G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779565 | |||||||
chr12:131779607 | G | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+1277G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779607 | |||||||
chr12:131779614 | C | CT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2408+1285dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779614 | ||||||
chr12:131779880 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+1550A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779880 | |||||||
chr12:131779953 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2408+1623A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779953 | |||||||
chr12:131779995 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2408+1665A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779995 | |||||||
chr12:131780079 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2408+1749C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780079 | |||||||
chr12:131780223 | T | C | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+1893T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780223 | |||||||
chr12:131780342 | G | A | 4 | a0001c0001t0001g0230 a0001c0004t0002g0009 a0001c0004t0002g0010 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2408+2012G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780342 | |||||||
chr12:131780506 | T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2408+2176T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780506 | |||||||
chr12:131780551 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+2221G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780551 | |||||||
chr12:131780621 | G | A | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2408+2291G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780621 | |||||||
chr12:131780687 | T | TA | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+2363dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131780687 | ||||||
chr12:131780719 | G | A | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+2389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780719 | |||||||
chr12:131780890 | G | A | 1 | a0003c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2408+2560G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780890 | |||||||
chr12:131781155 | G | A | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2408+2825G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781155 | |||||||
chr12:131781167 | C | T | 1 | a0001c0006t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2408+2837C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781167 | |||||||
chr12:131781171 | T | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2408+2841T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781171 | |||||||
chr12:131781234 | AT | A | 34 | a0001c0001t0001g0061 a0001c0001t0001g0160 a0001c0001t0002g0054 others(31): Show |
34 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2408+2927delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131781234 | ||||||
chr12:131781235 | T | TTA | 29 | a0001c0001t0001g0229 a0001c0001t0001g0265 a0001c0001t0001g0278 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131781235 | ||||||
chr12:131781236 | T | TA | 137 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781236 | |||||||
chr12:131781236 | T | TATTA | 3 | a0001c0004t0002g0306 a0001c0004t0002g0307 a0001c0015t0002g0008 |
3 | HG02451.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781236 | |||||||
chr12:131781237 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
83 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2408+2907T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781237 | |||||||
chr12:131781238 | T | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0229 a0001c0001t0001g0278 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2408+2908T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781238 | |||||||
chr12:131781239 | T | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2408+2909T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781239 | |||||||
chr12:131781240 | T | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
78 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2408+2910T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781240 | |||||||
chr12:131781241 | T | A | 5 | a0001c0001t0001g0229 a0001c0004t0001g0099 a0001c0008t0001g0235 others(2): Show |
5 | HG00733.hp2 HG01175.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2408+2911T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781241 | |||||||
chr12:131781242 | T | A | 59 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0124 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2408+2912T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781242 | |||||||
chr12:131781243 | T | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
54 | HG00558.hp2 HG00597.hp2 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.2408+2913T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781243 | |||||||
chr12:131781245 | T | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+2915T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781245 | |||||||
chr12:131781246 | T | A | 1 | a0001c0001t0001g0260 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2408+2916T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781246 | |||||||
chr12:131781295 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2408+2965T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781295 | |||||||
chr12:131781299 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2408+2969G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781299 | |||||||
chr12:131781383 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2408+3053G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781383 | |||||||
chr12:131781456 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+3126C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781456 | |||||||
chr12:131781478 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2408+3148C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781478 | |||||||
chr12:131781480 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0002g0019 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2408+3150A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781480 | |||||||
chr12:131781489 | G | A | 36 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(33): Show |
36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.2408+3159G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781489 | |||||||
chr12:131781532 | C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2408+3202C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781532 | |||||||
chr12:131781710 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0025 a0001c0001t0003g0031 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2408+3380G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781710 | |||||||
chr12:131781789 | C | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2408+3459C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781789 | |||||||
chr12:131781904 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2408+3574C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781904 | |||||||
chr12:131782004 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2408+3674C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782004 | |||||||
chr12:131782118 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2408+3788G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782118 | |||||||
chr12:131782153 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2408+3823G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782153 | |||||||
chr12:131782218 | T | C | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2408+3888T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782218 | |||||||
chr12:131782472 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2409-3991C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782472 | |||||||
chr12:131782511 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
7 | HG02027.hp2 NA18939.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-3952T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782511 | |||||||
chr12:131782512 | T | C | 2 | a0001c0001t0001g0182 a0014c0030t0001g0189 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2409-3951T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782512 | |||||||
chr12:131782665 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2409-3798A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782665 | |||||||
chr12:131782699 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2409-3764C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782699 | |||||||
chr12:131782948 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2409-3515A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782948 | |||||||
chr12:131783016 | A | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2409-3447A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783016 | |||||||
chr12:131783074 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-3389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783074 | |||||||
chr12:131783179 | T | TA | 36 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0083 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2409-3265dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783179 | ||||||
chr12:131783179 | TA | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0127 others(6): Show |
9 | HG01496.hp1 HG01975.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2409-3265delA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783179 | ||||||
chr12:131783289 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2409-3174T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783289 | |||||||
chr12:131783476 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2409-2987A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783476 | |||||||
chr12:131783518 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2945G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783518 | |||||||
chr12:131783530 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2409-2933G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783530 | |||||||
chr12:131783696 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2409-2767G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783696 | |||||||
chr12:131783728 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2409-2735A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783728 | |||||||
chr12:131783734 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
21 | HG00558.hp2 HG02015.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2409-2729G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783734 | |||||||
chr12:131783774 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2409-2689G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783774 | |||||||
chr12:131783792 | T | TATATATA others(24): Show |
1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2409-2671_2409-267 others(35): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783792 | |||||||
chr12:131783792 | T | TATATATA others(28): Show |
1 | a0001c0001t0001g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2409-2671_2409-267 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783792 | |||||||
chr12:131783792 | T | TTA | 6 | a0001c0001t0001g0012 a0001c0001t0003g0036 a0001c0001t0003g0037 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2409-2642_2409-264 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATA | 5 | a0001c0001t0001g0105 a0001c0001t0002g0019 a0001c0004t0001g0099 others(2): Show |
5 | HG01934.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2644_2409-264 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATA | 4 | a0001c0001t0001g0013 a0001c0001t0001g0145 a0001c0001t0001g0158 others(1): Show |
4 | HG01243.hp1 NA18941.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-2646_2409-264 others(10): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(3): Show |
5 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0227 others(2): Show |
5 | HG00558.hp1 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2650_2409-264 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(5): Show |
7 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0215 others(4): Show |
7 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2652_2409-264 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(7): Show |
9 | a0001c0001t0001g0047 a0001c0001t0001g0107 a0001c0001t0001g0208 others(6): Show |
9 | HG00140.hp2 HG01952.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.2409-2654_2409-264 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(9): Show |
8 | a0001c0001t0001g0207 a0001c0001t0001g0220 a0001c0001t0001g0271 others(5): Show |
8 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2409-2656_2409-264 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(11): Show |
7 | a0001c0001t0001g0176 a0001c0001t0001g0200 a0001c0002t0001g0294 others(4): Show |
7 | HG00741.hp1 HG01099.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2658_2409-264 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(13): Show |
6 | a0001c0001t0001g0073 a0001c0001t0001g0179 a0001c0001t0001g0212 others(3): Show |
6 | HG00140.hp1 HG01243.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.2409-2660_2409-264 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(15): Show |
5 | a0001c0001t0001g0140 a0001c0002t0001g0283 a0001c0002t0001g0288 others(2): Show |
5 | HG00673.hp2 HG01071.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-2662_2409-264 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(17): Show |
5 | a0001c0001t0001g0110 a0001c0001t0001g0230 a0001c0001t0001g0281 others(2): Show |
5 | HG00639.hp2 HG02040.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-2664_2409-264 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(19): Show |
5 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0228 others(2): Show |
5 | HG01517.hp2 HG02148.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2666_2409-264 others(30): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(21): Show |
5 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG00099.hp2 HG02071.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2668_2409-264 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(23): Show |
8 | a0001c0001t0001g0130 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
8 | HG02293.hp2 HG02698.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2409-2670_2409-264 others(34): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(25): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0001g0116 others(11): Show |
15 | HG00738.hp2 HG01069.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(27): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0106 others(10): Show |
13 | HG00735.hp2 HG01168.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(38): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(29): Show |
15 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0072 others(12): Show |
15 | HG01123.hp1 HG01975.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(40): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(31): Show |
5 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0002t0001g0297 others(2): Show |
5 | HG01517.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(42): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(33): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0144 others(1): Show |
4 | HG02129.hp1 HG02132.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(44): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(35): Show |
1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(46): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(37): Show |
3 | a0001c0001t0001g0068 a0001c0001t0001g0159 a0001c0001t0001g0171 |
3 | HG00280.hp2 HG01261.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(48): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(41): Show |
1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(43): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0067 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(54): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(49): Show |
1 | a0003c0005t0001g0121 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(60): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATATAT others(17): Show |
1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2409-2652_2409-265 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTATTATA others(38): Show |
1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2409-2668_2409-266 others(49): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTATAT others(17): Show |
1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTATAT others(21): Show |
2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01167.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2409-2670_2409-266 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTATAT others(25): Show |
1 | a0001c0001t0001g0277 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTATAT others(29): Show |
1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(40): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTATAT others(41): Show |
1 | a0001c0001t0001g0269 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | T | TTTTTTAT others(25): Show |
1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | TTA | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
99 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.2409-2642_2409-264 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | TTATA | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0175 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.2409-2644_2409-264 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | TTATATA | T | 8 | a0001c0001t0001g0150 a0001c0006t0001g0014 a0001c0006t0001g0015 others(5): Show |
8 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2409-2646_2409-264 others(10): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783792 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2409-2650_2409-264 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | ||||||
chr12:131783821 | T | TATATATA others(5): Show |
2 | a0001c0008t0001g0235 a0001c0008t0001g0236 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | ||||||
chr12:131783821 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(46): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | ||||||
chr12:131783821 | T | TATATATA others(41): Show |
1 | a0001c0001t0001g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | ||||||
chr12:131783821 | T | TATATATA others(43): Show |
1 | a0001c0001t0001g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(54): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | ||||||
chr12:131783849 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2409-2614A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783849 | |||||||
chr12:131783967 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2409-2496T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783967 | |||||||
chr12:131784011 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2409-2452G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784011 | |||||||
chr12:131784013 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-2450A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784013 | |||||||
chr12:131784231 | T | TG | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0002g0019 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2409-2229dupG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131784231 | ||||||
chr12:131784244 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2409-2219G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784244 | |||||||
chr12:131784273 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2409-2190C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784273 | |||||||
chr12:131784299 | A | C | 49 | a0001c0001t0001g0107 a0001c0001t0001g0175 a0001c0001t0001g0176 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.2409-2164A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784299 | |||||||
chr12:131784377 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2409-2086C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784377 | |||||||
chr12:131784416 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2409-2047T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784416 | |||||||
chr12:131784670 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2409-1793G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784670 | |||||||
chr12:131784954 | C | T | 5 | a0001c0001t0003g0018 a0001c0001t0003g0025 a0001c0001t0003g0031 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-1509C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784954 | |||||||
chr12:131785099 | G | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2409-1364G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785099 | |||||||
chr12:131785235 | AACTG | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2409-1225_2409-122 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131785235 | ||||||
chr12:131785285 | G | GA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2409-1172dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131785285 | ||||||
chr12:131785770 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2409-693G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785770 | |||||||
chr12:131785913 | T | C | 49 | a0001c0001t0001g0107 a0001c0001t0001g0175 a0001c0001t0001g0176 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.2409-550T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785913 | |||||||
chr12:131785941 | C | A | 1 | a0001c0019t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2409-522C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785941 | |||||||
chr12:131786021 | G | A | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2409-442G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786021 | |||||||
chr12:131786199 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2409-264G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786199 | |||||||
chr12:131786221 | G | A | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-242G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786221 | |||||||
chr12:131786238 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-225G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786238 | |||||||
chr12:131786304 | A | T | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2409-159A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786304 | |||||||
chr12:131786680 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0260 |
2 | HG00558.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2534+92G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786680 | |||||||
chr12:131786718 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2534+130A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786718 | |||||||
chr12:131786790 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+202G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786790 | |||||||
chr12:131786819 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0003g0037 |
3 | HG03490.hp2 HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2534+231C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786819 | |||||||
chr12:131787118 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2534+530G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787118 | |||||||
chr12:131787276 | A | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2534+688A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787276 | |||||||
chr12:131787300 | AC | A | 60 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(57): Show |
61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2534+716delC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131787300 | ||||||
chr12:131787312 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0133 others(1): Show |
4 | NA18979.hp2 NA18986.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2534+724A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787312 | |||||||
chr12:131787469 | G | C | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+881G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787469 | |||||||
chr12:131787573 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2534+985T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787573 | |||||||
chr12:131787680 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2534+1092A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787680 | |||||||
chr12:131787871 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.2534+1283C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787871 | |||||||
chr12:131787874 | A | T | 1 | a0001c0001t0005g0222 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2534+1286A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787874 | |||||||
chr12:131788033 | C | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2534+1445C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788033 | |||||||
chr12:131788180 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
60 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.2534+1592T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788180 | |||||||
chr12:131788253 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2534+1665C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788253 | |||||||
chr12:131788277 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0005g0222 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2534+1689C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788277 | |||||||
chr12:131788282 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2534+1694A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788282 | |||||||
chr12:131788531 | G | GT | 26 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0122 others(23): Show |
26 | HG01074.hp2 HG01496.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2534+1955dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131788531 | ||||||
chr12:131788771 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2534+2183A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788771 | |||||||
chr12:131788819 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2534+2231C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788819 | |||||||
chr12:131788862 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+2274T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788862 | |||||||
chr12:131788922 | G | A | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2534+2334G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788922 | |||||||
chr12:131788988 | A | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2534+2400A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788988 | |||||||
chr12:131789156 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+2568A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789156 | |||||||
chr12:131789236 | C | T | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2534+2648C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789236 | |||||||
chr12:131789362 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2534+2774A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789362 | |||||||
chr12:131789373 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+2785A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789373 | |||||||
chr12:131789403 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2534+2815A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789403 | |||||||
chr12:131789590 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+3002C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789590 | |||||||
chr12:131789723 | A | C | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2534+3135A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789723 | |||||||
chr12:131789811 | G | A | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0208 others(6): Show |
9 | HG00558.hp1 HG00609.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.2534+3223G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789811 | |||||||
chr12:131789969 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0308 a0007c0021t0003g0020 |
3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2534+3381G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789969 | |||||||
chr12:131790001 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+3413A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790001 | |||||||
chr12:131790103 | C | A | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2534+3515C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790103 | |||||||
chr12:131790203 | T | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2534+3615T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790203 | |||||||
chr12:131790417 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2534+3829G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790417 | |||||||
chr12:131790540 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2534+3952C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790540 | |||||||
chr12:131790738 | G | A | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2534+4150G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790738 | |||||||
chr12:131790755 | G | A | 111 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0047 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.2534+4167G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790755 | |||||||
chr12:131790811 | A | G | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2534+4223A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790811 | |||||||
chr12:131790845 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2534+4257G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790845 | |||||||
chr12:131790916 | T | C | 1 | a0002c0003t0003g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2534+4328T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790916 | |||||||
chr12:131790985 | C | A | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2534+4397C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790985 | |||||||
chr12:131791042 | A | G | 87 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(84): Show |
88 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.2534+4454A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791042 | |||||||
chr12:131791085 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2534+4497G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791085 | |||||||
chr12:131791120 | C | T | 60 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(57): Show |
61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2534+4532C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791120 | |||||||
chr12:131791159 | A | G | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0002g0019 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2534+4571A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791159 | |||||||
chr12:131791220 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
70 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.2534+4632C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791220 | |||||||
chr12:131791225 | A | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
71 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.2534+4637A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791225 | |||||||
chr12:131791273 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+4685C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791273 | |||||||
chr12:131791593 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2534+5005G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791593 | |||||||
chr12:131791625 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2534+5037G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791625 | |||||||
chr12:131791778 | T | C | 2 | a0001c0001t0001g0182 a0014c0030t0001g0189 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2534+5190T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791778 | |||||||
chr12:131791779 | T | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2534+5191T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791779 | |||||||
chr12:131791952 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2535-5226G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791952 | |||||||
chr12:131792026 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2535-5152T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792026 | |||||||
chr12:131792026 | TCGTGTGT others(28): Show |
T | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2535-5132_2535-509 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792026 | ||||||
chr12:131792028 | GTGTGTGT others(63): Show |
G | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2535-5098_2535-502 others(74): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792028 | ||||||
chr12:131792040 | G | A | 5 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2535-5138G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792040 | |||||||
chr12:131792094 | G | A | 2 | a0001c0004t0001g0099 a0004c0009t0001g0053 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2535-5084G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792094 | |||||||
chr12:131792098 | A | G | 2 | a0001c0004t0002g0306 a0001c0004t0002g0307 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2535-5080A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792098 | |||||||
chr12:131792116 | GTACTGTG others(98): Show |
G | 4 | a0001c0006t0001g0014 a0001c0006t0001g0015 a0001c0006t0001g0017 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535-5050_2535-494 others(4): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792116 | ||||||
chr12:131792133 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2535-5045G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792133 | |||||||
chr12:131792144 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2535-5034C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792144 | |||||||
chr12:131792154 | C | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0308 a0007c0021t0003g0020 |
3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2535-5024C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792154 | |||||||
chr12:131792253 | CCAGTACT others(28): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2535-4908_2535-487 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792253 | ||||||
chr12:131792279 | A | ATTCACAG others(165): Show |
2 | a0001c0002t0001g0294 a0001c0002t0001g0298 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2535-4836_2535-466 others(176): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792279 | ||||||
chr12:131792289 | C | T | 3 | a0004c0009t0001g0052 a0004c0009t0001g0053 a0008c0023t0001g0051 |
3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2535-4889C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792289 | |||||||
chr12:131792342 | TGTGTGTG others(28): Show |
T | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2535-4811_2535-477 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792342 | ||||||
chr12:131792417 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2535-4761C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792417 | |||||||
chr12:131792433 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-4745G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792433 | |||||||
chr12:131792451 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2535-4727G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792451 | |||||||
chr12:131792514 | C | T | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2535-4664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792514 | |||||||
chr12:131792546 | G | A | 20 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(17): Show |
20 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.2535-4632G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792546 | |||||||
chr12:131792584 | G | A | 23 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0025 others(20): Show |
24 | HG01934.hp2 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2535-4594G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792584 | |||||||
chr12:131792611 | ACATGTGT others(27): Show |
A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-4550_2535-451 others(38): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792611 | ||||||
chr12:131792658 | C | T | 1 | a0001c0006t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2535-4520C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792658 | |||||||
chr12:131792680 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(77): Show |
81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2535-4498A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792680 | |||||||
chr12:131792789 | G | A | 1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2535-4389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792789 | |||||||
chr12:131792889 | C | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-4289C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792889 | |||||||
chr12:131793057 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0270 |
2 | HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2535-4121A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793057 | |||||||
chr12:131793092 | C | A | 3 | a0001c0004t0002g0009 a0001c0004t0002g0010 a0001c0004t0002g0011 |
3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2535-4086C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793092 | |||||||
chr12:131793134 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2535-4044T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793134 | |||||||
chr12:131793165 | G | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-4013G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793165 | |||||||
chr12:131793169 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2535-4009G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793169 | |||||||
chr12:131793319 | A | G | 32 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(29): Show |
32 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.2535-3859A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793319 | |||||||
chr12:131793330 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0180 a0001c0001t0001g0255 |
4 | HG02040.hp1 HG02132.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2535-3848T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793330 | |||||||
chr12:131793644 | G | A | 1 | a0002c0003t0004g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2535-3534G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793644 | |||||||
chr12:131793647 | A | G | 62 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(59): Show |
63 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.2535-3531A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793647 | |||||||
chr12:131793716 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-3462T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793716 | |||||||
chr12:131793852 | C | A | 60 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(57): Show |
61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2535-3326C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793852 | |||||||
chr12:131793860 | G | A | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-3318G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793860 | |||||||
chr12:131793910 | G | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2535-3268G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793910 | |||||||
chr12:131793940 | C | T | 3 | a0001c0001t0001g0200 a0001c0008t0001g0235 a0001c0008t0001g0236 |
3 | HG00733.hp2 HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2535-3238C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793940 | |||||||
chr12:131793948 | G | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2535-3230G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793948 | |||||||
chr12:131793981 | T | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0308 a0007c0021t0003g0020 |
3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2535-3197T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793981 | |||||||
chr12:131793985 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2535-3193G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793985 | |||||||
chr12:131794021 | T | G | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2535-3157T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794021 | |||||||
chr12:131794164 | A | G | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-3014A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794164 | |||||||
chr12:131794374 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2535-2804A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794374 | |||||||
chr12:131794695 | C | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-2483C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794695 | |||||||
chr12:131794787 | G | A | 61 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(58): Show |
62 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.2535-2391G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794787 | |||||||
chr12:131794797 | A | G | 62 | a0001c0001t0001g0061 a0001c0001t0002g0050 a0001c0001t0002g0054 others(59): Show |
63 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.2535-2381A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794797 | |||||||
chr12:131795067 | A | G | 2 | a0001c0008t0001g0235 a0001c0008t0001g0236 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2535-2111A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795067 | |||||||
chr12:131795412 | G | A | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1766G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795412 | |||||||
chr12:131795482 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2535-1696A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795482 | |||||||
chr12:131795539 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2535-1639C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795539 | |||||||
chr12:131795664 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1514C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795664 | |||||||
chr12:131795721 | G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2535-1457G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795721 | |||||||
chr12:131795885 | C | T | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2535-1293C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795885 | |||||||
chr12:131795929 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2535-1249T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795929 | |||||||
chr12:131795964 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2535-1214C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795964 | |||||||
chr12:131795964 | CGGGAGGG others(9): Show |
C | 1 | a0001c0002t0001g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2535-1201_2535-118 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795964 | ||||||
chr12:131795964 | CGGGAGGG others(32): Show |
C | 1 | a0001c0001t0003g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2535-1201_2535-116 others(43): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795964 | ||||||
chr12:131795971 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2535-1207G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795971 | |||||||
chr12:131795978 | T | TAGGGGAG others(16): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0173 |
2 | HG01168.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2535-1159_2535-113 others(27): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795978 | ||||||
chr12:131795979 | AGGGGAGG others(11): Show |
A | 1 | a0001c0001t0002g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2535-1182_2535-116 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795979 | ||||||
chr12:131795979 | AGGGGAGG others(34): Show |
A | 2 | a0001c0001t0001g0221 a0001c0001t0005g0222 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2535-1182_2535-114 others(45): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795979 | ||||||
chr12:131795991 | GGGAGAGG others(44): Show |
G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2535-1162_2535-111 others(55): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795991 | ||||||
chr12:131795995 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-1183G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795995 | |||||||
chr12:131795995 | GAGGGGGA others(15): Show |
G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1182_2535-116 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795995 | |||||||
chr12:131795997 | G | GGGGGAGG others(39): Show |
2 | a0001c0001t0001g0279 a0006c0020t0001g0280 |
2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2535-1165_2535-116 others(50): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795997 | G | GGGGGAGG others(21): Show |
60 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(57): Show |
61 | HG00597.hp1 HG00609.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.2535-1164_2535-113 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795997 | G | GGGGGAGG others(22): Show |
1 | a0001c0001t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2535-1160_2535-115 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795997 | G | GGGGGGAG others(22): Show |
1 | a0012c0024t0001g0131 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2535-1177_2535-117 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795997 | GGGGGA | G | 20 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(17): Show |
20 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.2535-1164_2535-116 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795997 | GGGGGAGG others(15): Show |
G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0261 a0001c0001t0002g0282 |
3 | HG01099.hp1 HG02071.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2535-1176_2535-115 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | ||||||
chr12:131795998 | G | A | 1 | a0003c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-1180G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795998 | |||||||
chr12:131796014 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2535-1164G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796014 | |||||||
chr12:131796017 | A | AGAGGGGG others(23): Show |
1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(34): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796017 | ||||||
chr12:131796018 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2535-1160G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796018 | |||||||
chr12:131796019 | A | AGGGGGAG others(22): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0165 |
3 | HG00673.hp2 HG02056.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2535-1137_2535-113 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796019 | ||||||
chr12:131796019 | A | G | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1159A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796019 | |||||||
chr12:131796019 | AGGGGGAG others(16): Show |
A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2535-1156_2535-113 others(27): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796019 | ||||||
chr12:131796020 | G | GGGGGAGG others(20): Show |
1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(31): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796020 | ||||||
chr12:131796020 | GGGGGA | G | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-1141_2535-113 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796020 | ||||||
chr12:131796022 | G | A | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1156G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796022 | |||||||
chr12:131796024 | G | A | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1154G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796024 | |||||||
chr12:131796025 | A | AGGGGAGG others(22): Show |
1 | a0003c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796025 | ||||||
chr12:131796025 | A | AGGGGAGG others(39): Show |
4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0142 others(1): Show |
4 | NA18995.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535-1137_2535-113 others(50): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796025 | ||||||
chr12:131796025 | A | G | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1153A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796025 | |||||||
chr12:131796027 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-1151G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796027 | |||||||
chr12:131796027 | G | GGGAGGGG others(25): Show |
1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2535-1144_2535-114 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796027 | ||||||
chr12:131796042 | C | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.2535-1136C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796042 | |||||||
chr12:131796042 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0154 |
3 | HG03927.hp2 NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2535-1136C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796042 | |||||||
chr12:131796047 | A | AGGGGGAG others(22): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0154 |
2 | HG03927.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2535-1112_2535-111 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796047 | ||||||
chr12:131796047 | A | AGGGGGAG others(25): Show |
1 | a0001c0001t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2535-1116_2535-111 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796047 | ||||||
chr12:131796047 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-1131A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796047 | |||||||
chr12:131796136 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2535-1042A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796136 | |||||||
chr12:131796160 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0186 |
3 | HG01243.hp1 HG03098.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2535-1018G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796160 | |||||||
chr12:131796264 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-914G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796264 | |||||||
chr12:131796597 | A | ACAACAGA others(7): Show |
1 | a0003c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-579_2535-566d others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796597 | ||||||
chr12:131796608 | A | C | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-570A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796608 | |||||||
chr12:131796610 | A | C | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-568A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796610 | |||||||
chr12:131796717 | G | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0054 a0001c0001t0002g0058 |
3 | HG02027.hp1 NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2535-461G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796717 | |||||||
chr12:131796778 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-400C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796778 | |||||||
chr12:131796962 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2535-216A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796962 | |||||||
chr12:131797006 | A | G | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2535-172A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131797006 | |||||||
chr12:131797020 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-158A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131797020 | |||||||
chr12:131797511 | G | A | 2 | a0001c0008t0001g0235 a0001c0008t0001g0236 |
2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2717+151G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797511 | |||||||
chr12:131797535 | C | T | 59 | a0001c0001t0002g0050 a0001c0001t0002g0054 a0001c0001t0002g0055 others(56): Show |
60 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.2717+175C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797535 | |||||||
chr12:131797537 | C | A | 23 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0001g0285 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2717+177C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797537 | |||||||
chr12:131797547 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2717+187G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797547 | |||||||
chr12:131797571 | C | G | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2717+211C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797571 | |||||||
chr12:131797957 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2717+597G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797957 | |||||||
chr12:131797967 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2717+607G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797967 | |||||||
chr12:131798079 | A | G | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2717+719A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798079 | |||||||
chr12:131798135 | A | G | 1 | a0001c0018t0001g0016 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2717+775A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798135 | |||||||
chr12:131798276 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2718-761C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798276 | |||||||
chr12:131798316 | A | G | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2718-721A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798316 | |||||||
chr12:131798406 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2718-631G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798406 | |||||||
chr12:131798449 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2718-588C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798449 | |||||||
chr12:131798460 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2718-577G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798460 | |||||||
chr12:131798616 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2718-421G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798616 | |||||||
chr12:131798696 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2718-341C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798696 | |||||||
chr12:131798746 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2718-291C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798746 | |||||||
chr12:131798845 | G | A | 6 | a0001c0001t0002g0084 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | HG02145.hp1 HG02895.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2718-192G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798845 | |||||||
chr12:131798975 | A | G | 7 | a0001c0001t0002g0019 a0001c0004t0002g0009 a0001c0004t0002g0010 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2718-62A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798975 | |||||||
chr12:131799246 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2790+137G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799246 | |||||||
chr12:131799256 | G | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2790+147G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799256 | |||||||
chr12:131799313 | G | A | 59 | a0001c0001t0002g0050 a0001c0001t0002g0054 a0001c0001t0002g0055 others(56): Show |
60 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.2791-110G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799313 | |||||||
chr12:131799327 | C | CTT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0002g0019 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2791-95_2791-94ins others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 131799327 | ||||||
chr12:131799346 | C | T | 2 | a0001c0012t0001g0044 a0001c0012t0001g0045 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2791-77C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799346 | |||||||
chr12:131799380 | G | A | 1 | a0010c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2791-43G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799380 | |||||||
chr12:131799413 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2791-10C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799413 |