Item | Value |
---|---|
geneid | 124989 |
ensemblid | ENSG00000178852.16 |
hgncid | 26864 |
symbol | EFCAB13 |
name | EF-hand calcium binding domain 13 |
refseq_nuc | NM_152347.5 |
refseq_prot | NP_689560.3 |
ensembl_nuc | ENST00000331493.7 |
ensembl_prot | ENSP00000332111.2 |
mane_status | MANE Select |
chr | chr17 |
start | 47323955 |
end | 47441312 |
strand | + |
ver | v1.2 |
region | chr17:47323955-47441312 |
region5000 | chr17:47318955-47446312 |
regionname0 | EFCAB13_chr17_47323955_47441312 |
regionname5000 | EFCAB13_chr17_47318955_47446312 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 281 | 138 | 36 | 30 | 48 | 6 | 17 | 41 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(276): Show |
chr17 | 47318955 | 47446312 |
a0002 | 1/0 | 973 | 82 | 21 | 16 | 31 | 4 | 9 | 24 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0003 | 0/0 | 973 | 39 | 7 | 4 | 27 | 1 | 0 | 23 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0004 | 0/0 | 973 | 38 | 3 | 7 | 22 | 1 | 5 | 18 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0005 | 0/0 | 210 | 27 | 0 | 1 | 20 | 0 | 6 | 13 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(205): Show |
chr17 | 47318955 | 47446312 |
a0006 | 0/0 | 973 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0007 | 0/0 | 973 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0008 | 0/0 | 973 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0009 | 0/0 | 973 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0010 | 0/0 | 973 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0011 | 0/0 | 210 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(205): Show |
chr17 | 47318955 | 47446312 |
a0012 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0013 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0014 | 0/0 | 973 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0015 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0016 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(968): Show |
chr17 | 47318955 | 47446312 |
a0017 | 0/0 | 281 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | METKV others(276): Show |
chr17 | 47318955 | 47446312 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2918 | 116 | 34 | 19 | 44 | 4 | 15 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0006 | 0/0 | 2918 | 13 | 2 | 8 | 0 | 2 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0013 | 0/1 | 2918 | 3 | 0 | 2 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0015 | 0/0 | 2918 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0022 | 0/0 | 2918 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0023 | 0/0 | 2918 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0024 | 0/0 | 2918 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0001c0025 | 0/0 | 2918 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 | ||
a0002c0002 | 1/0 | 2919 | 76 | 15 | 16 | 31 | 4 | 9 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0002c0010 | 0/0 | 2919 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0003c0004 | 0/0 | 2919 | 29 | 2 | 0 | 26 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0003c0008 | 0/0 | 2919 | 9 | 5 | 3 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0003c0016 | 0/0 | 2919 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0004c0003 | 0/0 | 2919 | 38 | 3 | 7 | 22 | 1 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0005c0005 | 0/0 | 2919 | 27 | 0 | 1 | 20 | 0 | 6 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0006c0007 | 0/0 | 2919 | 9 | 0 | 0 | 9 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0007c0009 | 0/0 | 2919 | 6 | 0 | 0 | 6 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0008c0011 | 0/0 | 2919 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0009c0012 | 0/0 | 2919 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0010c0014 | 0/0 | 2919 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0011c0027 | 0/0 | 2919 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0012c0019 | 0/0 | 2919 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0013c0017 | 0/0 | 2919 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0014c0018 | 0/0 | 2919 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0015c0021 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0016c0020 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2914): Show |
chr17 | 47318955 | 47446312 | ||
a0017c0026 | 0/0 | 2918 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | ATGGA others(2913): Show |
chr17 | 47318955 | 47446312 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3956 | 111 | 31 | 19 | 42 | 4 | 15 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0001t0002 | 0/0 | 3956 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0001t0005 | 0/0 | 3956 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0006t0001 | 0/0 | 3956 | 6 | 0 | 4 | 0 | 1 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0006t0002 | 0/0 | 3956 | 5 | 1 | 3 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0006t0003 | 0/0 | 3956 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0013t0001 | 0/1 | 3956 | 3 | 0 | 2 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0015t0001 | 0/0 | 3956 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0022t0001 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0023t0002 | 0/0 | 3956 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0024t0001 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0001c0025t0001 | 0/0 | 3956 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
a0002c0002t0001 | 1/0 | 3957 | 62 | 13 | 10 | 30 | 3 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0002c0002t0003 | 0/0 | 3957 | 12 | 2 | 6 | 0 | 1 | 3 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0002c0002t0008 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0002c0002t0009 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0002c0010t0001 | 0/0 | 3957 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0004t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0004t0002 | 0/0 | 3957 | 28 | 1 | 0 | 26 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0008t0001 | 0/0 | 3957 | 2 | 0 | 1 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0008t0003 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0008t0004 | 0/0 | 3957 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0003c0016t0002 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0004c0003t0001 | 0/0 | 3957 | 37 | 2 | 7 | 22 | 1 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0004c0003t0006 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0005c0005t0001 | 0/0 | 3957 | 23 | 0 | 0 | 19 | 0 | 4 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0005c0005t0002 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0005c0005t0003 | 0/0 | 3957 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0005c0005t0007 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0006c0007t0001 | 0/0 | 3957 | 8 | 0 | 0 | 8 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0006c0007t0010 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0007c0009t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0007c0009t0002 | 0/0 | 3957 | 5 | 0 | 0 | 5 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0008c0011t0001 | 0/0 | 3957 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0009c0012t0002 | 0/0 | 3957 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0010c0014t0001 | 0/0 | 3957 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0011c0027t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0012c0019t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0013c0017t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0014c0018t0001 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0015c0021t0006 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0016c0020t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3952): Show |
chr17 | 47318955 | 47446312 |
a0017c0026t0001 | 0/0 | 3956 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | GCGGC others(3951): Show |
chr17 | 47318955 | 47446312 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0006t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0013t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0013t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0013t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0015t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0022t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0023t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0024t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0001c0025t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0008g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0002t0009g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0002c0010t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0008t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0003c0016t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0004c0003t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0005c0005t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0006c0007t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0007c0009t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0008c0011t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0008c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0008c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0008c0011t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0009c0012t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0009c0012t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0009c0012t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0010c0014t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0010c0014t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0011c0027t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0012c0019t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0013c0017t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0014c0018t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0015c0021t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0016c0020t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
a0017c0026t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0006 | t0001 | g0095 | EUR | GBR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0316 | EUR | GBR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00280 | hp2 | a0004 | c0003 | t0001 | g0038 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00323 | hp2 | a0002 | c0002 | t0003 | g0315 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00408 | hp1 | a0006 | c0007 | t0001 | g0062 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00408 | hp2 | a0005 | c0005 | t0001 | g0074 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00423 | hp1 | a0005 | c0005 | t0001 | g0071 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00423 | hp2 | a0006 | c0007 | t0001 | g0340 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00438 | hp1 | a0005 | c0005 | t0001 | g0008 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00438 | hp2 | a0003 | c0004 | t0002 | g0244 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00544 | hp1 | a0003 | c0004 | t0002 | g0228 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00544 | hp2 | a0005 | c0005 | t0001 | g0211 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00558 | hp1 | a0007 | c0009 | t0002 | g0218 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00558 | hp2 | a0005 | c0005 | t0001 | g0068 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00642 | hp1 | a0001 | c0006 | t0003 | g0096 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00735 | hp1 | a0001 | c0006 | t0001 | g0097 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00738 | hp1 | a0004 | c0003 | t0001 | g0020 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0284 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0338 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01070 | hp1 | a0001 | c0013 | t0001 | g0196 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01071 | hp1 | a0001 | c0013 | t0001 | g0197 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0324 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01081 | hp1 | a0001 | c0006 | t0002 | g0102 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01099 | hp1 | a0001 | c0025 | t0001 | g0144 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01099 | hp2 | a0001 | c0006 | t0001 | g0098 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01106 | hp1 | a0003 | c0008 | t0004 | g0012 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0320 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01109 | hp1 | a0004 | c0003 | t0001 | g0022 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01168 | hp1 | a0001 | c0006 | t0001 | g0093 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01169 | hp1 | a0001 | c0006 | t0001 | g0094 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01175 | hp1 | a0001 | c0006 | t0002 | g0099 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01243 | hp2 | a0003 | c0008 | t0001 | g0006 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0057 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01256 | hp1 | a0002 | c0002 | t0003 | g0336 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01261 | hp1 | a0004 | c0003 | t0001 | g0021 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01261 | hp2 | a0001 | c0006 | t0002 | g0073 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01346 | hp1 | a0004 | c0003 | t0001 | g0003 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01346 | hp2 | a0003 | c0016 | t0002 | g0223 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01358 | hp1 | a0004 | c0003 | t0001 | g0033 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0318 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01433 | hp2 | a0012 | c0019 | t0001 | g0280 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0319 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0281 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01515 | hp2 | a0003 | c0004 | t0002 | g0245 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0282 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0331 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01975 | hp1 | a0004 | c0003 | t0001 | g0023 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01993 | hp2 | a0004 | c0003 | t0001 | g0034 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02004 | hp2 | a0005 | c0005 | t0003 | g0117 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02015 | hp2 | a0004 | c0003 | t0001 | g0047 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02027 | hp1 | a0001 | c0022 | t0001 | g0194 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02027 | hp2 | a0005 | c0005 | t0001 | g0115 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02055 | hp1 | a0001 | c0006 | t0002 | g0072 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02056 | hp1 | a0004 | c0003 | t0001 | g0046 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02056 | hp2 | a0013 | c0017 | t0001 | g0209 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02083 | hp1 | a0004 | c0003 | t0001 | g0045 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02135 | hp2 | a0006 | c0007 | t0001 | g0060 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02148 | hp1 | a0003 | c0008 | t0003 | g0276 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02155 | hp2 | a0005 | c0005 | t0001 | g0206 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02523 | hp1 | a0004 | c0003 | t0001 | g0032 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0335 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02602 | hp1 | a0001 | c0006 | t0001 | g0100 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02602 | hp2 | a0005 | c0005 | t0001 | g0069 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02615 | hp1 | a0002 | c0010 | t0001 | g0267 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02647 | hp2 | a0008 | c0011 | t0001 | g0049 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0328 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02717 | hp2 | a0002 | c0010 | t0001 | g0265 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02735 | hp2 | a0004 | c0003 | t0001 | g0044 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02738 | hp2 | a0005 | c0005 | t0001 | g0274 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02809 | hp2 | a0003 | c0008 | t0004 | g0053 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02818 | hp1 | a0001 | c0006 | t0003 | g0101 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0350 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02965 | hp1 | a0003 | c0004 | t0001 | g0141 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02976 | hp2 | a0008 | c0011 | t0001 | g0050 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03017 | hp1 | a0014 | c0018 | t0001 | g0337 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0347 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03041 | hp2 | a0003 | c0008 | t0004 | g0011 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03130 | hp1 | a0015 | c0021 | t0006 | g0261 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03139 | hp2 | a0002 | c0010 | t0001 | g0269 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0326 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03486 | hp1 | a0008 | c0011 | t0001 | g0054 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03492 | hp2 | a0004 | c0003 | t0001 | g0035 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0348 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0349 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03654 | hp1 | a0005 | c0005 | t0003 | g0327 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03669 | hp1 | a0002 | c0002 | t0008 | g0323 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03688 | hp1 | a0004 | c0003 | t0001 | g0039 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03704 | hp2 | a0005 | c0005 | t0007 | g0213 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03710 | hp2 | a0004 | c0003 | t0001 | g0036 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03834 | hp1 | a0005 | c0005 | t0001 | g0204 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03834 | hp2 | a0004 | c0003 | t0001 | g0037 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03927 | hp2 | a0005 | c0005 | t0001 | g0075 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0291 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0058 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04228 | hp1 | a0001 | c0023 | t0002 | g0229 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0301 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18522 | hp1 | a0003 | c0008 | t0004 | g0005 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18612 | hp1 | a0003 | c0004 | t0002 | g0232 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18747 | hp1 | a0003 | c0004 | t0002 | g0219 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18906 | hp1 | a0008 | c0011 | t0001 | g0273 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18906 | hp2 | a0003 | c0008 | t0004 | g0157 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18941 | hp2 | a0009 | c0012 | t0002 | g0215 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18942 | hp1 | a0003 | c0004 | t0002 | g0233 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18943 | hp2 | a0003 | c0004 | t0002 | g0250 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18944 | hp2 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18945 | hp1 | a0003 | c0004 | t0002 | g0226 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18946 | hp1 | a0003 | c0004 | t0002 | g0222 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18948 | hp1 | a0003 | c0004 | t0002 | g0231 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18952 | hp1 | a0003 | c0004 | t0002 | g0240 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18956 | hp1 | a0004 | c0003 | t0001 | g0030 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18957 | hp1 | a0005 | c0005 | t0001 | g0342 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18961 | hp2 | a0007 | c0009 | t0002 | g0252 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18963 | hp1 | a0006 | c0007 | t0001 | g0059 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18963 | hp2 | a0004 | c0003 | t0001 | g0027 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0251 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18964 | hp2 | a0004 | c0003 | t0001 | g0025 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18965 | hp1 | a0005 | c0005 | t0001 | g0201 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18965 | hp2 | a0006 | c0007 | t0001 | g0339 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18969 | hp2 | a0009 | c0012 | t0002 | g0004 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18971 | hp1 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18974 | hp2 | a0004 | c0003 | t0001 | g0026 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18975 | hp1 | a0007 | c0009 | t0002 | g0248 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18975 | hp2 | a0004 | c0003 | t0001 | g0024 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18977 | hp2 | a0005 | c0005 | t0001 | g0212 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18979 | hp2 | a0004 | c0003 | t0001 | g0029 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18981 | hp1 | a0001 | c0015 | t0001 | g0192 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18981 | hp2 | a0005 | c0005 | t0001 | g0207 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18982 | hp2 | a0010 | c0014 | t0001 | g0288 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18983 | hp2 | a0003 | c0004 | t0002 | g0243 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18984 | hp1 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18984 | hp2 | a0003 | c0004 | t0002 | g0227 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18985 | hp1 | a0004 | c0003 | t0001 | g0067 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18985 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18988 | hp1 | a0007 | c0009 | t0001 | g0221 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18990 | hp1 | a0003 | c0004 | t0002 | g0237 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18993 | hp2 | a0009 | c0012 | t0002 | g0004 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18997 | hp1 | a0006 | c0007 | t0010 | g0061 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18998 | hp1 | a0004 | c0003 | t0001 | g0066 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18998 | hp2 | a0003 | c0008 | t0001 | g0134 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18999 | hp1 | a0004 | c0003 | t0001 | g0028 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19000 | hp1 | a0005 | c0005 | t0001 | g0116 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19000 | hp2 | a0007 | c0009 | t0002 | g0247 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19003 | hp1 | a0003 | c0004 | t0002 | g0234 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19003 | hp2 | a0005 | c0005 | t0001 | g0208 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19004 | hp1 | a0005 | c0005 | t0001 | g0202 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19004 | hp2 | a0003 | c0004 | t0002 | g0216 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19005 | hp2 | a0006 | c0007 | t0001 | g0063 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19007 | hp1 | a0001 | c0024 | t0001 | g0191 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19007 | hp2 | a0005 | c0005 | t0001 | g0110 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19009 | hp2 | a0003 | c0004 | t0002 | g0253 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19010 | hp1 | a0004 | c0003 | t0001 | g0048 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19011 | hp2 | a0003 | c0004 | t0002 | g0249 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19030 | hp1 | a0004 | c0003 | t0006 | g0260 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19055 | hp1 | a0003 | c0004 | t0002 | g0220 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19055 | hp2 | a0001 | c0015 | t0001 | g0106 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19056 | hp1 | a0003 | c0004 | t0002 | g0238 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19056 | hp2 | a0002 | c0002 | t0009 | g0313 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19057 | hp2 | a0004 | c0003 | t0001 | g0065 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19062 | hp1 | a0004 | c0003 | t0001 | g0042 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19063 | hp1 | a0003 | c0004 | t0002 | g0246 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19063 | hp2 | a0005 | c0005 | t0001 | g0200 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19065 | hp1 | a0006 | c0007 | t0001 | g0341 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19065 | hp2 | a0003 | c0004 | t0002 | g0236 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19066 | hp1 | a0009 | c0012 | t0002 | g0241 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19067 | hp2 | a0004 | c0003 | t0001 | g0043 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19070 | hp1 | a0007 | c0009 | t0002 | g0235 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19075 | hp1 | a0005 | c0005 | t0001 | g0210 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19076 | hp1 | a0003 | c0004 | t0002 | g0239 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19079 | hp1 | a0004 | c0003 | t0001 | g0031 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19081 | hp1 | a0005 | c0005 | t0001 | g0205 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19081 | hp2 | a0004 | c0003 | t0001 | g0040 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19084 | hp1 | a0003 | c0004 | t0002 | g0224 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19085 | hp1 | a0006 | c0007 | t0001 | g0064 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19085 | hp2 | a0003 | c0004 | t0002 | g0230 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19088 | hp1 | a0003 | c0004 | t0002 | g0214 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19091 | hp2 | a0010 | c0014 | t0001 | g0287 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA19240 | hp2 | a0002 | c0010 | t0001 | g0268 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20129 | hp1 | a0003 | c0008 | t0004 | g0258 | AFR | ASW | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ASW | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20752 | hp2 | a0001 | c0006 | t0002 | g0092 | EUR | TSI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0334 | SAS | GIH | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG01123 | hp2 | a0011 | c0027 | t0001 | g0121 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG02559 | hp2 | a0004 | c0003 | t0001 | g0041 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03471 | hp1 | a0016 | c0020 | t0001 | g0346 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG03471 | hp2 | a0002 | c0010 | t0001 | g0271 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0325 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
HG06807 | hp2 | a0017 | c0026 | t0001 | g0164 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA18955 | hp2 | a0005 | c0005 | t0002 | g0225 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20300 | hp1 | a0004 | c0003 | t0001 | g0003 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA20300 | hp2 | a0002 | c0010 | t0001 | g0270 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA21309 | hp1 | a0003 | c0004 | t0002 | g0109 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
homoSapiens | chm13v2 | a0001 | c0013 | t0001 | g0118 | REF | REF | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0264 | REF | REF | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47335263 | C | T | 1 | a0011 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.98C>T | p.Thr33Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/25 | 535/3957 | 98/2922 | 33/973 | chr17 | 47335263 | |||
chr17:47347921 | C | T | 2 | a0005 a0011 |
28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
stop_gained | HIGH | c.631C>T | p.Arg211* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/25 | 1068/3957 | 631/2922 | 211/973 | chr17 | 47347921 | |||
chr17:47361398 | A | G | 1 | a0009 | 4 | NA18941.hp2 NA18969.hp2 NA18993.hp2 others(1): Show |
missense_variant | MODERATE | c.682A>G | p.Ile228Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/25 | 1119/3957 | 682/2922 | 228/973 | chr17 | 47361398 | |||
chr17:47361479 | C | T | 1 | a0017 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.763C>T | p.Arg255Cys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/25 | 1200/3957 | 763/2922 | 255/973 | chr17 | 47361479 | |||
chr17:47370466 | A | G | 3 | a0004 a0015 a0016 |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
missense_variant | MODERATE | c.835A>G | p.Ile279Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/25 | 1272/3957 | 835/2922 | 279/973 | chr17 | 47370466 | |||
chr17:47374528 | G | A | 11 | a0001 a0003 a0004 others(8): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
missense_variant | MODERATE | c.934G>A | p.Val312Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1371/3957 | 934/2922 | 312/973 | chr17 | 47374528 | |||
chr17:47374871 | C | G | 1 | a0001 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1277C>G | p.Ser426Cys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1714/3957 | 1277/2922 | 426/973 | chr17 | 47374871 | |||
chr17:47374891 | A | T | 1 | a0001 | 2 | HG01070.hp1 HG01071.hp1 |
stop_gained | HIGH | c.1297A>T | p.Lys433* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1734/3957 | 1297/2922 | 433/973 | chr17 | 47374891 | |||
chr17:47374952 | C | T | 1 | a0010 | 2 | NA18982.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.1358C>T | p.Ala453Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1795/3957 | 1358/2922 | 453/973 | chr17 | 47374952 | |||
chr17:47377817 | A | C | 1 | a0013 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1424A>C | p.Glu475Ala | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/25 | 1861/3957 | 1424/2922 | 475/973 | chr17 | 47377817 | |||
chr17:47391476 | A | T | 4 | a0004 a0006 a0008 others(1): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
missense_variant | MODERATE | c.1622A>T | p.Asp541Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2059/3957 | 1622/2922 | 541/973 | chr17 | 47391476 | |||
chr17:47391492 | T | G | 1 | a0001 | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
stop_gained | HIGH | c.1638T>G | p.Tyr546* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2075/3957 | 1638/2922 | 546/973 | chr17 | 47391492 | |||
chr17:47391505 | A | G | 1 | a0006 | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
missense_variant | MODERATE | c.1651A>G | p.Thr551Ala | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2088/3957 | 1651/2922 | 551/973 | chr17 | 47391505 | |||
chr17:47391532 | C | T | 1 | a0012 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1678C>T | p.Leu560Phe | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2115/3957 | 1678/2922 | 560/973 | chr17 | 47391532 | |||
chr17:47395863 | G | A | 1 | a0007 | 6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
missense_variant | MODERATE | c.1831G>A | p.Asp611Asn | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/25 | 2268/3957 | 1831/2922 | 611/973 | chr17 | 47395863 | |||
chr17:47409691 | G | A | 1 | a0014 | 1 | HG03017.hp1 | missense_variant&splice_region_variant | MODERATE | c.2278G>A | p.Glu760Lys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/25 | 2715/3957 | 2278/2922 | 760/973 | chr17 | 47409691 | |||
chr17:47414888 | G | T | 1 | a0015 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.2463G>T | p.Met821Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/25 | 2900/3957 | 2463/2922 | 821/973 | chr17 | 47414888 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47344197 | G | A | 2 | a0006c0007 a0008c0011 |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
synonymous_variant | LOW | c.339G>A | p.Lys113Lys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/25 | 776/3957 | 339/2922 | 113/973 | chr17 | 47344197 | |||
chr17:47374567 | T | C | 1 | a0003c0016 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.973T>C | p.Leu325Leu | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1410/3957 | 973/2922 | 325/973 | chr17 | 47374567 | |||
chr17:47374878 | C | A | 1 | a0001c0022 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1284C>A | p.Ile428Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1721/3957 | 1284/2922 | 428/973 | chr17 | 47374878 | |||
chr17:47374935 | G | A | 1 | a0001c0023 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1341G>A | p.Ser447Ser | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1778/3957 | 1341/2922 | 447/973 | chr17 | 47374935 | |||
chr17:47394077 | G | A | 1 | a0002c0010 | 6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.1779G>A | p.Thr593Thr | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/25 | 2216/3957 | 1779/2922 | 593/973 | chr17 | 47394077 | |||
chr17:47412885 | C | T | 10 | a0003c0004 a0003c0016 a0004c0003 others(7): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
synonymous_variant | LOW | c.2391C>T | p.Phe797Phe | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/25 | 2828/3957 | 2391/2922 | 797/973 | chr17 | 47412885 | |||
chr17:47412909 | C | T | 2 | a0001c0015 a0001c0024 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
synonymous_variant | LOW | c.2415C>T | p.Asn805Asn | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/25 | 2852/3957 | 2415/2922 | 805/973 | chr17 | 47412909 | |||
chr17:47440579 | G | A | 1 | a0001c0024 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.2787G>A | p.Gln929Gln | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 3224/3957 | 2787/2922 | 929/973 | chr17 | 47440579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47323969 | T | C | 8 | a0001c0001t0002 a0001c0006t0002 a0001c0023t0002 others(5): Show |
47 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-423T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/25 | 4385 | chr17 | 47323969 | ||||||
chr17:47324048 | G | A | 1 | a0001c0001t0005 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-344G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/25 | 4306 | chr17 | 47324048 | ||||||
chr17:47326340 | C | T | 2 | a0004c0003t0006 a0015c0021t0006 |
2 | HG03130.hp1 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/25 | chr17 | 47326340 | |||||||
chr17:47326350 | C | A | 1 | a0005c0005t0007 | 1 | HG03704.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/25 | chr17 | 47326350 | |||||||
chr17:47328318 | A | C | 1 | a0006c0007t0010 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/25 | 36 | chr17 | 47328318 | ||||||
chr17:47440827 | A | G | 1 | a0003c0008t0004 | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*113A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 113 | chr17 | 47440827 | ||||||
chr17:47440839 | A | G | 1 | a0002c0002t0009 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 125 | chr17 | 47440839 | ||||||
chr17:47440846 | G | A | 1 | a0002c0002t0008 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 132 | chr17 | 47440846 | ||||||
chr17:47441217 | T | G | 4 | a0001c0006t0003 a0002c0002t0003 a0003c0008t0003 others(1): Show |
17 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*503T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 503 | chr17 | 47441217 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47324135 | G | T | 5 | a0002c0002t0001g0347 a0002c0002t0001g0348 a0002c0002t0001g0349 others(2): Show |
5 | HG02922.hp2 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-318+61G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324135 | |||||||
chr17:47324314 | T | G | 2 | a0003c0008t0001g0006 a0003c0008t0004g0005 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-317-140T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324314 | |||||||
chr17:47324345 | T | G | 261 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-317-109T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324345 | |||||||
chr17:47324351 | T | C | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-317-103T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324351 | |||||||
chr17:47324391 | A | G | 261 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-317-63A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324391 | |||||||
chr17:47324415 | G | T | 1 | a0003c0008t0004g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-317-39G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324415 | |||||||
chr17:47324426 | A | G | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-317-28A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324426 | |||||||
chr17:47324435 | G | C | 2 | a0005c0005t0001g0007 a0005c0005t0001g0008 |
2 | HG00438.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-317-19G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324435 | |||||||
chr17:47324630 | T | C | 4 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0003c0008t0004g0011 others(1): Show |
4 | HG01106.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-248+107T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324630 | |||||||
chr17:47324644 | G | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+121G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324644 | |||||||
chr17:47324842 | C | T | 203 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(200): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-248+319C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324842 | |||||||
chr17:47324913 | C | G | 296 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(293): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-248+390C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324913 | |||||||
chr17:47324919 | T | TGTCTCCT others(19): Show |
1 | a0001c0001t0001g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-248+397_-248+422d others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47324919 | ||||||
chr17:47324974 | T | A | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-248+451T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324974 | |||||||
chr17:47325025 | C | CCCCCCCC others(257): Show |
1 | a0005c0005t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(266): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | ||||||
chr17:47325025 | C | CCCCCCCC others(264): Show |
1 | a0001c0025t0001g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | ||||||
chr17:47325025 | C | CCCCCCCC others(249): Show |
1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | ||||||
chr17:47325026 | C | CCCACCCC others(275): Show |
1 | a0005c0005t0001g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-248+505_-248+506i others(284): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCACCCC others(276): Show |
1 | a0005c0005t0001g0342 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-248+505_-248+506i others(285): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(277): Show |
1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(286): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(278): Show |
1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(287): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(245): Show |
2 | a0001c0006t0002g0072 a0001c0006t0002g0073 |
2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(254): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(250): Show |
1 | a0005c0005t0001g0074 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(259): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(251): Show |
1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(260): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(263): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG00323.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(272): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(264): Show |
3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG01361.hp1 NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(265): Show |
8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG00741.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(274): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(268): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(277): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(270): Show |
1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(279): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(273): Show |
1 | a0001c0001t0001g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(282): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(274): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(283): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(279): Show |
1 | a0001c0001t0001g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(288): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(244): Show |
9 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(253): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(245): Show |
2 | a0001c0006t0002g0102 a0001c0006t0003g0101 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(254): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(246): Show |
3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(255): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(248): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01169.hp2 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(257): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(249): Show |
2 | a0001c0001t0001g0108 a0003c0004t0002g0109 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(250): Show |
1 | a0005c0005t0001g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(259): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(251): Show |
1 | a0001c0001t0001g0111 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(260): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(252): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG01175.hp2 NA18944.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(261): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(253): Show |
1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(262): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(253): Show |
1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(262): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(258): Show |
1 | a0005c0005t0001g0116 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(267): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(259): Show |
1 | a0005c0005t0003g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(268): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(260): Show |
1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(269): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(262): Show |
3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0011c0027t0001g0121 |
3 | HG01123.hp2 HG01168.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(271): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(263): Show |
22 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(19): Show |
22 | HG01074.hp2 HG01123.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(272): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(264): Show |
20 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(17): Show |
20 | HG00642.hp2 HG01069.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(265): Show |
7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG01070.hp2 HG02257.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(274): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(266): Show |
8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(275): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(267): Show |
7 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG00673.hp2 HG01496.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(276): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(268): Show |
3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0275 |
3 | HG02647.hp1 HG02735.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(277): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(269): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG00280.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(278): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(270): Show |
10 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(7): Show |
10 | HG01192.hp1 HG01884.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(279): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(271): Show |
1 | a0001c0013t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(280): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(272): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0198 a0001c0013t0001g0197 |
3 | HG01071.hp1 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(281): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(273): Show |
7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0005c0005t0001g0007 others(4): Show |
7 | HG01517.hp1 HG02683.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(282): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(274): Show |
8 | a0005c0005t0001g0008 a0005c0005t0001g0205 a0005c0005t0001g0206 others(5): Show |
8 | HG00438.hp1 HG00544.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(283): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(275): Show |
1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(284): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(276): Show |
1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(285): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(280): Show |
1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(289): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCC others(282): Show |
1 | a0001c0001t0001g0345 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(291): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCT others(247): Show |
1 | a0003c0004t0002g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(256): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCT others(248): Show |
25 | a0001c0001t0002g0217 a0001c0023t0002g0229 a0003c0004t0002g0216 others(22): Show |
26 | HG00544.hp1 HG00558.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(257): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCT others(249): Show |
15 | a0001c0001t0002g0242 a0003c0004t0002g0240 a0003c0004t0002g0243 others(12): Show |
15 | HG00438.hp2 HG01515.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325026 | C | CCCCCCCT others(262): Show |
1 | a0001c0001t0001g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(271): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | ||||||
chr17:47325031 | T | C | 210 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(207): Show |
211 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-248+508T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325031 | |||||||
chr17:47325161 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-248+638A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325161 | |||||||
chr17:47325222 | C | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-248+699C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325222 | |||||||
chr17:47325224 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-248+701A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325224 | |||||||
chr17:47325511 | C | T | 2 | a0005c0005t0001g0210 a0005c0005t0001g0211 |
2 | HG00544.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-247-715C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325511 | |||||||
chr17:47325534 | A | G | 17 | a0001c0001t0001g0107 a0003c0008t0004g0011 a0003c0008t0004g0012 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.-247-692A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325534 | |||||||
chr17:47325691 | T | C | 265 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-247-535T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325691 | |||||||
chr17:47325803 | CT | C | 5 | a0004c0003t0001g0003 a0004c0003t0001g0020 a0004c0003t0001g0021 others(2): Show |
6 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-247-413delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325803 | ||||||
chr17:47325846 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-247-380A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325846 | |||||||
chr17:47325862 | A | AT | 67 | a0002c0002t0001g0002 a0002c0002t0001g0056 a0002c0002t0001g0259 others(64): Show |
69 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.-247-361dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325862 | ||||||
chr17:47325920 | CAA | C | 3 | a0002c0010t0001g0267 a0002c0010t0001g0268 a0002c0010t0001g0269 |
3 | HG02615.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-247-303_-247-302d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325920 | ||||||
chr17:47325921 | AAAATATA others(25): Show |
A | 37 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-247-303_-247-272d others(34): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325921 | ||||||
chr17:47325923 | A | AAT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0169 others(13): Show |
16 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-247-265_-247-264d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATAT | 13 | a0001c0001t0001g0014 a0001c0001t0001g0113 a0002c0002t0001g0278 others(10): Show |
13 | HG01074.hp1 HG01175.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-247-267_-247-264d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATAT | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 others(24): Show |
27 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.-247-269_-247-264d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(1): Show |
27 | a0001c0001t0001g0019 a0001c0001t0001g0105 a0001c0001t0001g0108 others(24): Show |
27 | HG00544.hp2 HG01243.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.-247-271_-247-264d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(3): Show |
24 | a0001c0001t0001g0051 a0001c0001t0001g0173 a0001c0001t0001g0180 others(21): Show |
24 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-247-273_-247-264d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(5): Show |
10 | a0001c0001t0001g0203 a0002c0002t0003g0338 a0003c0004t0002g0230 others(7): Show |
10 | HG01069.hp1 HG02056.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-275_-247-264d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(7): Show |
10 | a0001c0001t0001g0174 a0001c0001t0001g0345 a0003c0004t0002g0109 others(7): Show |
10 | HG01123.hp2 HG02738.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-277_-247-264d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(9): Show |
3 | a0003c0004t0002g0237 a0003c0004t0002g0238 a0005c0005t0001g0204 |
3 | HG03834.hp1 NA18990.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-247-279_-247-264d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-247-281_-247-264d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | A | T | 2 | a0002c0010t0001g0270 a0002c0010t0001g0271 |
2 | HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-247-303A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325923 | |||||||
chr17:47325923 | AAT | A | 27 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0070 others(24): Show |
27 | HG01192.hp2 HG01255.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-247-265_-247-264d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATAT | A | 10 | a0002c0002t0001g0009 a0002c0002t0001g0272 a0002c0002t0001g0281 others(7): Show |
11 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-247-267_-247-264d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(1): Show |
A | 5 | a0001c0001t0001g0187 a0002c0002t0001g0262 a0003c0008t0004g0157 others(2): Show |
5 | HG00408.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-247-271_-247-264d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(3): Show |
A | 9 | a0001c0006t0001g0100 a0001c0006t0002g0102 a0006c0007t0001g0059 others(6): Show |
9 | HG00423.hp2 HG01081.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-247-273_-247-264d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(5): Show |
A | 10 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(7): Show |
10 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-275_-247-264d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(7): Show |
A | 2 | a0001c0006t0002g0072 a0001c0006t0002g0092 |
2 | HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-247-277_-247-264d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(9): Show |
A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0184 others(5): Show |
8 | HG01256.hp2 HG01517.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-247-279_-247-264d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(11): Show |
A | 49 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(46): Show |
49 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-247-281_-247-264d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(13): Show |
A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-247-283_-247-264d others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(15): Show |
A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-247-285_-247-264d others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325923 | AATATATA others(17): Show |
A | 6 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(3): Show |
6 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-247-287_-247-264d others(26): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | ||||||
chr17:47325937 | T | TATATATA others(24): Show |
1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-247-264_-247-263i others(33): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325937 | ||||||
chr17:47325941 | T | TAAACAAA | 16 | a0001c0001t0001g0088 a0001c0001t0001g0111 a0001c0001t0001g0135 others(13): Show |
16 | NA18943.hp1 NA18946.hp2 NA18962.hp2 others(13): Show |
intron_variant | MODIFIER | c.-247-284_-247-283i others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325941 | ||||||
chr17:47325943 | TATATATA others(14): Show |
T | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-247-272_-247-252d others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325943 | ||||||
chr17:47325960 | A | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-247-266A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325960 | |||||||
chr17:47325963 | G | A | 3 | a0005c0005t0001g0007 a0005c0005t0001g0008 a0005c0005t0001g0200 |
3 | HG00438.hp1 NA18985.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-247-263G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325963 | |||||||
chr17:47325963 | G | T | 23 | a0002c0002t0001g0089 a0005c0005t0001g0069 a0005c0005t0001g0074 others(20): Show |
23 | HG00408.hp2 HG00544.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.-247-263G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325963 | |||||||
chr17:47325964 | C | T | 3 | a0005c0005t0001g0007 a0005c0005t0001g0008 a0005c0005t0001g0200 |
3 | HG00438.hp1 NA18985.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-247-262C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325964 | |||||||
chr17:47326079 | A | T | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-247-147A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47326079 | |||||||
chr17:47326105 | C | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-247-121C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47326105 | |||||||
chr17:47326404 | G | A | 56 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(53): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-86+17G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326404 | |||||||
chr17:47326607 | A | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-86+220A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326607 | |||||||
chr17:47326683 | C | CAGT | 35 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-86+300_-86+302dup others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr17 | 47326683 | ||||||
chr17:47326744 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-86+357G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326744 | |||||||
chr17:47327026 | C | T | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+639C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327026 | |||||||
chr17:47327060 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-86+673A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327060 | |||||||
chr17:47327119 | G | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-86+732G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327119 | |||||||
chr17:47327156 | A | C | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-86+769A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327156 | |||||||
chr17:47327166 | GTTTTC | G | 56 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(53): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-86+784_-86+788del others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr17 | 47327166 | ||||||
chr17:47327171 | C | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-86+784C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327171 | |||||||
chr17:47327325 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+938C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327325 | |||||||
chr17:47327358 | T | A | 3 | a0004c0003t0006g0260 a0015c0021t0006g0261 a0016c0020t0001g0346 |
3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-85-911T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327358 | |||||||
chr17:47327398 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-85-871C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327398 | |||||||
chr17:47327479 | A | C | 1 | a0002c0002t0003g0338 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-85-790A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327479 | |||||||
chr17:47327495 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-774T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327495 | |||||||
chr17:47327543 | C | T | 2 | a0002c0002t0001g0334 a0014c0018t0001g0337 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-726C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327543 | |||||||
chr17:47327550 | C | T | 19 | a0002c0002t0001g0056 a0002c0002t0001g0272 a0002c0002t0001g0285 others(16): Show |
19 | HG00673.hp1 HG01106.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-85-719C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327550 | |||||||
chr17:47327571 | C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-85-698C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327571 | |||||||
chr17:47327645 | C | T | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-85-624C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327645 | |||||||
chr17:47327691 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-85-578A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327691 | |||||||
chr17:47327697 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-85-572C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327697 | |||||||
chr17:47327778 | G | A | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-85-491G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327778 | |||||||
chr17:47327919 | T | C | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-85-350T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327919 | |||||||
chr17:47327935 | C | T | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-85-334C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327935 | |||||||
chr17:47328082 | G | A | 1 | a0002c0002t0003g0331 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-85-187G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47328082 | |||||||
chr17:47328191 | A | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-85-78A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47328191 | |||||||
chr17:47328509 | A | G | 1 | a0004c0003t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.30+126A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328509 | |||||||
chr17:47328543 | T | A | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.30+160T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328543 | |||||||
chr17:47328622 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+239T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328622 | |||||||
chr17:47328793 | A | G | 1 | a0004c0003t0001g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.30+410A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328793 | |||||||
chr17:47328801 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.30+418A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328801 | |||||||
chr17:47328864 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.30+481T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328864 | |||||||
chr17:47328933 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.30+550G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328933 | |||||||
chr17:47328979 | T | C | 266 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(263): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.30+596T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328979 | |||||||
chr17:47329084 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+701T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329084 | |||||||
chr17:47329241 | G | C | 1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.30+858G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329241 | |||||||
chr17:47329362 | A | G | 42 | a0003c0008t0001g0006 a0003c0008t0001g0134 a0003c0008t0004g0005 others(39): Show |
45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+979A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329362 | |||||||
chr17:47329489 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+1106T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329489 | |||||||
chr17:47329689 | G | C | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1306G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329689 | |||||||
chr17:47329705 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+1322T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329705 | |||||||
chr17:47329985 | C | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1602C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329985 | |||||||
chr17:47330147 | A | T | 42 | a0003c0008t0001g0006 a0003c0008t0001g0134 a0003c0008t0004g0005 others(39): Show |
45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+1764A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330147 | |||||||
chr17:47330242 | C | A | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+1859C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330242 | |||||||
chr17:47330251 | T | A | 58 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(55): Show |
59 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.30+1868T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330251 | |||||||
chr17:47330279 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+1896T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330279 | |||||||
chr17:47330287 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+1904G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330287 | |||||||
chr17:47330290 | G | A | 1 | a0001c0015t0001g0106 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.30+1907G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330290 | |||||||
chr17:47330489 | C | A | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+2106C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330489 | |||||||
chr17:47330649 | G | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.30+2266G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330649 | |||||||
chr17:47330788 | C | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+2405C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330788 | |||||||
chr17:47330802 | C | T | 1 | a0005c0005t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.30+2419C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330802 | |||||||
chr17:47331019 | T | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+2636T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331019 | |||||||
chr17:47331102 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.30+2719A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331102 | |||||||
chr17:47331489 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3106C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331489 | |||||||
chr17:47331508 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+3125G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331508 | |||||||
chr17:47331803 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31-3393T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331803 | |||||||
chr17:47331905 | A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-3291A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331905 | |||||||
chr17:47331947 | G | A | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.31-3249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331947 | |||||||
chr17:47332020 | T | A | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.31-3176T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332020 | |||||||
chr17:47332077 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0173 a0001c0001t0001g0182 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3119A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332077 | |||||||
chr17:47332639 | A | T | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-2557A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332639 | |||||||
chr17:47332768 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-2428G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332768 | |||||||
chr17:47332778 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.31-2418G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332778 | |||||||
chr17:47332793 | AT | A | 3 | a0004c0003t0006g0260 a0015c0021t0006g0261 a0016c0020t0001g0346 |
3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-2399delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr17 | 47332793 | ||||||
chr17:47332823 | C | T | 1 | a0002c0002t0001g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.31-2373C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332823 | |||||||
chr17:47333020 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.31-2176C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333020 | |||||||
chr17:47333100 | G | A | 98 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(95): Show |
102 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.31-2096G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333100 | |||||||
chr17:47333213 | A | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-1983A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333213 | |||||||
chr17:47333324 | G | T | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.31-1872G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333324 | |||||||
chr17:47333398 | A | C | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.31-1798A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333398 | |||||||
chr17:47333653 | A | T | 3 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 |
3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31-1543A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333653 | |||||||
chr17:47333718 | C | T | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31-1478C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333718 | |||||||
chr17:47333977 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-1219A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333977 | |||||||
chr17:47333993 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0193 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.31-1203G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333993 | |||||||
chr17:47334029 | T | C | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-1167T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334029 | |||||||
chr17:47334047 | T | C | 3 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG03654.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-1149T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334047 | |||||||
chr17:47334121 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-1075T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334121 | |||||||
chr17:47334126 | G | GT | 105 | a0001c0001t0001g0104 a0001c0006t0001g0093 a0001c0006t0001g0094 others(102): Show |
109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.31-1060dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr17 | 47334126 | ||||||
chr17:47334477 | A | G | 38 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(35): Show |
41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-719A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334477 | |||||||
chr17:47334653 | T | C | 51 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(48): Show |
54 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.31-543T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334653 | |||||||
chr17:47334788 | G | C | 3 | a0004c0003t0006g0260 a0015c0021t0006g0261 a0016c0020t0001g0346 |
3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-408G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334788 | |||||||
chr17:47334876 | C | T | 1 | a0004c0003t0001g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.31-320C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334876 | |||||||
chr17:47334965 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31-231A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334965 | |||||||
chr17:47334981 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-215G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334981 | |||||||
chr17:47335676 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0025t0001g0144 |
3 | HG01099.hp1 NA18948.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.191+320C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47335676 | |||||||
chr17:47335975 | T | C | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+619T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47335975 | |||||||
chr17:47336018 | G | A | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.191+662G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336018 | |||||||
chr17:47336087 | G | C | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.191+731G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336087 | |||||||
chr17:47336129 | GT | G | 92 | a0001c0001t0001g0135 a0002c0002t0001g0303 a0003c0004t0001g0141 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.191+788delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336129 | ||||||
chr17:47336240 | C | T | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+884C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336240 | |||||||
chr17:47336292 | A | AT | 6 | a0004c0003t0001g0022 a0004c0003t0001g0046 a0008c0011t0001g0049 others(3): Show |
6 | HG01109.hp1 HG02056.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+953dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | ||||||
chr17:47336292 | AT | A | 153 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(150): Show |
153 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.191+953delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | ||||||
chr17:47336292 | ATTT | A | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.191+951_191+953del others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | ||||||
chr17:47336581 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.191+1225G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336581 | |||||||
chr17:47336592 | AT | A | 31 | a0001c0001t0001g0103 a0001c0001t0001g0113 a0001c0001t0001g0140 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+1256delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | ||||||
chr17:47336592 | ATT | A | 196 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(193): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.191+1255_191+1256d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | ||||||
chr17:47336592 | ATTT | A | 43 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(40): Show |
44 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.191+1254_191+1256d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | ||||||
chr17:47337256 | C | G | 1 | a0002c0002t0003g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.191+1900C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337256 | |||||||
chr17:47337299 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+1943T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337299 | |||||||
chr17:47337304 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.191+1948G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337304 | |||||||
chr17:47337460 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.191+2104T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337460 | |||||||
chr17:47337609 | A | G | 5 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 others(2): Show |
5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+2253A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337609 | |||||||
chr17:47337641 | T | C | 37 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.191+2285T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337641 | |||||||
chr17:47337775 | G | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.191+2419G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337775 | |||||||
chr17:47337886 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191+2530T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337886 | |||||||
chr17:47338243 | GT | G | 206 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(203): Show |
210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.191+2904delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338243 | ||||||
chr17:47338411 | G | A | 38 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(35): Show |
41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+3055G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338411 | |||||||
chr17:47338558 | G | GTT | 89 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(86): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.191+3212_191+3213d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338558 | ||||||
chr17:47338570 | A | T | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.191+3214A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338570 | |||||||
chr17:47338631 | C | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.191+3275C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338631 | |||||||
chr17:47338895 | T | TA | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.192-3020dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338895 | ||||||
chr17:47339172 | T | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-2749T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339172 | |||||||
chr17:47339436 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.192-2485G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339436 | |||||||
chr17:47339517 | C | T | 1 | a0005c0005t0001g0207 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.192-2404C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339517 | |||||||
chr17:47339631 | A | G | 334 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.192-2290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339631 | |||||||
chr17:47339699 | C | CA | 63 | a0001c0001t0001g0123 a0002c0002t0001g0002 a0002c0002t0001g0056 others(60): Show |
65 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.192-2206dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | ||||||
chr17:47339699 | C | CAAA | 6 | a0004c0003t0001g0023 a0004c0003t0001g0025 a0008c0011t0001g0049 others(3): Show |
6 | HG01975.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-2208_192-2206d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | ||||||
chr17:47339699 | C | CAAAA | 44 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(41): Show |
47 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.192-2209_192-2206d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | ||||||
chr17:47339848 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-2073A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339848 | |||||||
chr17:47339959 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.192-1962A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339959 | |||||||
chr17:47340189 | A | G | 2 | a0004c0003t0006g0260 a0015c0021t0006g0261 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.192-1732A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340189 | |||||||
chr17:47340276 | A | G | 1 | a0004c0003t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.192-1645A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340276 | |||||||
chr17:47340366 | T | G | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.192-1555T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340366 | |||||||
chr17:47340448 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-1473C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340448 | |||||||
chr17:47340552 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.192-1369T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340552 | |||||||
chr17:47340564 | A | G | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.192-1357A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340564 | |||||||
chr17:47340745 | G | A | 138 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.192-1176G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340745 | |||||||
chr17:47340766 | A | AT | 10 | a0002c0002t0001g0010 a0002c0002t0001g0294 a0002c0002t0001g0308 others(7): Show |
10 | HG00423.hp1 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-1126dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340766 | AT | A | 126 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.192-1126delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340766 | ATT | A | 22 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0124 others(19): Show |
22 | HG00323.hp1 HG01069.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.192-1127_192-1126d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340766 | ATTT | A | 43 | a0003c0004t0002g0239 a0003c0008t0001g0134 a0004c0003t0001g0001 others(40): Show |
46 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.192-1128_192-1126d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340766 | ATTTT | A | 42 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(39): Show |
43 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.192-1129_192-1126d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340766 | ATTTTTTT others(5): Show |
A | 1 | a0005c0005t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.192-1137_192-1126d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | ||||||
chr17:47340804 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-1117C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340804 | |||||||
chr17:47341088 | G | A | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.192-833G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341088 | |||||||
chr17:47341464 | T | TC | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.192-457_192-456ins others(1): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341464 | |||||||
chr17:47341576 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.192-345G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341576 | |||||||
chr17:47341670 | C | CA | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-244dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47341670 | ||||||
chr17:47341695 | T | G | 96 | a0002c0002t0001g0002 a0002c0002t0001g0056 a0002c0002t0001g0089 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.192-226T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341695 | |||||||
chr17:47341743 | A | G | 42 | a0003c0008t0001g0006 a0003c0008t0001g0134 a0003c0008t0004g0005 others(39): Show |
45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.192-178A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341743 | |||||||
chr17:47341773 | A | G | 29 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0091 others(26): Show |
29 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.192-148A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341773 | |||||||
chr17:47342082 | G | A | 1 | a0005c0005t0003g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.303+50G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342082 | |||||||
chr17:47342101 | A | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.303+69A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342101 | |||||||
chr17:47342260 | A | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.303+228A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342260 | |||||||
chr17:47342480 | A | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+448A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342480 | |||||||
chr17:47342558 | C | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.303+526C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342558 | |||||||
chr17:47343064 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.303+1032G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343064 | |||||||
chr17:47343133 | A | G | 1 | a0002c0002t0008g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.304-1029A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343133 | |||||||
chr17:47343167 | C | G | 1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.304-995C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343167 | |||||||
chr17:47343579 | G | C | 2 | a0005c0005t0001g0007 a0005c0005t0001g0008 |
2 | HG00438.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.304-583G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343579 | |||||||
chr17:47343590 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304-572C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343590 | |||||||
chr17:47343626 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-536C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343626 | |||||||
chr17:47343636 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.304-526A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343636 | |||||||
chr17:47343666 | T | A | 2 | a0006c0007t0001g0059 a0006c0007t0001g0062 |
2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.304-496T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343666 | |||||||
chr17:47343763 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-399C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343763 | |||||||
chr17:47343869 | A | G | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.304-293A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343869 | |||||||
chr17:47343907 | G | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.304-255G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343907 | |||||||
chr17:47344824 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.435-192T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/24 | chr17 | 47344824 | |||||||
chr17:47344919 | C | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.435-97C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/24 | chr17 | 47344919 | |||||||
chr17:47345239 | G | A | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.517+141G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345239 | |||||||
chr17:47345262 | A | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.517+164A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345262 | |||||||
chr17:47345319 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.517+221G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345319 | |||||||
chr17:47345367 | T | G | 52 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(49): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.517+269T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345367 | |||||||
chr17:47345567 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.517+469G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345567 | |||||||
chr17:47345650 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+552C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345650 | |||||||
chr17:47345694 | C | T | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.517+596C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345694 | |||||||
chr17:47345912 | A | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.517+814A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345912 | |||||||
chr17:47346004 | G | T | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.517+906G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346004 | |||||||
chr17:47346018 | T | C | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.517+920T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346018 | |||||||
chr17:47346105 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.517+1007G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346105 | |||||||
chr17:47346131 | T | C | 1 | a0008c0011t0001g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517+1033T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346131 | |||||||
chr17:47346203 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517+1105A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346203 | |||||||
chr17:47346256 | A | T | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1158A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346256 | |||||||
chr17:47346353 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517+1255A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346353 | |||||||
chr17:47346433 | A | AC | 93 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(90): Show |
95 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.517+1346dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | ||||||
chr17:47346433 | A | ACC | 90 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.517+1345_517+1346d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | ||||||
chr17:47346433 | A | ACCC | 36 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0080 others(33): Show |
36 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+1344_517+1346d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | ||||||
chr17:47346433 | AC | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.517+1346delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | ||||||
chr17:47346435 | C | CCG | 18 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
18 | HG02135.hp1 HG02257.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.517+1338_517+1339i others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346435 | ||||||
chr17:47346440 | C | CG | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.517+1342_517+1343i others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346440 | |||||||
chr17:47346526 | A | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.518-1282A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346526 | |||||||
chr17:47346661 | C | G | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.518-1147C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346661 | |||||||
chr17:47346661 | C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-1147C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346661 | |||||||
chr17:47346871 | A | C | 5 | a0003c0004t0002g0224 a0003c0004t0002g0232 a0003c0004t0002g0236 others(2): Show |
5 | NA18612.hp1 NA18964.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-937A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346871 | |||||||
chr17:47347017 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-791G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347017 | |||||||
chr17:47347033 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.518-775A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347033 | |||||||
chr17:47347048 | T | C | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-760T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347048 | |||||||
chr17:47347178 | G | A | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-630G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347178 | |||||||
chr17:47347180 | T | G | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518-628T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347180 | |||||||
chr17:47347191 | C | T | 44 | a0002c0002t0001g0307 a0002c0002t0001g0314 a0002c0002t0009g0313 others(41): Show |
45 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.518-617C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347191 | |||||||
chr17:47347200 | G | A | 3 | a0007c0009t0001g0221 a0007c0009t0002g0248 a0007c0009t0002g0252 |
3 | NA18961.hp2 NA18975.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.518-608G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347200 | |||||||
chr17:47347296 | T | C | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-512T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347296 | |||||||
chr17:47347417 | GA | G | 57 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-385delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47347417 | ||||||
chr17:47347423 | A | C | 1 | a0002c0002t0001g0306 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.518-385A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347423 | |||||||
chr17:47347508 | A | C | 19 | a0003c0004t0002g0214 a0003c0004t0002g0216 a0003c0004t0002g0219 others(16): Show |
20 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-300A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347508 | |||||||
chr17:47347531 | G | A | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518-277G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347531 | |||||||
chr17:47347650 | A | G | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-158A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347650 | |||||||
chr17:47347749 | G | A | 120 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
120 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(117): Show |
intron_variant | MODIFIER | c.518-59G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347749 | |||||||
chr17:47347778 | C | T | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.518-30C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347778 | |||||||
chr17:47347788 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.518-20G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347788 | |||||||
chr17:47348162 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+211G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348162 | |||||||
chr17:47348183 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.661+232G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348183 | |||||||
chr17:47348190 | G | A | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+239G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348190 | |||||||
chr17:47348213 | C | T | 17 | a0001c0001t0001g0052 a0001c0006t0001g0093 a0001c0006t0001g0094 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+262C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348213 | |||||||
chr17:47348238 | C | T | 138 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.661+287C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348238 | |||||||
chr17:47348331 | T | G | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.661+380T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348331 | |||||||
chr17:47348390 | T | A | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+439T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348390 | |||||||
chr17:47348414 | T | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.661+463T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348414 | |||||||
chr17:47348555 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.661+604A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348555 | |||||||
chr17:47348755 | T | TGAAAAAT others(321): Show |
1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+815_661+816ins others(328): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47348755 | ||||||
chr17:47348755 | T | TGAAAAAT others(325): Show |
1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.661+815_661+816ins others(332): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47348755 | ||||||
chr17:47348774 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.661+823T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348774 | |||||||
chr17:47348904 | A | G | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661+953A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348904 | |||||||
chr17:47349554 | G | A | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.661+1603G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349554 | |||||||
chr17:47349759 | C | CT | 7 | a0002c0002t0001g0314 a0002c0002t0001g0332 a0002c0002t0001g0333 others(4): Show |
7 | HG00438.hp1 HG02572.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+1834dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | ||||||
chr17:47349759 | CT | C | 55 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0070 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.661+1834delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | ||||||
chr17:47349759 | CTT | C | 89 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
89 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.661+1833_661+1834d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | ||||||
chr17:47349759 | CTTTTTT | C | 49 | a0003c0004t0001g0141 a0004c0003t0001g0001 a0004c0003t0001g0003 others(46): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.661+1829_661+1834d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | ||||||
chr17:47349759 | CTTTTTTT | C | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.661+1828_661+1834d others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | ||||||
chr17:47349768 | T | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+1817T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349768 | |||||||
chr17:47349812 | G | T | 1 | a0006c0007t0001g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.661+1861G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349812 | |||||||
chr17:47349815 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.661+1864T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349815 | |||||||
chr17:47349822 | C | T | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661+1871C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349822 | |||||||
chr17:47349932 | G | A | 25 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(22): Show |
28 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.661+1981G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349932 | |||||||
chr17:47349935 | T | C | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.661+1984T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349935 | |||||||
chr17:47349996 | G | A | 1 | a0003c0004t0002g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.661+2045G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349996 | |||||||
chr17:47350054 | G | A | 95 | a0002c0002t0001g0002 a0002c0002t0001g0056 a0002c0002t0001g0089 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.661+2103G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350054 | |||||||
chr17:47350063 | C | T | 2 | a0006c0007t0001g0059 a0006c0007t0001g0062 |
2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.661+2112C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350063 | |||||||
chr17:47350142 | C | A | 28 | a0005c0005t0001g0007 a0005c0005t0001g0008 a0005c0005t0001g0068 others(25): Show |
28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.661+2191C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350142 | |||||||
chr17:47350533 | T | G | 29 | a0002c0002t0003g0328 a0005c0005t0001g0007 a0005c0005t0001g0008 others(26): Show |
29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+2582T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350533 | |||||||
chr17:47350585 | T | G | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+2634T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350585 | |||||||
chr17:47350601 | G | GT | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.661+2659dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47350601 | ||||||
chr17:47350603 | T | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+2652T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350603 | |||||||
chr17:47350783 | G | A | 17 | a0001c0001t0001g0088 a0001c0001t0001g0111 a0001c0001t0001g0135 others(14): Show |
17 | NA18943.hp1 NA18946.hp2 NA18962.hp2 others(14): Show |
intron_variant | MODIFIER | c.661+2832G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350783 | |||||||
chr17:47350847 | G | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.661+2896G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350847 | |||||||
chr17:47350873 | G | A | 1 | a0004c0003t0001g0046 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.661+2922G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350873 | |||||||
chr17:47351051 | C | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+3100C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351051 | |||||||
chr17:47351118 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.661+3167C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351118 | |||||||
chr17:47351140 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+3189A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351140 | |||||||
chr17:47351279 | C | CTG | 28 | a0001c0022t0001g0194 a0002c0002t0001g0266 a0002c0002t0003g0336 others(25): Show |
29 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+3353_661+3354d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTG | 28 | a0001c0001t0001g0091 a0001c0001t0001g0113 a0001c0001t0001g0138 others(25): Show |
28 | HG00673.hp2 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.661+3351_661+3354d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTG | 49 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0080 others(46): Show |
52 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.661+3349_661+3354d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(1): Show |
42 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0086 others(39): Show |
42 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.661+3347_661+3354d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(3): Show |
36 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(33): Show |
36 | HG01243.hp1 HG01433.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+3345_661+3354d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(5): Show |
26 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0052 others(23): Show |
26 | HG00280.hp2 HG01081.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.661+3343_661+3354d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(7): Show |
10 | a0001c0001t0001g0013 a0001c0001t0001g0132 a0001c0001t0001g0142 others(7): Show |
10 | HG02109.hp1 HG02135.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.661+3341_661+3354d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(9): Show |
2 | a0006c0007t0001g0339 a0006c0007t0001g0340 |
2 | HG00423.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.661+3339_661+3354d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(11): Show |
5 | a0001c0001t0001g0143 a0002c0002t0003g0055 a0006c0007t0001g0063 others(2): Show |
5 | HG01361.hp2 HG02647.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3337_661+3354d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | C | CTGTGTGT others(13): Show |
1 | a0002c0002t0003g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.661+3335_661+3354d others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | CTGTG | C | 7 | a0002c0002t0001g0089 a0002c0002t0001g0283 a0002c0002t0001g0307 others(4): Show |
7 | HG02486.hp2 NA18612.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+3351_661+3354d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351279 | CTGTGTG | C | 21 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0285 others(18): Show |
21 | HG01358.hp2 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.661+3349_661+3354d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | ||||||
chr17:47351296 | T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3345T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351296 | |||||||
chr17:47351296 | TGTGTGTG others(11): Show |
T | 29 | a0002c0002t0003g0328 a0005c0005t0001g0007 a0005c0005t0001g0008 others(26): Show |
29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+3347_661+3364d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351296 | ||||||
chr17:47351298 | T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3347T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351298 | |||||||
chr17:47351298 | TGTGTGTG others(9): Show |
T | 5 | a0002c0002t0001g0002 a0002c0002t0001g0303 a0002c0002t0001g0304 others(2): Show |
7 | HG02083.hp2 NA18945.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+3349_661+3364d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | ||||||
chr17:47351298 | TGTGTGTG others(11): Show |
T | 1 | a0002c0002t0001g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.661+3349_661+3366d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | ||||||
chr17:47351298 | TGTGTGTG others(15): Show |
T | 8 | a0002c0002t0001g0056 a0002c0002t0001g0298 a0002c0002t0001g0309 others(5): Show |
8 | HG00673.hp1 HG01106.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.661+3349_661+3370d others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | ||||||
chr17:47351300 | T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3349T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351300 | |||||||
chr17:47351300 | TGTGTGCG others(9): Show |
T | 6 | a0002c0002t0001g0259 a0002c0002t0001g0294 a0002c0002t0001g0312 others(3): Show |
6 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.661+3351_661+3366d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351300 | ||||||
chr17:47351302 | T | C | 3 | a0002c0002t0001g0290 a0002c0002t0001g0293 a0002c0002t0001g0325 |
3 | HG01192.hp2 HG03492.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.661+3351T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351302 | |||||||
chr17:47351302 | TGTGCGCG others(9): Show |
T | 2 | a0002c0002t0001g0279 a0002c0002t0001g0347 |
2 | HG02004.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661+3353_661+3368d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351302 | ||||||
chr17:47351304 | T | C | 12 | a0002c0002t0001g0262 a0002c0002t0001g0283 a0002c0002t0001g0290 others(9): Show |
12 | HG01192.hp2 HG02895.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+3353T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351304 | |||||||
chr17:47351304 | T | TGCGC | 3 | a0002c0002t0001g0010 a0002c0002t0001g0349 a0002c0010t0001g0268 |
3 | HG03540.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.661+3374_661+3377d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(7): Show |
1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(21): Show |
1 | a0002c0002t0003g0338 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(30): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(11): Show |
1 | a0002c0002t0003g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.661+3354_661+3355i others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(13): Show |
1 | a0002c0002t0003g0057 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(15): Show |
2 | a0002c0002t0003g0284 a0002c0002t0003g0331 |
2 | HG00741.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.661+3354_661+3355i others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(25): Show |
1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.661+3354_661+3355i others(34): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | T | TGTGTGTG others(19): Show |
1 | a0002c0002t0003g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351304 | TGCGCGCG others(5): Show |
T | 2 | a0002c0002t0001g0263 a0002c0002t0001g0278 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.661+3366_661+3377d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | ||||||
chr17:47351306 | C | T | 201 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(198): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.661+3355C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351306 | |||||||
chr17:47351308 | C | CGT | 5 | a0003c0004t0002g0222 a0003c0004t0002g0233 a0003c0004t0002g0234 others(2): Show |
5 | NA18942.hp1 NA18946.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3358_661+3359i others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351308 | ||||||
chr17:47351308 | C | CGTGT | 5 | a0003c0004t0001g0141 a0003c0004t0002g0230 a0003c0004t0002g0245 others(2): Show |
5 | HG01515.hp2 HG02056.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3358_661+3359i others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351308 | ||||||
chr17:47351308 | C | T | 227 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(224): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.661+3357C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351308 | |||||||
chr17:47351310 | C | T | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.661+3359C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351310 | |||||||
chr17:47351312 | C | T | 214 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
218 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.661+3361C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351312 | |||||||
chr17:47351313 | G | T | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+3362G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351313 | |||||||
chr17:47351314 | C | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+3363C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351314 | |||||||
chr17:47351314 | C | T | 145 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(142): Show |
145 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.661+3363C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351314 | |||||||
chr17:47351316 | C | T | 97 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(94): Show |
97 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.661+3365C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351316 | |||||||
chr17:47351317 | G | A | 2 | a0002c0002t0003g0335 a0002c0002t0003g0338 |
2 | HG01069.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.661+3366G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351317 | |||||||
chr17:47351318 | C | T | 4 | a0001c0001t0001g0124 a0002c0002t0001g0278 a0003c0008t0001g0006 others(1): Show |
4 | HG01243.hp2 HG03195.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+3367C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351318 | |||||||
chr17:47351323 | G | A | 1 | a0005c0005t0001g0207 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.661+3372G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351323 | |||||||
chr17:47351327 | G | A | 7 | a0001c0022t0001g0194 a0002c0002t0003g0055 a0002c0002t0003g0057 others(4): Show |
7 | HG00323.hp2 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+3376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351327 | |||||||
chr17:47351591 | T | C | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.661+3640T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351591 | |||||||
chr17:47351659 | T | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.661+3708T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351659 | |||||||
chr17:47351808 | T | G | 1 | a0002c0002t0001g0321 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.661+3857T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351808 | |||||||
chr17:47351848 | A | ATTCTTTG others(20): Show |
1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+3919_661+3920i others(29): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351848 | ||||||
chr17:47351895 | T | C | 1 | a0002c0002t0001g0304 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.661+3944T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351895 | |||||||
chr17:47351899 | G | GT | 78 | a0001c0001t0001g0088 a0001c0001t0001g0139 a0001c0001t0001g0152 others(75): Show |
81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+3969dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | ||||||
chr17:47351899 | GT | G | 6 | a0001c0001t0001g0120 a0001c0001t0005g0256 a0001c0013t0001g0196 others(3): Show |
6 | HG01070.hp1 HG02056.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+3969delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | ||||||
chr17:47351899 | GTT | G | 38 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(35): Show |
39 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+3968_661+3969d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | ||||||
chr17:47351902 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.661+3951T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351902 | |||||||
chr17:47352058 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.661+4107C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352058 | |||||||
chr17:47352065 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+4114C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352065 | |||||||
chr17:47352096 | G | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+4145G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352096 | |||||||
chr17:47352104 | G | A | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.661+4153G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352104 | |||||||
chr17:47352181 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+4230C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352181 | |||||||
chr17:47352183 | C | T | 43 | a0001c0001t0001g0084 a0001c0001t0001g0176 a0003c0004t0001g0141 others(40): Show |
44 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.661+4232C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352183 | |||||||
chr17:47352248 | C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+4297C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352248 | |||||||
chr17:47352359 | C | T | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+4408C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352359 | |||||||
chr17:47352365 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661+4414A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352365 | |||||||
chr17:47352410 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+4459A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352410 | |||||||
chr17:47352411 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+4460G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352411 | |||||||
chr17:47352449 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.661+4498A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352449 | |||||||
chr17:47352569 | G | T | 1 | a0002c0002t0001g0330 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.661+4618G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352569 | |||||||
chr17:47352722 | A | G | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+4771A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352722 | |||||||
chr17:47352797 | A | C | 37 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.661+4846A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352797 | |||||||
chr17:47353168 | A | G | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.661+5217A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353168 | |||||||
chr17:47353200 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+5249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353200 | |||||||
chr17:47353296 | A | T | 1 | a0005c0005t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.661+5345A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353296 | |||||||
chr17:47353389 | G | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.661+5438G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353389 | |||||||
chr17:47353497 | T | G | 3 | a0002c0002t0003g0331 a0002c0002t0003g0335 a0002c0002t0003g0338 |
3 | HG01069.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.661+5546T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353497 | |||||||
chr17:47353539 | G | A | 8 | a0002c0002t0001g0259 a0002c0002t0001g0279 a0002c0002t0001g0294 others(5): Show |
8 | HG00738.hp2 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+5588G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353539 | |||||||
chr17:47353632 | G | A | 1 | a0002c0002t0001g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.661+5681G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353632 | |||||||
chr17:47353696 | A | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+5745A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353696 | |||||||
chr17:47353868 | A | G | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.661+5917A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353868 | |||||||
chr17:47353877 | T | C | 1 | a0002c0002t0001g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.661+5926T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353877 | |||||||
chr17:47354188 | G | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+6237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354188 | |||||||
chr17:47354483 | C | T | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661+6532C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354483 | |||||||
chr17:47354534 | A | T | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6583A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354534 | |||||||
chr17:47354535 | T | A | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6584T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354535 | |||||||
chr17:47354535 | T | G | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.661+6584T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354535 | |||||||
chr17:47354536 | A | T | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6585A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354536 | |||||||
chr17:47354550 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.661+6599C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354550 | |||||||
chr17:47354569 | G | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.661+6618G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354569 | |||||||
chr17:47354580 | C | T | 1 | a0007c0009t0002g0247 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.661+6629C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354580 | |||||||
chr17:47354640 | C | A | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.661+6689C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354640 | |||||||
chr17:47354705 | C | T | 1 | a0005c0005t0003g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-6673C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354705 | |||||||
chr17:47354775 | G | C | 1 | a0002c0002t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.662-6603G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354775 | |||||||
chr17:47354847 | G | A | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.662-6531G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354847 | |||||||
chr17:47354859 | C | A | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.662-6519C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354859 | |||||||
chr17:47355087 | A | T | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.662-6291A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355087 | |||||||
chr17:47355112 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.662-6266G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355112 | |||||||
chr17:47355226 | G | C | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.662-6152G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355226 | |||||||
chr17:47355252 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.662-6126A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355252 | |||||||
chr17:47355314 | G | T | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-6064G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355314 | |||||||
chr17:47355512 | C | T | 2 | a0003c0004t0002g0224 a0003c0004t0002g0251 |
2 | NA18964.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.662-5866C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355512 | |||||||
chr17:47355517 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-5861A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355517 | |||||||
chr17:47355539 | C | G | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.662-5839C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355539 | |||||||
chr17:47355540 | G | C | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.662-5838G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355540 | |||||||
chr17:47355554 | C | T | 3 | a0002c0002t0003g0284 a0002c0002t0003g0315 a0002c0002t0003g0324 |
3 | HG00323.hp2 HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.662-5824C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355554 | |||||||
chr17:47355570 | A | AT | 49 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(46): Show |
52 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.662-5787dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47355570 | ||||||
chr17:47355570 | AT | A | 49 | a0001c0001t0001g0082 a0001c0015t0001g0106 a0002c0002t0001g0303 others(46): Show |
50 | HG00438.hp2 HG00544.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.662-5787delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47355570 | ||||||
chr17:47355605 | G | A | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.662-5773G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355605 | |||||||
chr17:47355728 | A | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-5650A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355728 | |||||||
chr17:47355856 | C | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-5522C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355856 | |||||||
chr17:47356104 | CT | C | 41 | a0002c0002t0001g0303 a0003c0004t0001g0141 a0003c0004t0002g0109 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-5263delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47356104 | ||||||
chr17:47356141 | G | A | 1 | a0006c0007t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.662-5237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356141 | |||||||
chr17:47356300 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-5078A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356300 | |||||||
chr17:47356594 | G | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.662-4784G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356594 | |||||||
chr17:47356605 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.662-4773C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356605 | |||||||
chr17:47356631 | G | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-4747G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356631 | |||||||
chr17:47356722 | A | G | 2 | a0001c0013t0001g0196 a0001c0013t0001g0197 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.662-4656A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356722 | |||||||
chr17:47357043 | C | T | 2 | a0002c0002t0001g0283 a0002c0002t0008g0323 |
2 | HG03669.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.662-4335C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357043 | |||||||
chr17:47357082 | C | T | 7 | a0001c0001t0001g0122 a0002c0010t0001g0265 a0002c0010t0001g0267 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-4296C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357082 | |||||||
chr17:47357104 | T | C | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.662-4274T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357104 | |||||||
chr17:47357196 | C | CTGTT | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4179_662-4178i others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47357196 | ||||||
chr17:47357405 | C | T | 1 | a0002c0002t0001g0296 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.662-3973C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357405 | |||||||
chr17:47357667 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-3711G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357667 | |||||||
chr17:47357882 | C | T | 1 | a0004c0003t0001g0031 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.662-3496C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357882 | |||||||
chr17:47357989 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.662-3389G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357989 | |||||||
chr17:47358193 | T | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.662-3185T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358193 | |||||||
chr17:47358209 | A | G | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-3169A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358209 | |||||||
chr17:47358884 | A | G | 2 | a0003c0008t0001g0006 a0003c0008t0004g0005 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.662-2494A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358884 | |||||||
chr17:47358941 | T | C | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-2437T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358941 | |||||||
chr17:47358956 | T | G | 2 | a0001c0013t0001g0196 a0001c0013t0001g0197 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.662-2422T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358956 | |||||||
chr17:47359119 | G | A | 1 | a0002c0002t0001g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.662-2259G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359119 | |||||||
chr17:47359149 | A | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.662-2229A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359149 | |||||||
chr17:47359190 | G | A | 7 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 others(4): Show |
7 | HG02647.hp2 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-2188G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359190 | |||||||
chr17:47359283 | G | A | 8 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(5): Show |
8 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.662-2095G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359283 | |||||||
chr17:47359492 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0052 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.662-1886G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359492 | |||||||
chr17:47359517 | G | GT | 95 | a0001c0001t0001g0136 a0002c0002t0001g0002 a0002c0002t0001g0056 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.662-1846dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359517 | ||||||
chr17:47359517 | GT | G | 91 | a0001c0001t0001g0147 a0003c0004t0001g0141 a0003c0004t0002g0109 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.662-1846delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359517 | ||||||
chr17:47359575 | A | C | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.662-1803A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359575 | |||||||
chr17:47359591 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.662-1787C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359591 | |||||||
chr17:47359621 | AT | A | 92 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1747delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359621 | ||||||
chr17:47359751 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1627A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359751 | |||||||
chr17:47359880 | G | A | 1 | a0002c0002t0003g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.662-1498G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359880 | |||||||
chr17:47360050 | G | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1328G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360050 | |||||||
chr17:47360107 | G | A | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.662-1271G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360107 | |||||||
chr17:47360145 | A | G | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-1233A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360145 | |||||||
chr17:47360178 | C | G | 2 | a0007c0009t0002g0218 a0007c0009t0002g0247 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.662-1200C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360178 | |||||||
chr17:47360255 | G | A | 17 | a0001c0001t0001g0052 a0001c0001t0005g0255 a0001c0001t0005g0256 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-1123G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360255 | |||||||
chr17:47360360 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-1018A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360360 | |||||||
chr17:47360381 | T | G | 100 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(97): Show |
104 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.662-997T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360381 | |||||||
chr17:47360617 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-761C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360617 | |||||||
chr17:47360623 | A | G | 1 | a0002c0002t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.662-755A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360623 | |||||||
chr17:47360645 | C | A | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.662-733C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360645 | |||||||
chr17:47360696 | C | T | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.662-682C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360696 | |||||||
chr17:47360971 | T | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-407T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360971 | |||||||
chr17:47361000 | GTTTAA | G | 17 | a0001c0001t0001g0052 a0001c0001t0005g0255 a0001c0001t0005g0256 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-373_662-369del others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47361000 | ||||||
chr17:47361047 | T | C | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.662-331T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361047 | |||||||
chr17:47361051 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-327A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361051 | |||||||
chr17:47361149 | T | C | 38 | a0003c0008t0001g0134 a0004c0003t0001g0001 a0004c0003t0001g0003 others(35): Show |
41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.662-229T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361149 | |||||||
chr17:47361216 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.662-162T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361216 | |||||||
chr17:47361231 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-147A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361231 | |||||||
chr17:47361324 | G | C | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-54G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361324 | |||||||
chr17:47361520 | CAGTG | C | 138 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
splice_region_variant&intron_variant | LOW | c.805+3_805+6delGAGT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47361520 | ||||||
chr17:47361586 | C | T | 120 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
120 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(117): Show |
intron_variant | MODIFIER | c.805+65C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47361586 | |||||||
chr17:47361916 | C | T | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+395C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47361916 | |||||||
chr17:47362195 | A | C | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+674A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362195 | |||||||
chr17:47362389 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.805+868C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362389 | |||||||
chr17:47362510 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.805+989C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362510 | |||||||
chr17:47362674 | G | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805+1153G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362674 | |||||||
chr17:47362707 | C | A | 1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+1186C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362707 | |||||||
chr17:47362801 | C | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1280C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362801 | |||||||
chr17:47362857 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.805+1336C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362857 | |||||||
chr17:47362891 | A | G | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.805+1370A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362891 | |||||||
chr17:47362903 | C | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.805+1382C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362903 | |||||||
chr17:47362929 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+1408C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362929 | |||||||
chr17:47362930 | A | G | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1409A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362930 | |||||||
chr17:47362937 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+1416G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362937 | |||||||
chr17:47362961 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.805+1440G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362961 | |||||||
chr17:47363019 | C | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.805+1498C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363019 | |||||||
chr17:47363025 | C | T | 1 | a0002c0002t0001g0309 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.805+1504C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363025 | |||||||
chr17:47363035 | G | C | 2 | a0003c0004t0002g0222 a0003c0004t0002g0230 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.805+1514G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363035 | |||||||
chr17:47363126 | C | T | 5 | a0001c0001t0001g0081 a0003c0008t0001g0134 a0004c0003t0001g0065 others(2): Show |
5 | HG02559.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+1605C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363126 | |||||||
chr17:47363261 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805+1740C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363261 | |||||||
chr17:47363462 | C | CT | 11 | a0001c0001t0001g0135 a0001c0001t0001g0190 a0003c0008t0001g0006 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+1957dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47363462 | ||||||
chr17:47363462 | CT | C | 56 | a0001c0001t0001g0119 a0002c0002t0001g0281 a0002c0002t0001g0295 others(53): Show |
57 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.805+1957delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47363462 | ||||||
chr17:47363490 | C | T | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1969C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363490 | |||||||
chr17:47363520 | G | A | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.805+1999G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363520 | |||||||
chr17:47363535 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.805+2014C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363535 | |||||||
chr17:47363537 | A | T | 6 | a0004c0003t0001g0001 a0004c0003t0001g0025 a0004c0003t0001g0026 others(3): Show |
8 | NA18944.hp2 NA18964.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+2016A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363537 | |||||||
chr17:47363582 | T | C | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.805+2061T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363582 | |||||||
chr17:47363754 | A | T | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.805+2233A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363754 | |||||||
chr17:47363799 | A | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+2278A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363799 | |||||||
chr17:47363858 | C | T | 14 | a0003c0004t0002g0214 a0003c0004t0002g0216 a0003c0004t0002g0219 others(11): Show |
15 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.805+2337C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363858 | |||||||
chr17:47363956 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.805+2435A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363956 | |||||||
chr17:47364120 | G | A | 92 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(89): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+2599G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364120 | |||||||
chr17:47364349 | C | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.805+2828C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364349 | |||||||
chr17:47364409 | G | A | 5 | a0002c0002t0001g0259 a0002c0002t0001g0279 a0002c0002t0001g0294 others(2): Show |
5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+2888G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364409 | |||||||
chr17:47364438 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0056 a0002c0002t0001g0259 others(50): Show |
55 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.805+2917G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364438 | |||||||
chr17:47364459 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+2938C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364459 | |||||||
chr17:47364478 | A | C | 1 | a0004c0003t0001g0021 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+2957A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364478 | |||||||
chr17:47364513 | A | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+2992A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364513 | |||||||
chr17:47364591 | G | A | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.805+3070G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364591 | |||||||
chr17:47364598 | A | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.805+3077A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364598 | |||||||
chr17:47364683 | G | A | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.805+3162G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364683 | |||||||
chr17:47364997 | C | T | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.805+3476C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364997 | |||||||
chr17:47365087 | T | C | 2 | a0003c0008t0004g0011 a0003c0008t0004g0012 |
2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.805+3566T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365087 | |||||||
chr17:47365097 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.805+3576C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365097 | |||||||
chr17:47365237 | C | T | 1 | a0003c0008t0004g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.805+3716C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365237 | |||||||
chr17:47365238 | G | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+3717G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365238 | |||||||
chr17:47365356 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.805+3835G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365356 | |||||||
chr17:47365458 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.805+3937T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365458 | |||||||
chr17:47365474 | G | A | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+3953G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365474 | |||||||
chr17:47365525 | C | T | 1 | a0005c0005t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.805+4004C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365525 | |||||||
chr17:47365831 | CAA | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.805+4312_805+4313d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47365831 | ||||||
chr17:47366032 | A | G | 1 | a0002c0002t0001g0330 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806-4405A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366032 | |||||||
chr17:47366128 | A | G | 138 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.806-4309A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366128 | |||||||
chr17:47366137 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.806-4300A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366137 | |||||||
chr17:47366298 | C | G | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.806-4139C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366298 | |||||||
chr17:47366314 | G | GT | 62 | a0001c0001t0001g0175 a0001c0006t0001g0094 a0001c0006t0001g0095 others(59): Show |
63 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.806-4109dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47366314 | ||||||
chr17:47366314 | GT | G | 10 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 others(7): Show |
10 | HG02615.hp1 HG02717.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-4109delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47366314 | ||||||
chr17:47366372 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806-4065G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366372 | |||||||
chr17:47366462 | G | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.806-3975G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366462 | |||||||
chr17:47366674 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.806-3763G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366674 | |||||||
chr17:47366707 | A | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.806-3730A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366707 | |||||||
chr17:47366723 | C | T | 1 | a0004c0003t0001g0036 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.806-3714C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366723 | |||||||
chr17:47366800 | T | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.806-3637T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366800 | |||||||
chr17:47366923 | T | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.806-3514T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366923 | |||||||
chr17:47367245 | C | T | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-3192C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367245 | |||||||
chr17:47367502 | G | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-2935G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367502 | |||||||
chr17:47367531 | G | A | 2 | a0001c0001t0005g0255 a0001c0001t0005g0257 |
2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806-2906G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367531 | |||||||
chr17:47367656 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-2781G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367656 | |||||||
chr17:47367811 | G | A | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.806-2626G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367811 | |||||||
chr17:47367835 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.806-2602G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367835 | |||||||
chr17:47367863 | C | T | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.806-2574C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367863 | |||||||
chr17:47368074 | T | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-2363T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368074 | |||||||
chr17:47368435 | C | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG01169.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.806-2002C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368435 | |||||||
chr17:47368453 | T | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0198 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.806-1984T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368453 | |||||||
chr17:47368517 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.806-1920A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368517 | |||||||
chr17:47368792 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-1645A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368792 | |||||||
chr17:47368886 | G | T | 6 | a0007c0009t0001g0221 a0007c0009t0002g0218 a0007c0009t0002g0235 others(3): Show |
6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.806-1551G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368886 | |||||||
chr17:47369113 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.806-1324C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369113 | |||||||
chr17:47369137 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.806-1300A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369137 | |||||||
chr17:47369163 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.806-1274C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369163 | |||||||
chr17:47369163 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1274C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369163 | |||||||
chr17:47369288 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.806-1149T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369288 | |||||||
chr17:47369358 | G | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1079G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369358 | |||||||
chr17:47369392 | A | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.806-1045A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369392 | |||||||
chr17:47369579 | C | T | 1 | a0002c0002t0001g0332 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.806-858C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369579 | |||||||
chr17:47369694 | T | A | 3 | a0002c0002t0003g0331 a0002c0002t0003g0335 a0002c0002t0003g0338 |
3 | HG01069.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.806-743T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369694 | |||||||
chr17:47370238 | A | G | 2 | a0001c0001t0001g0129 a0003c0008t0001g0134 |
2 | NA18960.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.806-199A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370238 | |||||||
chr17:47370268 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-169C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370268 | |||||||
chr17:47370368 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | HG01433.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.806-69A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370368 | |||||||
chr17:47370436 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
splice_acceptor_variant&intron_variant | HIGH | c.806-1G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370436 | |||||||
chr17:47370715 | G | GT | 14 | a0003c0004t0002g0239 a0006c0007t0001g0059 a0006c0007t0001g0060 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.877+213dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370715 | ||||||
chr17:47370722 | G | T | 55 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(52): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.877+214G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370722 | |||||||
chr17:47370738 | GT | G | 175 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(172): Show |
176 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.877+250delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370738 | ||||||
chr17:47370738 | GTT | G | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.877+249_877+250del others(2): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370738 | ||||||
chr17:47370742 | T | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0139 others(3): Show |
6 | HG02965.hp2 HG03540.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+234T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370742 | |||||||
chr17:47370743 | T | G | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
133 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.877+235T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370743 | |||||||
chr17:47370746 | T | G | 2 | a0001c0001t0005g0255 a0001c0001t0005g0257 |
2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.877+238T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370746 | |||||||
chr17:47370747 | T | G | 2 | a0001c0001t0001g0155 a0001c0001t0005g0256 |
2 | HG02738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.877+239T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370747 | |||||||
chr17:47370748 | T | G | 1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.877+240T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370748 | |||||||
chr17:47370749 | T | G | 1 | a0001c0006t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.877+241T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370749 | |||||||
chr17:47370908 | G | A | 1 | a0002c0002t0003g0055 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.877+400G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370908 | |||||||
chr17:47371032 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.877+524G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371032 | |||||||
chr17:47371062 | G | GT | 23 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0001c0001t0001g0108 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.877+575dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371062 | ||||||
chr17:47371062 | G | T | 8 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0198 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.877+554G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371062 | |||||||
chr17:47371062 | GT | G | 101 | a0001c0001t0001g0174 a0001c0001t0001g0180 a0001c0015t0001g0106 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.877+575delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371062 | ||||||
chr17:47371064 | T | TG | 35 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.877+556_877+557ins others(1): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371064 | |||||||
chr17:47371070 | T | C | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.877+562T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371070 | |||||||
chr17:47371249 | G | T | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.877+741G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371249 | |||||||
chr17:47371407 | A | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+899A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371407 | |||||||
chr17:47371654 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 |
3 | HG00673.hp2 HG02523.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.877+1146C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371654 | |||||||
chr17:47371806 | G | T | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877+1298G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371806 | |||||||
chr17:47371915 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.877+1407C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371915 | |||||||
chr17:47371915 | CTG | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.877+1411_877+1412d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371915 | ||||||
chr17:47371967 | T | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+1459T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371967 | |||||||
chr17:47372124 | A | G | 37 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.877+1616A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372124 | |||||||
chr17:47372746 | A | AAT | 6 | a0002c0010t0001g0265 a0002c0010t0001g0267 a0002c0010t0001g0268 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-1720_878-1719d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47372746 | ||||||
chr17:47372761 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.878-1711C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372761 | |||||||
chr17:47372921 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.878-1551A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372921 | |||||||
chr17:47373017 | CT | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.878-1452delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47373017 | ||||||
chr17:47373041 | T | C | 1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-1431T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373041 | |||||||
chr17:47373054 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.878-1418A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373054 | |||||||
chr17:47373273 | T | C | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.878-1199T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373273 | |||||||
chr17:47373819 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.878-653C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373819 | |||||||
chr17:47373837 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.878-635G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373837 | |||||||
chr17:47373845 | G | A | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.878-627G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373845 | |||||||
chr17:47374084 | T | A | 1 | a0002c0002t0001g0321 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.878-388T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374084 | |||||||
chr17:47374139 | A | G | 1 | a0006c0007t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.878-333A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374139 | |||||||
chr17:47374156 | A | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.878-316A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374156 | |||||||
chr17:47375304 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1372+338T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375304 | |||||||
chr17:47375327 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1372+361G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375327 | |||||||
chr17:47375483 | CG | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+522delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47375483 | ||||||
chr17:47375493 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1372+527A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375493 | |||||||
chr17:47375565 | C | T | 2 | a0002c0002t0001g0296 a0002c0002t0001g0302 |
2 | NA19010.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1372+599C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375565 | |||||||
chr17:47375767 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+801C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375767 | |||||||
chr17:47375830 | G | C | 1 | a0002c0002t0001g0298 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1372+864G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375830 | |||||||
chr17:47375915 | A | G | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1372+949A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375915 | |||||||
chr17:47375992 | T | C | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372+1026T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375992 | |||||||
chr17:47376216 | G | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1372+1250G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376216 | |||||||
chr17:47376339 | T | TG | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+1375dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47376339 | ||||||
chr17:47376550 | TG | T | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-1215delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376550 | |||||||
chr17:47376551 | G | C | 1 | a0002c0002t0001g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1373-1215G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376551 | |||||||
chr17:47376579 | A | G | 1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1373-1187A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376579 | |||||||
chr17:47376584 | T | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1373-1182T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376584 | |||||||
chr17:47376885 | T | C | 3 | a0003c0004t0002g0220 a0003c0004t0002g0226 a0003c0004t0002g0227 |
3 | NA18945.hp1 NA18984.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1373-881T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376885 | |||||||
chr17:47377186 | A | AAC | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1373-565_1373-564d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47377186 | ||||||
chr17:47377204 | C | T | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1373-562C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377204 | |||||||
chr17:47377213 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1373-553A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377213 | |||||||
chr17:47377349 | A | G | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-417A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377349 | |||||||
chr17:47377361 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1373-405C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377361 | |||||||
chr17:47377438 | A | T | 6 | a0007c0009t0001g0221 a0007c0009t0002g0218 a0007c0009t0002g0235 others(3): Show |
6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-328A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377438 | |||||||
chr17:47377517 | G | A | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1373-249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377517 | |||||||
chr17:47377566 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1373-200G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377566 | |||||||
chr17:47378089 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1510+186A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378089 | |||||||
chr17:47378107 | G | A | 238 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(235): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1510+204G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378107 | |||||||
chr17:47378203 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1510+300G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378203 | |||||||
chr17:47378216 | C | T | 334 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1510+313C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378216 | |||||||
chr17:47378237 | G | T | 2 | a0005c0005t0001g0204 a0005c0005t0001g0205 |
2 | HG03834.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1510+334G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378237 | |||||||
chr17:47378257 | A | C | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1510+354A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378257 | |||||||
chr17:47378303 | G | A | 3 | a0002c0002t0003g0055 a0002c0002t0003g0057 a0002c0002t0003g0058 |
3 | HG01255.hp1 HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1510+400G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378303 | |||||||
chr17:47378304 | G | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1510+401G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378304 | |||||||
chr17:47378322 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1510+419A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378322 | |||||||
chr17:47378342 | A | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+439A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378342 | |||||||
chr17:47378727 | A | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1511-455A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378727 | |||||||
chr17:47378734 | A | G | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1511-448A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378734 | |||||||
chr17:47378831 | A | C | 1 | a0002c0002t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1511-351A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378831 | |||||||
chr17:47378967 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1511-215G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378967 | |||||||
chr17:47378984 | T | G | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1511-198T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378984 | |||||||
chr17:47378996 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1511-186T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378996 | |||||||
chr17:47379094 | A | C | 50 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1511-88A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47379094 | |||||||
chr17:47379279 | G | T | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582+26G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379279 | |||||||
chr17:47379365 | ACT | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+115_1582+116d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47379365 | ||||||
chr17:47379476 | A | T | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1582+223A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379476 | |||||||
chr17:47379545 | T | C | 37 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1582+292T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379545 | |||||||
chr17:47379562 | TG | T | 128 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1582+310delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379562 | |||||||
chr17:47379563 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0001c0001t0001g0133 others(5): Show |
8 | HG00735.hp1 HG01175.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+310G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379563 | |||||||
chr17:47379639 | G | A | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1582+386G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379639 | |||||||
chr17:47379691 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1582+438T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379691 | |||||||
chr17:47379726 | A | C | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1582+473A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379726 | |||||||
chr17:47379736 | G | T | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1582+483G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379736 | |||||||
chr17:47379770 | A | AT | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.1582+523dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47379770 | ||||||
chr17:47379922 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1582+669T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379922 | |||||||
chr17:47380000 | G | T | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1582+747G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380000 | |||||||
chr17:47380037 | C | T | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1582+784C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380037 | |||||||
chr17:47380100 | C | CT | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+850dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380100 | ||||||
chr17:47380349 | C | T | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1582+1096C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380349 | |||||||
chr17:47380366 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1582+1113T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380366 | |||||||
chr17:47380441 | T | C | 1 | a0002c0002t0001g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1582+1188T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380441 | |||||||
chr17:47380544 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1582+1291T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380544 | |||||||
chr17:47380693 | C | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1582+1440C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380693 | |||||||
chr17:47380715 | A | G | 1 | a0005c0005t0002g0225 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1582+1462A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380715 | |||||||
chr17:47380769 | A | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+1516A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380769 | |||||||
chr17:47380876 | T | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1582+1623T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380876 | |||||||
chr17:47380880 | C | CT | 28 | a0001c0001t0001g0051 a0001c0001t0001g0151 a0001c0001t0005g0257 others(25): Show |
28 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1582+1647dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | ||||||
chr17:47380880 | C | CTT | 49 | a0001c0006t0001g0100 a0003c0004t0001g0141 a0003c0004t0002g0109 others(46): Show |
50 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1582+1646_1582+164 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | ||||||
chr17:47380880 | C | CTTTT | 34 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(31): Show |
37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1582+1644_1582+164 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | ||||||
chr17:47381098 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+1845G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381098 | |||||||
chr17:47381180 | T | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+1927T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381180 | |||||||
chr17:47381202 | G | GT | 35 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1582+1958dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47381202 | ||||||
chr17:47381892 | G | GA | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+2642dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47381892 | ||||||
chr17:47381909 | T | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1582+2656T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381909 | |||||||
chr17:47382052 | T | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+2799T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382052 | |||||||
chr17:47382211 | C | T | 3 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 |
3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1582+2958C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382211 | |||||||
chr17:47382240 | C | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1582+2987C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382240 | |||||||
chr17:47382330 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1582+3077T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382330 | |||||||
chr17:47382372 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1582+3119G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382372 | |||||||
chr17:47382647 | G | A | 5 | a0002c0002t0001g0259 a0002c0002t0001g0279 a0002c0002t0001g0294 others(2): Show |
5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1582+3394G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382647 | |||||||
chr17:47382786 | T | C | 2 | a0006c0007t0001g0059 a0006c0007t0001g0062 |
2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1582+3533T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382786 | |||||||
chr17:47382813 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+3560G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382813 | |||||||
chr17:47382823 | C | T | 238 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(235): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1582+3570C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382823 | |||||||
chr17:47382847 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1582+3594C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382847 | |||||||
chr17:47383242 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1582+3989A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383242 | |||||||
chr17:47383463 | G | A | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4210G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383463 | |||||||
chr17:47383497 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1582+4244T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383497 | |||||||
chr17:47383526 | T | C | 1 | a0002c0002t0001g0306 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1582+4273T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383526 | |||||||
chr17:47383716 | T | C | 1 | a0003c0004t0002g0231 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1582+4463T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383716 | |||||||
chr17:47383805 | T | C | 1 | a0005c0005t0001g0007 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1582+4552T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383805 | |||||||
chr17:47384011 | C | T | 1 | a0001c0015t0001g0192 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1582+4758C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384011 | |||||||
chr17:47384017 | A | G | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1582+4764A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384017 | |||||||
chr17:47384020 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1582+4767C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384020 | |||||||
chr17:47384083 | G | A | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1582+4830G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384083 | |||||||
chr17:47384095 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0153 |
2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1582+4842C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384095 | |||||||
chr17:47384120 | TCA | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+4870_1582+487 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384120 | ||||||
chr17:47384143 | CA | C | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4891delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384143 | |||||||
chr17:47384144 | A | G | 51 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(48): Show |
54 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1582+4891A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384144 | |||||||
chr17:47384145 | G | GT | 38 | a0001c0001t0001g0132 a0001c0001t0001g0275 a0004c0003t0001g0001 others(35): Show |
41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4904dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384145 | ||||||
chr17:47384145 | GT | G | 15 | a0001c0001t0005g0255 a0001c0001t0005g0257 a0001c0006t0001g0093 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1582+4904delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384145 | ||||||
chr17:47384146 | T | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4893T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384146 | |||||||
chr17:47384154 | T | G | 1 | a0006c0007t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1582+4901T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384154 | |||||||
chr17:47384157 | T | G | 1 | a0007c0009t0002g0248 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1582+4904T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384157 | |||||||
chr17:47384158 | G | GT | 7 | a0001c0001t0001g0136 a0002c0002t0001g0300 a0002c0002t0001g0303 others(4): Show |
7 | HG00438.hp1 HG03927.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582+4918dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384158 | ||||||
chr17:47384158 | G | T | 16 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0006c0007t0001g0059 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1582+4905G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384158 | |||||||
chr17:47384159 | T | G | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG02135.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+4906T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384159 | |||||||
chr17:47384165 | T | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+4912T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384165 | |||||||
chr17:47384223 | G | A | 1 | a0003c0004t0002g0245 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1582+4970G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384223 | |||||||
chr17:47384340 | C | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+5087C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384340 | |||||||
chr17:47384426 | G | GT | 6 | a0001c0001t0001g0083 a0001c0001t0001g0119 a0001c0001t0001g0132 others(3): Show |
6 | HG00735.hp1 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582+5185dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384426 | ||||||
chr17:47384449 | G | GTATTAAG others(13): Show |
1 | a0006c0007t0001g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1582+5214_1582+523 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384449 | ||||||
chr17:47384488 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+5235C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384488 | |||||||
chr17:47384558 | G | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1582+5305G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384558 | |||||||
chr17:47384629 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1582+5376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384629 | |||||||
chr17:47384667 | C | A | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1582+5414C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384667 | |||||||
chr17:47384789 | GAGA | G | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+5539_1582+554 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384789 | ||||||
chr17:47385006 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+5753T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385006 | |||||||
chr17:47385022 | C | T | 4 | a0005c0005t0001g0110 a0005c0005t0001g0116 a0005c0005t0001g0202 others(1): Show |
4 | NA18981.hp2 NA19000.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+5769C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385022 | |||||||
chr17:47385095 | G | A | 1 | a0005c0005t0003g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1582+5842G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385095 | |||||||
chr17:47385203 | G | A | 3 | a0002c0002t0001g0307 a0002c0002t0001g0314 a0002c0002t0009g0313 |
3 | NA18961.hp1 NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1582+5950G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385203 | |||||||
chr17:47385507 | T | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-5930T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385507 | |||||||
chr17:47385522 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1583-5915G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385522 | |||||||
chr17:47385636 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-5801C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385636 | |||||||
chr17:47385760 | G | T | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1583-5677G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385760 | |||||||
chr17:47385801 | G | C | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1583-5636G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385801 | |||||||
chr17:47385852 | T | C | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1583-5585T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385852 | |||||||
chr17:47385875 | A | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1583-5562A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385875 | |||||||
chr17:47385891 | T | C | 1 | a0002c0002t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1583-5546T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385891 | |||||||
chr17:47386285 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1583-5152G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386285 | |||||||
chr17:47386473 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-4964T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386473 | |||||||
chr17:47386476 | C | T | 29 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0091 others(26): Show |
29 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1583-4961C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386476 | |||||||
chr17:47386642 | A | C | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1583-4795A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386642 | |||||||
chr17:47386653 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4784G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386653 | |||||||
chr17:47386770 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1583-4667G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386770 | |||||||
chr17:47386891 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1583-4546C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386891 | |||||||
chr17:47387021 | C | T | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4416C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387021 | |||||||
chr17:47387161 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-4276G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387161 | |||||||
chr17:47387309 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1583-4128A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387309 | |||||||
chr17:47387311 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-4126T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387311 | |||||||
chr17:47387405 | T | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4032T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387405 | |||||||
chr17:47387577 | A | G | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1583-3860A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387577 | |||||||
chr17:47387601 | A | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1583-3836A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387601 | |||||||
chr17:47387636 | C | CTT | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3801_1583-380 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387636 | |||||||
chr17:47387639 | T | TAA | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3798_1583-379 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387639 | |||||||
chr17:47387641 | C | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3796C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387641 | |||||||
chr17:47387643 | G | GGAT | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3794_1583-379 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387643 | |||||||
chr17:47387645 | C | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3792C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387645 | |||||||
chr17:47387649 | T | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3788T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387649 | |||||||
chr17:47387661 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1583-3776A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387661 | |||||||
chr17:47387922 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1583-3515T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387922 | |||||||
chr17:47388369 | A | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-3068A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388369 | |||||||
chr17:47388468 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-2969T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388468 | |||||||
chr17:47388543 | T | C | 7 | a0003c0008t0001g0006 a0003c0008t0004g0005 a0003c0008t0004g0011 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1583-2894T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388543 | |||||||
chr17:47388577 | C | T | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-2860C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388577 | |||||||
chr17:47388719 | T | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1583-2718T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388719 | |||||||
chr17:47388915 | AT | A | 52 | a0003c0008t0001g0006 a0004c0003t0001g0001 a0004c0003t0001g0003 others(49): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1583-2511delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47388915 | ||||||
chr17:47388915 | ATTTT | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-2514_1583-251 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47388915 | ||||||
chr17:47389099 | CA | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-2337delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389099 | |||||||
chr17:47389248 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1583-2189G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389248 | |||||||
chr17:47389405 | C | T | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1583-2032C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389405 | |||||||
chr17:47389508 | G | A | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-1929G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389508 | |||||||
chr17:47389578 | C | CT | 50 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0111 others(47): Show |
51 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1583-1841dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389578 | ||||||
chr17:47389578 | C | CTT | 8 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(5): Show |
8 | HG00408.hp1 HG02135.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1583-1842_1583-184 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389578 | ||||||
chr17:47389596 | T | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1583-1841T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389596 | |||||||
chr17:47389598 | C | T | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1583-1839C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389598 | |||||||
chr17:47389822 | A | G | 1 | a0005c0005t0001g0210 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1583-1615A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389822 | |||||||
chr17:47389940 | CTGTA | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-1492_1583-148 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389940 | ||||||
chr17:47389945 | T | A | 2 | a0003c0008t0001g0006 a0003c0008t0004g0005 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1583-1492T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389945 | |||||||
chr17:47390044 | A | G | 1 | a0002c0002t0001g0056 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1583-1393A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390044 | |||||||
chr17:47390116 | T | C | 334 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1583-1321T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390116 | |||||||
chr17:47390237 | T | C | 1 | a0002c0002t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1583-1200T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390237 | |||||||
chr17:47390238 | TGA | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-1193_1583-119 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390238 | ||||||
chr17:47390305 | C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-1132C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390305 | |||||||
chr17:47390325 | T | TAC | 10 | a0001c0001t0001g0120 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG00438.hp1 HG02165.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1583-1093_1583-109 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | ||||||
chr17:47390325 | T | TACACAC | 12 | a0003c0004t0002g0220 a0006c0007t0001g0059 a0006c0007t0001g0060 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1583-1097_1583-109 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | ||||||
chr17:47390325 | T | TACACACA others(3): Show |
34 | a0003c0004t0002g0216 a0003c0004t0002g0219 a0003c0004t0002g0222 others(31): Show |
35 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1583-1101_1583-109 others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | ||||||
chr17:47390325 | T | TACACACA others(5): Show |
1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-1103_1583-109 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | ||||||
chr17:47390325 | T | TACACACA others(7): Show |
40 | a0003c0004t0002g0109 a0003c0004t0002g0245 a0003c0008t0003g0276 others(37): Show |
43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1583-1105_1583-109 others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | ||||||
chr17:47390349 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1583-1088C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390349 | |||||||
chr17:47390910 | G | GTCTTATC others(6): Show |
1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-524_1583-523i others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390910 | ||||||
chr17:47390914 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-523G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390914 | |||||||
chr17:47390914 | G | GTCTA | 46 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0070 others(43): Show |
46 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1583-511_1583-508d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTATCT others(1): Show |
71 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(68): Show |
71 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1583-515_1583-508d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTATCT others(5): Show |
26 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0077 others(23): Show |
26 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1583-519_1583-508d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTATCT others(13): Show |
1 | a0001c0001t0001g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1583-508_1583-507i others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTA | 5 | a0003c0004t0002g0219 a0003c0004t0002g0234 a0003c0004t0002g0239 others(2): Show |
5 | HG02083.hp1 HG03688.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTATC others(2): Show |
29 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0220 others(26): Show |
30 | HG00558.hp1 HG01346.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(11): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTATC others(6): Show |
8 | a0003c0004t0002g0216 a0003c0004t0002g0228 a0003c0004t0002g0232 others(5): Show |
8 | HG00438.hp2 HG00544.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTATC others(10): Show |
3 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 |
3 | HG02647.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1583-520_1583-519i others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTATC others(14): Show |
4 | a0006c0007t0001g0060 a0006c0007t0001g0063 a0006c0007t0001g0064 others(1): Show |
4 | HG02135.hp2 NA18997.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390914 | G | GTCTTATC others(18): Show |
6 | a0006c0007t0001g0059 a0006c0007t0001g0062 a0006c0007t0001g0339 others(3): Show |
6 | HG00408.hp1 HG00423.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(27): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | ||||||
chr17:47390916 | C | CT | 35 | a0003c0004t0002g0245 a0004c0003t0001g0001 a0004c0003t0001g0003 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1583-520dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390916 | ||||||
chr17:47390930 | G | A | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1583-507G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390930 | |||||||
chr17:47391005 | T | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-432T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391005 | |||||||
chr17:47391026 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-411A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391026 | |||||||
chr17:47391054 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1583-383C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391054 | |||||||
chr17:47391216 | A | C | 1 | a0003c0004t0002g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1583-221A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391216 | |||||||
chr17:47391328 | G | A | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1583-109G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391328 | |||||||
chr17:47391591 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1726+11T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391591 | |||||||
chr17:47391641 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1726+61A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391641 | |||||||
chr17:47391665 | AT | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+92delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47391665 | ||||||
chr17:47391765 | C | T | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1726+185C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391765 | |||||||
chr17:47391787 | TA | T | 8 | a0001c0001t0001g0076 a0002c0002t0001g0263 a0002c0010t0001g0265 others(5): Show |
8 | HG00323.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1726+216delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47391787 | ||||||
chr17:47391788 | A | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+208A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391788 | |||||||
chr17:47391821 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+241A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391821 | |||||||
chr17:47391840 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1726+260T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391840 | |||||||
chr17:47391857 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+277G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391857 | |||||||
chr17:47391925 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1726+345A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391925 | |||||||
chr17:47392238 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1726+658G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392238 | |||||||
chr17:47392353 | C | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1726+773C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392353 | |||||||
chr17:47392487 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+907C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392487 | |||||||
chr17:47392879 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1727-1146A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392879 | |||||||
chr17:47392916 | T | G | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1727-1109T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392916 | |||||||
chr17:47392975 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-1050C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392975 | |||||||
chr17:47392992 | T | C | 49 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(46): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1727-1033T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392992 | |||||||
chr17:47392997 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-1028G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392997 | |||||||
chr17:47393072 | G | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1727-953G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393072 | |||||||
chr17:47393074 | G | A | 2 | a0003c0004t0002g0219 a0003c0004t0002g0239 |
2 | NA18747.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1727-951G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393074 | |||||||
chr17:47393091 | A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1727-934A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393091 | |||||||
chr17:47393101 | T | TA | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-914dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393101 | ||||||
chr17:47393177 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-848C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393177 | |||||||
chr17:47393334 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-691A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393334 | |||||||
chr17:47393357 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1727-668A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393357 | |||||||
chr17:47393409 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1727-616G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393409 | |||||||
chr17:47393412 | G | A | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1727-613G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393412 | |||||||
chr17:47393547 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-478A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393547 | |||||||
chr17:47393560 | A | C | 2 | a0002c0002t0001g0289 a0002c0002t0001g0295 |
2 | NA18987.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1727-465A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393560 | |||||||
chr17:47393717 | A | AAAAT | 44 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0262 others(41): Show |
44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1727-272_1727-269d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393717 | A | AAAATAAA others(1): Show |
22 | a0002c0010t0001g0267 a0002c0010t0001g0268 a0002c0010t0001g0269 others(19): Show |
22 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.1727-276_1727-269d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393717 | A | AAAATAAA others(5): Show |
1 | a0002c0010t0001g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1727-280_1727-269d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393717 | AAAAT | A | 144 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1727-272_1727-269d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393717 | AAAATAAA others(1): Show |
A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0001g0131 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1727-276_1727-269d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393717 | AAAATAAA others(5): Show |
A | 26 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0091 others(23): Show |
26 | HG00280.hp1 HG01071.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1727-280_1727-269d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | ||||||
chr17:47393753 | T | A | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1727-272T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393753 | |||||||
chr17:47393753 | TAAAA | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1727-270_1727-267d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393753 | ||||||
chr17:47393757 | A | T | 3 | a0002c0002t0008g0323 a0004c0003t0001g0033 a0005c0005t0001g0116 |
3 | HG01358.hp1 HG03669.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1727-268A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393757 | |||||||
chr17:47393766 | AAAT | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0128 |
3 | HG02132.hp2 NA19064.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1727-256_1727-254d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393766 | ||||||
chr17:47393862 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-163A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393862 | |||||||
chr17:47394339 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1801+240C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394339 | |||||||
chr17:47394618 | G | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1801+519G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394618 | |||||||
chr17:47394861 | CAG | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1801+765_1801+766d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr17 | 47394861 | ||||||
chr17:47394877 | A | G | 1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1801+778A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394877 | |||||||
chr17:47395030 | C | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1802-804C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395030 | |||||||
chr17:47395036 | C | T | 2 | a0002c0002t0001g0297 a0002c0002t0001g0300 |
2 | NA18991.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1802-798C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395036 | |||||||
chr17:47395037 | G | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1802-797G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395037 | |||||||
chr17:47395357 | T | G | 1 | a0002c0002t0008g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1802-477T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395357 | |||||||
chr17:47395435 | G | A | 1 | a0002c0002t0001g0291 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1802-399G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395435 | |||||||
chr17:47395741 | A | G | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1802-93A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395741 | |||||||
chr17:47395804 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1802-30C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395804 | |||||||
chr17:47396047 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945+70A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396047 | |||||||
chr17:47396258 | A | G | 5 | a0002c0002t0001g0259 a0002c0002t0001g0279 a0002c0002t0001g0294 others(2): Show |
5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+281A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396258 | |||||||
chr17:47396293 | G | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+316G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396293 | |||||||
chr17:47396664 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+687C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396664 | |||||||
chr17:47396748 | T | C | 3 | a0004c0003t0001g0027 a0004c0003t0001g0030 a0004c0003t0001g0040 |
3 | NA18956.hp1 NA18963.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1945+771T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396748 | |||||||
chr17:47396817 | G | A | 1 | a0003c0004t0002g0216 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1945+840G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396817 | |||||||
chr17:47396856 | T | C | 1 | a0004c0003t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1945+879T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396856 | |||||||
chr17:47397008 | GTCCCTC | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+1042_1945+104 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397008 | ||||||
chr17:47397019 | T | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1945+1042T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397019 | |||||||
chr17:47397027 | T | TCCC | 17 | a0003c0004t0002g0109 a0003c0004t0002g0219 a0003c0004t0002g0226 others(14): Show |
17 | HG00544.hp1 HG01515.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.1945+1053_1945+105 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397027 | ||||||
chr17:47397027 | T | TCCCC | 16 | a0003c0004t0002g0214 a0003c0004t0002g0216 a0003c0004t0002g0220 others(13): Show |
17 | HG00438.hp2 HG01346.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1945+1052_1945+105 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397027 | ||||||
chr17:47397033 | T | C | 1 | a0003c0004t0002g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1945+1056T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397033 | |||||||
chr17:47397033 | T | TC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0135 a0002c0002t0001g0319 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+1061dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397033 | ||||||
chr17:47397060 | G | C | 1 | a0004c0003t0001g0031 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1945+1083G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397060 | |||||||
chr17:47397157 | G | A | 139 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1945+1180G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397157 | |||||||
chr17:47397169 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1945+1192G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397169 | |||||||
chr17:47397201 | AC | A | 40 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1945+1225delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397201 | |||||||
chr17:47397202 | C | G | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1945+1225C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397202 | |||||||
chr17:47397242 | A | G | 2 | a0003c0004t0002g0222 a0003c0004t0002g0230 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1945+1265A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397242 | |||||||
chr17:47397353 | G | A | 1 | a0003c0004t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1945+1376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397353 | |||||||
chr17:47397410 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1945+1433T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397410 | |||||||
chr17:47397424 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945+1447C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397424 | |||||||
chr17:47397466 | GC | G | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1945+1491delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397466 | ||||||
chr17:47397489 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1512G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397489 | |||||||
chr17:47397540 | C | T | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+1563C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397540 | |||||||
chr17:47397542 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0126 |
2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1945+1565G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397542 | |||||||
chr17:47397552 | CATCTAGG others(33): Show |
C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1595_1945+163 others(44): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397552 | ||||||
chr17:47397555 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1945+1578C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397555 | |||||||
chr17:47397592 | T | C | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1945+1615T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397592 | |||||||
chr17:47397621 | G | A | 1 | a0004c0003t0001g0028 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945+1644G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397621 | |||||||
chr17:47397626 | C | G | 2 | a0003c0008t0001g0006 a0003c0008t0004g0005 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1945+1649C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397626 | |||||||
chr17:47397631 | C | A | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.1945+1654C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397631 | |||||||
chr17:47397664 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1687G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397664 | |||||||
chr17:47397669 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1945+1692G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397669 | |||||||
chr17:47397709 | A | T | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1945+1732A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397709 | |||||||
chr17:47397763 | A | ACCCTCCG others(32): Show |
3 | a0003c0004t0002g0222 a0003c0004t0002g0230 a0003c0004t0002g0233 |
3 | NA18942.hp1 NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1945+1796_1945+183 others(43): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397763 | ||||||
chr17:47397790 | A | C | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1945+1813A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397790 | |||||||
chr17:47397905 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+1928A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397905 | |||||||
chr17:47397937 | A | AGGCCAGC others(42): Show |
1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1967_1945+196 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397937 | ||||||
chr17:47397945 | C | CGCCCCGT others(43): Show |
1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1945+1995_1945+199 others(54): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397945 | ||||||
chr17:47397945 | C | CGCCCCGT others(42): Show |
81 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(78): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397945 | ||||||
chr17:47397945 | C | T | 2 | a0004c0003t0006g0260 a0016c0020t0001g0346 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1945+1968C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397945 | |||||||
chr17:47397946 | G | GCCCCGTC others(42): Show |
4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397946 | ||||||
chr17:47397951 | G | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+1974G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397951 | |||||||
chr17:47397965 | T | TGGGGGGG others(43): Show |
3 | a0003c0004t0001g0141 a0003c0004t0002g0234 a0004c0003t0001g0067 |
3 | HG02965.hp1 NA18985.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(54): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397965 | ||||||
chr17:47398000 | G | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2023G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398000 | |||||||
chr17:47398013 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1945+2036G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398013 | |||||||
chr17:47398020 | G | A | 2 | a0003c0008t0004g0157 a0003c0008t0004g0258 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1945+2043G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398020 | |||||||
chr17:47398020 | G | C | 41 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1945+2043G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398020 | |||||||
chr17:47398030 | TGCCCGGC others(42): Show |
T | 14 | a0002c0002t0001g0010 a0002c0002t0001g0262 a0002c0002t0001g0263 others(11): Show |
14 | HG02615.hp1 HG02717.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945+2068_1945+211 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398030 | ||||||
chr17:47398035 | G | A | 37 | a0002c0002t0001g0291 a0004c0003t0001g0001 a0004c0003t0001g0003 others(34): Show |
40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1945+2058G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398035 | |||||||
chr17:47398043 | G | A | 13 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1945+2066G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398043 | |||||||
chr17:47398045 | T | C | 2 | a0006c0007t0001g0059 a0006c0007t0001g0062 |
2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1945+2068T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398045 | |||||||
chr17:47398051 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1945+2074C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398051 | |||||||
chr17:47398065 | G | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2088G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398065 | |||||||
chr17:47398079 | CGCCCGGC others(119): Show |
C | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1945+2152_1945+227 others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398079 | ||||||
chr17:47398097 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1945+2120G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398097 | |||||||
chr17:47398101 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1945+2124G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398101 | |||||||
chr17:47398127 | C | G | 5 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 others(2): Show |
5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+2150C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398127 | |||||||
chr17:47398128 | C | CG | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1945+2151_1945+215 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398128 | |||||||
chr17:47398130 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1945+2153C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398130 | |||||||
chr17:47398130 | CT | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0152 a0001c0001t0001g0166 |
3 | HG02135.hp1 HG02257.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1945+2154delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398130 | |||||||
chr17:47398173 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2196A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398173 | |||||||
chr17:47398173 | AGCCGCCC others(120): Show |
A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0309 |
2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1945+2238_1945+236 others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398173 | ||||||
chr17:47398226 | C | T | 14 | a0001c0001t0001g0019 a0006c0007t0001g0059 a0006c0007t0001g0060 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945+2249C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398226 | |||||||
chr17:47398258 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2281C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398258 | |||||||
chr17:47398259 | G | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+2282G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398259 | |||||||
chr17:47398267 | A | G | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398267 | |||||||
chr17:47398273 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2296C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398273 | |||||||
chr17:47398276 | G | A | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1945+2299G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398276 | |||||||
chr17:47398303 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2326C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398303 | |||||||
chr17:47398401 | C | T | 1 | a0003c0008t0004g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1945+2424C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398401 | |||||||
chr17:47398421 | G | C | 1 | a0007c0009t0002g0235 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1945+2444G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398421 | |||||||
chr17:47398432 | G | A | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1945+2455G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398432 | |||||||
chr17:47398466 | T | G | 1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1945+2489T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398466 | |||||||
chr17:47398469 | G | C | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.1945+2492G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398469 | |||||||
chr17:47398474 | G | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1945+2497G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398474 | |||||||
chr17:47398480 | G | A | 1 | a0003c0004t0002g0245 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1945+2503G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398480 | |||||||
chr17:47398577 | T | A | 1 | a0004c0003t0001g0028 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945+2600T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398577 | |||||||
chr17:47398783 | G | C | 237 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1945+2806G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398783 | |||||||
chr17:47398824 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2847C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398824 | |||||||
chr17:47398850 | AAAAT | A | 40 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(37): Show |
43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1945+2893_1945+289 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398850 | ||||||
chr17:47398906 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2929A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398906 | |||||||
chr17:47398930 | C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2953C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398930 | |||||||
chr17:47398934 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1945+2957C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398934 | |||||||
chr17:47398984 | C | T | 1 | a0004c0003t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1945+3007C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398984 | |||||||
chr17:47398993 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1945+3016G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398993 | |||||||
chr17:47399020 | T | A | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+3043T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399020 | |||||||
chr17:47399075 | A | G | 1 | a0004c0003t0001g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1946-3057A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399075 | |||||||
chr17:47399277 | T | C | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1946-2855T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399277 | |||||||
chr17:47399293 | CAT | C | 3 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG03654.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1946-2838_1946-283 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399293 | |||||||
chr17:47399367 | A | G | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1946-2765A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399367 | |||||||
chr17:47399670 | C | T | 1 | a0001c0001t0005g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1946-2462C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399670 | |||||||
chr17:47399680 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1946-2452C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399680 | |||||||
chr17:47399714 | G | GTGGTA | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1946-2416_1946-241 others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47399714 | ||||||
chr17:47399732 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1946-2400T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399732 | |||||||
chr17:47399793 | G | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1946-2339G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399793 | |||||||
chr17:47399806 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1946-2326G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399806 | |||||||
chr17:47399853 | T | C | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1946-2279T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399853 | |||||||
chr17:47399859 | C | T | 91 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1946-2273C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399859 | |||||||
chr17:47399922 | C | CA | 3 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0146 |
3 | NA18993.hp1 NA19009.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1946-2205dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47399922 | ||||||
chr17:47399929 | G | A | 3 | a0004c0003t0001g0027 a0004c0003t0001g0030 a0004c0003t0001g0040 |
3 | NA18956.hp1 NA18963.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1946-2203G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399929 | |||||||
chr17:47399977 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1946-2155C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399977 | |||||||
chr17:47400003 | A | G | 1 | a0005c0005t0001g0202 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1946-2129A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400003 | |||||||
chr17:47400207 | C | T | 236 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(233): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1946-1925C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400207 | |||||||
chr17:47400260 | A | G | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1946-1872A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400260 | |||||||
chr17:47400302 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1946-1830G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400302 | |||||||
chr17:47400455 | C | T | 1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1946-1677C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400455 | |||||||
chr17:47400598 | CTTGCCTC others(1): Show |
C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0150 a0008c0011t0001g0054 others(1): Show |
4 | HG01891.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1946-1533_1946-152 others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400598 | |||||||
chr17:47400814 | G | T | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1946-1318G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400814 | |||||||
chr17:47400815 | C | T | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1946-1317C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400815 | |||||||
chr17:47401092 | G | A | 1 | a0004c0003t0001g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1946-1040G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401092 | |||||||
chr17:47401116 | A | AT | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1946-1016_1946-101 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401116 | |||||||
chr17:47401217 | A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-915A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401217 | |||||||
chr17:47401372 | C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-760C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401372 | |||||||
chr17:47401477 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1946-655A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401477 | |||||||
chr17:47401590 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-542A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401590 | |||||||
chr17:47401597 | A | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1946-535A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401597 | |||||||
chr17:47401640 | C | CT | 118 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(115): Show |
118 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1946-470dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | ||||||
chr17:47401640 | C | CTT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0088 others(3): Show |
6 | HG02027.hp1 HG02055.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1946-471_1946-470d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | ||||||
chr17:47401640 | CT | C | 57 | a0002c0002t0001g0286 a0002c0002t0001g0322 a0002c0002t0003g0336 others(54): Show |
60 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1946-470delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | ||||||
chr17:47401643 | T | C | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1946-489T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401643 | |||||||
chr17:47401669 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1946-463G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401669 | |||||||
chr17:47401733 | C | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1946-399C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401733 | |||||||
chr17:47401930 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1946-202C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401930 | |||||||
chr17:47402080 | A | C | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.1946-52A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47402080 | |||||||
chr17:47402321 | T | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017+118T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402321 | |||||||
chr17:47402330 | G | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2017+127G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402330 | |||||||
chr17:47402340 | C | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2017+137C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402340 | |||||||
chr17:47402367 | A | C | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2017+164A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402367 | |||||||
chr17:47402473 | G | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2017+270G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402473 | |||||||
chr17:47402551 | C | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2017+348C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402551 | |||||||
chr17:47402801 | T | A | 11 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(8): Show |
11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2017+598T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402801 | |||||||
chr17:47402963 | G | C | 1 | a0008c0011t0001g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2017+760G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402963 | |||||||
chr17:47403162 | T | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-716T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403162 | |||||||
chr17:47403245 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-633G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403245 | |||||||
chr17:47403392 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2018-486A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403392 | |||||||
chr17:47403527 | G | A | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2018-351G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403527 | |||||||
chr17:47403691 | C | T | 96 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(93): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2018-187C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403691 | |||||||
chr17:47403825 | G | A | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2018-53G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403825 | |||||||
chr17:47403835 | A | G | 1 | a0003c0016t0002g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2018-43A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403835 | |||||||
chr17:47404048 | GT | G | 7 | a0003c0004t0002g0222 a0003c0004t0002g0230 a0003c0004t0002g0233 others(4): Show |
7 | NA18942.hp1 NA18946.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2161+37delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr17 | 47404048 | ||||||
chr17:47404199 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2161+178T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404199 | |||||||
chr17:47404265 | T | G | 1 | a0006c0007t0010g0061 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2161+244T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404265 | |||||||
chr17:47404497 | T | C | 2 | a0001c0013t0001g0196 a0001c0013t0001g0197 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2162-65T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404497 | |||||||
chr17:47405180 | G | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2233+547G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405180 | |||||||
chr17:47405446 | T | A | 89 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(86): Show |
93 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2233+813T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405446 | |||||||
chr17:47405491 | A | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2233+858A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405491 | |||||||
chr17:47405525 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2233+892T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405525 | |||||||
chr17:47405549 | T | C | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2233+916T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405549 | |||||||
chr17:47405709 | G | T | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+1076G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405709 | |||||||
chr17:47405807 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2233+1174T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405807 | |||||||
chr17:47405863 | A | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2233+1230A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405863 | |||||||
chr17:47405913 | AT | A | 44 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(41): Show |
44 | HG00673.hp2 HG01070.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2233+1288delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47405913 | ||||||
chr17:47406074 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2233+1441T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406074 | |||||||
chr17:47406129 | T | C | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2233+1496T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406129 | |||||||
chr17:47406136 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2233+1503G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406136 | |||||||
chr17:47406256 | T | C | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+1623T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406256 | |||||||
chr17:47406503 | G | A | 1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2233+1870G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406503 | |||||||
chr17:47406582 | A | G | 1 | a0002c0002t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2233+1949A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406582 | |||||||
chr17:47406633 | T | G | 3 | a0003c0004t0002g0237 a0003c0004t0002g0250 a0013c0017t0001g0209 |
3 | HG02056.hp2 NA18943.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2233+2000T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406633 | |||||||
chr17:47406683 | G | A | 3 | a0006c0007t0001g0339 a0006c0007t0001g0340 a0006c0007t0001g0341 |
3 | HG00423.hp2 NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2233+2050G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406683 | |||||||
chr17:47406745 | G | A | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+2112G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406745 | |||||||
chr17:47407064 | TA | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2233+2435delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47407064 | ||||||
chr17:47407121 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2233+2488T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407121 | |||||||
chr17:47407174 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2234-2473G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407174 | |||||||
chr17:47407214 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2234-2433T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407214 | |||||||
chr17:47407573 | T | C | 1 | a0017c0026t0001g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2234-2074T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407573 | |||||||
chr17:47407680 | A | G | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2234-1967A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407680 | |||||||
chr17:47407744 | TTTTGTTT others(4): Show |
T | 1 | a0001c0001t0001g0136 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2234-1888_2234-187 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47407744 | ||||||
chr17:47407819 | T | C | 1 | a0002c0002t0001g0291 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2234-1828T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407819 | |||||||
chr17:47407821 | A | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2234-1826A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407821 | |||||||
chr17:47408373 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2234-1274G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408373 | |||||||
chr17:47408410 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
19 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2234-1237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408410 | |||||||
chr17:47408504 | T | C | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2234-1143T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408504 | |||||||
chr17:47408616 | C | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.2234-1031C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408616 | |||||||
chr17:47408631 | G | A | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2234-1016G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408631 | |||||||
chr17:47408637 | A | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2234-1010A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408637 | |||||||
chr17:47408654 | G | A | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2234-993G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408654 | |||||||
chr17:47408975 | T | G | 1 | a0004c0003t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2234-672T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408975 | |||||||
chr17:47409111 | A | G | 6 | a0007c0009t0001g0221 a0007c0009t0002g0218 a0007c0009t0002g0235 others(3): Show |
6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2234-536A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409111 | |||||||
chr17:47409234 | A | G | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2234-413A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409234 | |||||||
chr17:47409285 | T | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2234-362T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409285 | |||||||
chr17:47409303 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2234-344C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409303 | |||||||
chr17:47409396 | G | A | 1 | a0002c0010t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2234-251G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409396 | |||||||
chr17:47409450 | CCAAGTA | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2234-196_2234-191d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409450 | |||||||
chr17:47409483 | A | G | 1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2234-164A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409483 | |||||||
chr17:47409765 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2278+74A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47409765 | |||||||
chr17:47410069 | G | A | 96 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(93): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2278+378G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410069 | |||||||
chr17:47410118 | T | TA | 91 | a0001c0001t0005g0255 a0002c0002t0001g0294 a0003c0004t0001g0141 others(88): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2278+439dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr17 | 47410118 | ||||||
chr17:47410254 | G | A | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2278+563G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410254 | |||||||
chr17:47410705 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0145 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2278+1014A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410705 | |||||||
chr17:47410800 | G | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2278+1109G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410800 | |||||||
chr17:47410843 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2278+1152C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410843 | |||||||
chr17:47411037 | A | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2278+1346A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411037 | |||||||
chr17:47411041 | T | C | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2278+1350T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411041 | |||||||
chr17:47411240 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0176 |
2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2279-1533C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411240 | |||||||
chr17:47411369 | C | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2279-1404C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411369 | |||||||
chr17:47411510 | G | T | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2279-1263G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411510 | |||||||
chr17:47411515 | A | G | 49 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(46): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.2279-1258A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411515 | |||||||
chr17:47411556 | T | G | 1 | a0003c0004t0002g0237 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2279-1217T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411556 | |||||||
chr17:47411940 | A | T | 5 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 others(2): Show |
5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2279-833A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411940 | |||||||
chr17:47412279 | T | G | 1 | a0003c0004t0002g0216 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2279-494T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412279 | |||||||
chr17:47412392 | T | C | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2279-381T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412392 | |||||||
chr17:47412413 | C | G | 2 | a0001c0013t0001g0196 a0001c0013t0001g0197 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2279-360C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412413 | |||||||
chr17:47412593 | G | T | 2 | a0005c0005t0001g0110 a0005c0005t0001g0116 |
2 | NA19000.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2279-180G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412593 | |||||||
chr17:47413010 | G | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2422+94G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413010 | |||||||
chr17:47413153 | A | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2422+237A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413153 | |||||||
chr17:47413245 | AT | A | 232 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(229): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2422+339delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47413245 | ||||||
chr17:47413310 | A | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2422+394A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413310 | |||||||
chr17:47413642 | T | C | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2422+726T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413642 | |||||||
chr17:47413731 | A | AT | 53 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(50): Show |
56 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2422+825dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47413731 | ||||||
chr17:47414239 | A | ATG | 235 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(232): Show |
239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2423-598_2423-597d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414239 | ||||||
chr17:47414253 | A | G | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2423-595A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414253 | |||||||
chr17:47414426 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2423-422C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414426 | |||||||
chr17:47414512 | C | CA | 8 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0003c0008t0004g0005 others(5): Show |
8 | HG01106.hp1 HG02809.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.2423-319dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414512 | ||||||
chr17:47414512 | CA | C | 93 | a0001c0001t0001g0087 a0001c0001t0001g0136 a0001c0001t0001g0161 others(90): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2423-319delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414512 | ||||||
chr17:47414570 | C | T | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2423-278C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414570 | |||||||
chr17:47414613 | C | T | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2423-235C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414613 | |||||||
chr17:47414692 | A | C | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2423-156A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414692 | |||||||
chr17:47414935 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+16T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414935 | |||||||
chr17:47414965 | T | C | 2 | a0002c0002t0001g0334 a0014c0018t0001g0337 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2494+46T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414965 | |||||||
chr17:47414975 | A | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+56A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414975 | |||||||
chr17:47415137 | A | C | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2494+218A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415137 | |||||||
chr17:47415138 | C | A | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2494+219C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415138 | |||||||
chr17:47415158 | A | G | 1 | a0004c0003t0001g0035 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2494+239A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415158 | |||||||
chr17:47415276 | T | C | 1 | a0003c0004t0002g0237 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2494+357T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415276 | |||||||
chr17:47415314 | C | G | 1 | a0003c0004t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2494+395C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415314 | |||||||
chr17:47415368 | C | A | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2494+449C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415368 | |||||||
chr17:47415634 | CAT | C | 3 | a0006c0007t0001g0339 a0006c0007t0001g0340 a0006c0007t0001g0341 |
3 | HG00423.hp2 NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2494+716_2494+717d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415634 | |||||||
chr17:47415890 | G | A | 2 | a0008c0011t0001g0054 a0008c0011t0001g0273 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2494+971G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415890 | |||||||
chr17:47415965 | A | AT | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+1046_2494+104 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415965 | |||||||
chr17:47415966 | C | T | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+1047C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415966 | |||||||
chr17:47415984 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2494+1065A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415984 | |||||||
chr17:47415997 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2494+1078C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415997 | |||||||
chr17:47416065 | T | C | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2494+1146T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416065 | |||||||
chr17:47416328 | G | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+1409G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416328 | |||||||
chr17:47416460 | T | C | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2494+1541T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416460 | |||||||
chr17:47416485 | C | T | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+1566C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416485 | |||||||
chr17:47416648 | G | A | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2494+1729G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416648 | |||||||
chr17:47416751 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+1832C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416751 | |||||||
chr17:47417224 | G | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+2305G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417224 | |||||||
chr17:47417279 | G | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2494+2360G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417279 | |||||||
chr17:47417473 | C | A | 1 | a0002c0010t0001g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2494+2554C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417473 | |||||||
chr17:47417498 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+2579C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417498 | |||||||
chr17:47417543 | C | T | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+2624C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417543 | |||||||
chr17:47417904 | G | A | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2494+2985G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417904 | |||||||
chr17:47418238 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+3319C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418238 | |||||||
chr17:47418319 | A | G | 5 | a0002c0002t0001g0259 a0002c0002t0001g0279 a0002c0002t0001g0294 others(2): Show |
5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494+3400A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418319 | |||||||
chr17:47418340 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+3421T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418340 | |||||||
chr17:47418374 | C | CG | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+3455_2494+345 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418374 | |||||||
chr17:47418401 | A | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+3482A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418401 | |||||||
chr17:47418511 | A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2494+3592A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418511 | |||||||
chr17:47419014 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2494+4095G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419014 | |||||||
chr17:47419250 | A | G | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+4331A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419250 | |||||||
chr17:47419302 | T | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+4383T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419302 | |||||||
chr17:47419330 | A | G | 3 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 |
3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2494+4411A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419330 | |||||||
chr17:47419508 | T | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+4589T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419508 | |||||||
chr17:47419726 | G | A | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+4807G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419726 | |||||||
chr17:47419767 | C | T | 1 | a0004c0003t0006g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2494+4848C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419767 | |||||||
chr17:47419829 | T | C | 1 | a0001c0001t0005g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2494+4910T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419829 | |||||||
chr17:47419867 | A | T | 2 | a0002c0002t0001g0089 a0003c0004t0001g0141 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2494+4948A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419867 | |||||||
chr17:47419913 | C | CCCCTCT | 133 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
133 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2494+5018_2494+502 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47419913 | ||||||
chr17:47419913 | CCCCTCT | C | 5 | a0001c0001t0001g0137 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | NA18962.hp2 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+5018_2494+502 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47419913 | ||||||
chr17:47419961 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2494+5042C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419961 | |||||||
chr17:47419969 | C | G | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+5050C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419969 | |||||||
chr17:47419978 | C | A | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+5059C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419978 | |||||||
chr17:47419993 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+5074G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419993 | |||||||
chr17:47420000 | G | A | 29 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0091 others(26): Show |
29 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2494+5081G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420000 | |||||||
chr17:47420010 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5091C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420010 | |||||||
chr17:47420052 | A | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+5133A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420052 | |||||||
chr17:47420073 | A | G | 234 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2494+5154A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420073 | |||||||
chr17:47420182 | T | C | 234 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2494+5263T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420182 | |||||||
chr17:47420209 | A | G | 49 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(46): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.2494+5290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420209 | |||||||
chr17:47420215 | C | G | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2494+5296C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420215 | |||||||
chr17:47420240 | C | T | 1 | a0006c0007t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2494+5321C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420240 | |||||||
chr17:47420340 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5421C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420340 | |||||||
chr17:47420341 | G | A | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2494+5422G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420341 | |||||||
chr17:47420555 | C | T | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+5636C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420555 | |||||||
chr17:47420635 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+5716C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420635 | |||||||
chr17:47420639 | A | G | 2 | a0002c0002t0001g0262 a0002c0002t0001g0266 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2494+5720A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420639 | |||||||
chr17:47420662 | G | A | 1 | a0002c0002t0001g0334 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2494+5743G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420662 | |||||||
chr17:47420671 | C | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5752C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420671 | |||||||
chr17:47420681 | G | A | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+5762G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420681 | |||||||
chr17:47420698 | A | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+5779A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420698 | |||||||
chr17:47420698 | ACCCTCCG others(33): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2494+5797_2494+583 others(44): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47420698 | ||||||
chr17:47420704 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5785C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420704 | |||||||
chr17:47420708 | C | T | 1 | a0005c0005t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2494+5789C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420708 | |||||||
chr17:47420721 | A | G | 231 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(228): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2494+5802A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420721 | |||||||
chr17:47420740 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5821C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420740 | |||||||
chr17:47420749 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+5830G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420749 | |||||||
chr17:47420793 | G | A | 5 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0334 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+5874G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420793 | |||||||
chr17:47420825 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | HG01433.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2494+5906C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420825 | |||||||
chr17:47420829 | C | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+5910C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420829 | |||||||
chr17:47420860 | G | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.2494+5941G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420860 | |||||||
chr17:47420868 | G | T | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+5949G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420868 | |||||||
chr17:47420878 | C | T | 17 | a0001c0006t0003g0096 a0001c0006t0003g0101 a0002c0002t0001g0325 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2494+5959C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420878 | |||||||
chr17:47420879 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+5960G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420879 | |||||||
chr17:47420891 | G | A | 4 | a0008c0011t0001g0049 a0008c0011t0001g0050 a0008c0011t0001g0054 others(1): Show |
4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+5972G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420891 | |||||||
chr17:47420913 | C | A | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+5994C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420913 | |||||||
chr17:47420927 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+6008C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420927 | |||||||
chr17:47420967 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2494+6048C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420967 | |||||||
chr17:47420994 | G | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6075G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420994 | |||||||
chr17:47421006 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6087G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421006 | |||||||
chr17:47421009 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494+6090C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421009 | |||||||
chr17:47421010 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6091G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421010 | |||||||
chr17:47421020 | T | TG | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2494+6108dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421020 | ||||||
chr17:47421042 | G | C | 3 | a0002c0002t0001g0307 a0002c0002t0001g0314 a0002c0002t0009g0313 |
3 | NA18961.hp1 NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2494+6123G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421042 | |||||||
chr17:47421083 | G | A | 1 | a0002c0002t0001g0316 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2494+6164G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421083 | |||||||
chr17:47421086 | C | T | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2494+6167C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421086 | |||||||
chr17:47421119 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2494+6200C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421119 | |||||||
chr17:47421132 | G | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2494+6213G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421132 | |||||||
chr17:47421234 | C | G | 1 | a0008c0011t0001g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2494+6315C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421234 | |||||||
chr17:47421255 | T | G | 11 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(8): Show |
11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2494+6336T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421255 | |||||||
chr17:47421358 | CAT | C | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6440_2494+644 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421358 | |||||||
chr17:47421364 | T | C | 90 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(87): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+6445T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421364 | |||||||
chr17:47421562 | T | C | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+6643T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421562 | |||||||
chr17:47421571 | G | T | 130 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.2494+6652G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421571 | |||||||
chr17:47421582 | G | C | 96 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(93): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2494+6663G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421582 | |||||||
chr17:47421600 | C | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6681C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421600 | |||||||
chr17:47421600 | C | T | 1 | a0003c0008t0003g0276 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2494+6681C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421600 | |||||||
chr17:47421624 | T | TAAA | 183 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(180): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.2494+6711_2494+671 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421624 | ||||||
chr17:47421629 | A | AAAAAAAT | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6713_2494+671 others(11): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421629 | ||||||
chr17:47421633 | G | A | 35 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2494+6714G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421633 | |||||||
chr17:47421633 | G | T | 41 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2494+6714G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421633 | |||||||
chr17:47421637 | G | T | 36 | a0003c0004t0001g0141 a0004c0003t0001g0001 a0004c0003t0001g0003 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+6718G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421637 | |||||||
chr17:47421640 | AG | A | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6722delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421640 | |||||||
chr17:47421641 | G | GAA | 160 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(157): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.2494+6733_2494+673 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421641 | ||||||
chr17:47421641 | G | GAAAGAA | 35 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(32): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2494+6725_2494+672 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421641 | ||||||
chr17:47421653 | AG | A | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+6735delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421653 | |||||||
chr17:47421654 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+6735G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421654 | |||||||
chr17:47421869 | A | T | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2494+6950A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421869 | |||||||
chr17:47421945 | T | C | 1 | a0001c0022t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2494+7026T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421945 | |||||||
chr17:47422030 | A | G | 2 | a0002c0002t0001g0262 a0002c0002t0001g0266 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2494+7111A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422030 | |||||||
chr17:47422038 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2494+7119T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422038 | |||||||
chr17:47422055 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2494+7136A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422055 | |||||||
chr17:47422091 | G | T | 5 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0334 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+7172G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422091 | |||||||
chr17:47422138 | TATTA | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+7225_2494+722 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47422138 | ||||||
chr17:47422145 | TAAC | T | 13 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+7229_2494+723 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47422145 | ||||||
chr17:47422165 | C | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2494+7246C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422165 | |||||||
chr17:47422723 | C | A | 1 | a0002c0010t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2495-7095C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422723 | |||||||
chr17:47422742 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-7076A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422742 | |||||||
chr17:47422917 | C | T | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2495-6901C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422917 | |||||||
chr17:47423249 | G | T | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-6569G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423249 | |||||||
chr17:47423261 | T | A | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2495-6557T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423261 | |||||||
chr17:47423312 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2495-6506G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423312 | |||||||
chr17:47423400 | A | T | 1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2495-6418A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423400 | |||||||
chr17:47423411 | G | T | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2495-6407G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423411 | |||||||
chr17:47423481 | C | A | 1 | a0015c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2495-6337C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423481 | |||||||
chr17:47423495 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-6323C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423495 | |||||||
chr17:47423533 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2495-6285C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423533 | |||||||
chr17:47423607 | CCGCGCGC others(47): Show |
C | 1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2495-6204_2495-615 others(58): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47423607 | ||||||
chr17:47423802 | C | CACCCTCC others(8): Show |
3 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 |
3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2495-6005_2495-599 others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47423802 | ||||||
chr17:47424210 | C | T | 1 | a0002c0002t0001g0333 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2495-5608C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424210 | |||||||
chr17:47424443 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2495-5375A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424443 | |||||||
chr17:47424502 | A | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0317 |
2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.2495-5316A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424502 | |||||||
chr17:47424601 | T | A | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2495-5217T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424601 | |||||||
chr17:47424659 | CA | C | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2495-5158delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424659 | |||||||
chr17:47424730 | G | C | 234 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2495-5088G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424730 | |||||||
chr17:47424799 | A | G | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2495-5019A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424799 | |||||||
chr17:47424874 | C | CT | 58 | a0001c0013t0001g0196 a0001c0013t0001g0197 a0002c0002t0001g0056 others(55): Show |
61 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2495-4918dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTT | 8 | a0001c0001t0001g0169 a0002c0002t0001g0301 a0002c0002t0001g0310 others(5): Show |
8 | HG01106.hp2 HG02015.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-4919_2495-491 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0203 a0001c0006t0002g0099 others(1): Show |
4 | HG01175.hp1 HG02683.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-4928_2495-491 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0070 a0001c0001t0001g0185 a0001c0001t0001g0186 others(8): Show |
11 | HG00280.hp1 HG01517.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2495-4929_2495-491 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(6): Show |
14 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0189 others(11): Show |
14 | HG01192.hp1 HG01256.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-4930_2495-491 others(17): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(7): Show |
32 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0113 others(29): Show |
32 | HG01070.hp2 HG01074.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.2495-4931_2495-491 others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(8): Show |
24 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0114 others(21): Show |
24 | HG00423.hp2 HG01081.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.2495-4932_2495-491 others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(9): Show |
19 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0081 others(16): Show |
19 | HG00408.hp1 HG01106.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.2495-4933_2495-491 others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0111 others(10): Show |
13 | HG00673.hp2 HG01243.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.2495-4934_2495-491 others(21): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0104 others(5): Show |
8 | HG00323.hp1 HG00408.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4935_2495-491 others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(12): Show |
11 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0122 others(8): Show |
11 | HG02109.hp2 HG02602.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.2495-4936_2495-491 others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(13): Show |
10 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0080 others(7): Show |
10 | HG00741.hp1 HG01074.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-4937_2495-491 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(14): Show |
8 | a0001c0001t0001g0086 a0001c0001t0001g0145 a0001c0006t0001g0098 others(5): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4938_2495-491 others(25): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(15): Show |
9 | a0001c0001t0001g0051 a0001c0006t0001g0097 a0001c0006t0001g0100 others(6): Show |
9 | HG00438.hp1 HG00735.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-4939_2495-491 others(26): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0131 a0001c0001t0001g0150 a0001c0006t0001g0093 others(5): Show |
8 | HG01168.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4940_2495-491 others(27): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(17): Show |
2 | a0002c0002t0001g0089 a0002c0002t0003g0284 |
2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2495-4941_2495-491 others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0154 a0001c0006t0002g0092 a0001c0006t0003g0096 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-4942_2495-491 others(29): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(19): Show |
2 | a0005c0005t0001g0071 a0005c0005t0003g0327 |
2 | HG00423.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2495-4943_2495-491 others(30): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | C | CTTTTTTT others(22): Show |
3 | a0001c0006t0003g0101 a0003c0008t0004g0157 a0003c0008t0004g0258 |
3 | HG02818.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2495-4918_2495-491 others(33): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | CT | C | 7 | a0002c0002t0003g0057 a0003c0004t0002g0109 a0003c0004t0002g0239 others(4): Show |
7 | HG01255.hp1 HG03471.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-4918delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | CTT | C | 39 | a0001c0006t0001g0095 a0002c0002t0003g0055 a0002c0002t0003g0058 others(36): Show |
40 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2495-4919_2495-491 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424874 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-4928_2495-491 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | ||||||
chr17:47424896 | T | TTTTTTTT others(13): Show |
1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2495-4918_2495-491 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424896 | ||||||
chr17:47424964 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG01169.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2495-4854G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424964 | |||||||
chr17:47424976 | G | C | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2495-4842G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424976 | |||||||
chr17:47424977 | G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-4841G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424977 | |||||||
chr17:47425007 | C | T | 11 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(8): Show |
11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2495-4811C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425007 | |||||||
chr17:47425099 | G | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-4719G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425099 | |||||||
chr17:47425125 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-4693G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425125 | |||||||
chr17:47425171 | C | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0198 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4647C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425171 | |||||||
chr17:47425210 | A | C | 1 | a0005c0005t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2495-4608A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425210 | |||||||
chr17:47425442 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2495-4376T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425442 | |||||||
chr17:47425473 | T | G | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2495-4345T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425473 | |||||||
chr17:47425650 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2495-4168G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425650 | |||||||
chr17:47425662 | T | C | 1 | a0017c0026t0001g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2495-4156T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425662 | |||||||
chr17:47425755 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0189 |
2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2495-4063T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425755 | |||||||
chr17:47425859 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2495-3959A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425859 | |||||||
chr17:47425887 | G | C | 1 | a0002c0002t0003g0331 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2495-3931G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425887 | |||||||
chr17:47425891 | C | T | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2495-3927C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425891 | |||||||
chr17:47425980 | A | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3838A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425980 | |||||||
chr17:47426173 | T | C | 41 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(38): Show |
44 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2495-3645T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426173 | |||||||
chr17:47426252 | T | C | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3566T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426252 | |||||||
chr17:47426387 | T | C | 3 | a0001c0015t0001g0106 a0001c0015t0001g0192 a0001c0024t0001g0191 |
3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2495-3431T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426387 | |||||||
chr17:47426555 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-3263T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426555 | |||||||
chr17:47426658 | T | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2495-3160T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426658 | |||||||
chr17:47426907 | T | C | 1 | a0002c0002t0003g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2495-2911T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426907 | |||||||
chr17:47427005 | T | G | 1 | a0003c0004t0002g0234 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2495-2813T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427005 | |||||||
chr17:47427201 | A | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-2617A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427201 | |||||||
chr17:47427320 | A | G | 1 | a0004c0003t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2495-2498A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427320 | |||||||
chr17:47427504 | C | T | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-2314C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427504 | |||||||
chr17:47427786 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2495-2032C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427786 | |||||||
chr17:47427816 | T | C | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2495-2002T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427816 | |||||||
chr17:47427828 | T | C | 7 | a0002c0002t0001g0010 a0002c0002t0001g0262 a0002c0002t0001g0266 others(4): Show |
7 | HG02895.hp2 HG02922.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-1990T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427828 | |||||||
chr17:47427913 | T | A | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-1905T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427913 | |||||||
chr17:47427988 | C | A | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2495-1830C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427988 | |||||||
chr17:47428086 | T | C | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2495-1732T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428086 | |||||||
chr17:47428127 | CTA | C | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-1689_2495-168 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47428127 | ||||||
chr17:47428323 | T | TC | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-1494dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47428323 | ||||||
chr17:47428488 | A | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0300 |
2 | NA18991.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2495-1330A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428488 | |||||||
chr17:47428490 | G | A | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-1328G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428490 | |||||||
chr17:47428545 | A | G | 1 | a0002c0002t0001g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2495-1273A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428545 | |||||||
chr17:47428835 | T | C | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2495-983T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428835 | |||||||
chr17:47429238 | T | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-580T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429238 | |||||||
chr17:47429247 | C | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2495-571C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429247 | |||||||
chr17:47429316 | T | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2495-502T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429316 | |||||||
chr17:47429464 | T | C | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-354T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429464 | |||||||
chr17:47429546 | A | AG | 40 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(37): Show |
43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2495-269dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47429546 | ||||||
chr17:47429564 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-254C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429564 | |||||||
chr17:47430002 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2638+41C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430002 | |||||||
chr17:47430091 | G | A | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2638+130G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430091 | |||||||
chr17:47430131 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2638+170G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430131 | |||||||
chr17:47430185 | A | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2638+224A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430185 | |||||||
chr17:47430220 | T | G | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+259T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430220 | |||||||
chr17:47430850 | T | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+889T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430850 | |||||||
chr17:47430928 | A | C | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+967A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430928 | |||||||
chr17:47430948 | G | A | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+987G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430948 | |||||||
chr17:47431325 | C | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2638+1364C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431325 | |||||||
chr17:47431524 | T | C | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+1563T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431524 | |||||||
chr17:47431605 | T | C | 1 | a0005c0005t0002g0225 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2638+1644T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431605 | |||||||
chr17:47431676 | T | C | 5 | a0004c0003t0001g0003 a0004c0003t0001g0020 a0004c0003t0001g0021 others(2): Show |
6 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.2638+1715T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431676 | |||||||
chr17:47431744 | T | G | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2638+1783T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431744 | |||||||
chr17:47432088 | T | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2638+2127T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432088 | |||||||
chr17:47432130 | G | A | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.2638+2169G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432130 | |||||||
chr17:47432130 | G | C | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2638+2169G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432130 | |||||||
chr17:47432181 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2638+2220C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432181 | |||||||
chr17:47432328 | G | C | 8 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0198 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2638+2367G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432328 | |||||||
chr17:47432399 | A | AAAAT | 80 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(77): Show |
intron_variant | MODIFIER | c.2638+2479_2638+248 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | ||||||
chr17:47432399 | A | AAAATAAA others(1): Show |
85 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0076 others(82): Show |
85 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.2638+2475_2638+248 others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | ||||||
chr17:47432399 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0180 a0001c0001t0001g0182 |
3 | HG01884.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2638+2471_2638+248 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | ||||||
chr17:47432399 | AAAATAAA others(5): Show |
A | 38 | a0001c0001t0005g0255 a0003c0004t0001g0141 a0004c0003t0001g0001 others(35): Show |
41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+2471_2638+248 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | ||||||
chr17:47432399 | AAAATAAA others(9): Show |
A | 44 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(41): Show |
45 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2638+2467_2638+248 others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | ||||||
chr17:47432845 | G | A | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+2884G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432845 | |||||||
chr17:47433224 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2638+3263C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433224 | |||||||
chr17:47433240 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+3279A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433240 | |||||||
chr17:47433354 | G | A | 1 | a0003c0004t0002g0232 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2638+3393G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433354 | |||||||
chr17:47433426 | C | CAAG | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+3471_2638+347 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47433426 | ||||||
chr17:47433452 | A | G | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+3491A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433452 | |||||||
chr17:47433605 | G | A | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+3644G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433605 | |||||||
chr17:47433631 | T | C | 2 | a0003c0004t0002g0224 a0003c0004t0002g0251 |
2 | NA18964.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2638+3670T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433631 | |||||||
chr17:47433713 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+3752T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433713 | |||||||
chr17:47433873 | T | G | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2638+3912T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433873 | |||||||
chr17:47433981 | T | TTG | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+4022_2638+402 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47433981 | ||||||
chr17:47434022 | C | T | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2638+4061C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434022 | |||||||
chr17:47434093 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2638+4132A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434093 | |||||||
chr17:47434182 | T | C | 34 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(31): Show |
37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.2638+4221T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434182 | |||||||
chr17:47434314 | C | CA | 13 | a0001c0001t0001g0111 a0001c0006t0001g0093 a0001c0006t0001g0094 others(10): Show |
13 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2638+4363dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47434314 | ||||||
chr17:47434314 | CA | C | 82 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(79): Show |
86 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.2638+4363delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47434314 | ||||||
chr17:47434321 | A | T | 6 | a0001c0001t0001g0185 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG00280.hp1 HG01106.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+4360A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434321 | |||||||
chr17:47434322 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2638+4361A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434322 | |||||||
chr17:47434325 | T | A | 63 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(60): Show |
63 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.2638+4364T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434325 | |||||||
chr17:47434328 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+4367A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434328 | |||||||
chr17:47434759 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+4798C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434759 | |||||||
chr17:47434774 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2638+4813A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434774 | |||||||
chr17:47434807 | C | T | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+4846C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434807 | |||||||
chr17:47435046 | A | C | 1 | a0003c0004t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2638+5085A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435046 | |||||||
chr17:47435117 | A | G | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.2638+5156A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435117 | |||||||
chr17:47435376 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0107 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2639-5055C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435376 | |||||||
chr17:47435380 | A | G | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2639-5051A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435380 | |||||||
chr17:47435555 | T | C | 3 | a0003c0008t0004g0011 a0003c0008t0004g0012 a0003c0008t0004g0053 |
3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2639-4876T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435555 | |||||||
chr17:47435593 | T | C | 2 | a0003c0004t0002g0246 a0003c0004t0002g0249 |
2 | NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2639-4838T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435593 | |||||||
chr17:47435683 | A | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2639-4748A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435683 | |||||||
chr17:47435723 | C | CAT | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2639-4707_2639-470 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47435723 | ||||||
chr17:47435726 | C | T | 39 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(36): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2639-4705C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435726 | |||||||
chr17:47435875 | G | A | 2 | a0005c0005t0003g0117 a0011c0027t0001g0121 |
2 | HG01123.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2639-4556G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435875 | |||||||
chr17:47435910 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
19 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2639-4521C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435910 | |||||||
chr17:47435913 | C | T | 3 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2639-4518C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435913 | |||||||
chr17:47435926 | A | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2639-4505A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435926 | |||||||
chr17:47435943 | C | T | 1 | a0004c0003t0001g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2639-4488C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435943 | |||||||
chr17:47435967 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-4464C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435967 | |||||||
chr17:47436031 | T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-4400T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436031 | |||||||
chr17:47436226 | G | A | 1 | a0014c0018t0001g0337 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2639-4205G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436226 | |||||||
chr17:47436565 | T | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-3866T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436565 | |||||||
chr17:47436830 | G | C | 36 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(33): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2639-3601G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436830 | |||||||
chr17:47436839 | G | A | 1 | a0003c0008t0004g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2639-3592G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436839 | |||||||
chr17:47437053 | T | A | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2639-3378T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437053 | |||||||
chr17:47437397 | C | G | 11 | a0001c0006t0001g0093 a0001c0006t0001g0094 a0001c0006t0001g0095 others(8): Show |
11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2639-3034C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437397 | |||||||
chr17:47437536 | G | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-2895G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437536 | |||||||
chr17:47437537 | C | T | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-2894C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437537 | |||||||
chr17:47437801 | A | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2639-2630A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437801 | |||||||
chr17:47438008 | T | A | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-2423T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438008 | |||||||
chr17:47438089 | G | A | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-2342G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438089 | |||||||
chr17:47438158 | T | C | 1 | a0003c0004t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-2273T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438158 | |||||||
chr17:47438312 | T | G | 233 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2639-2119T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438312 | |||||||
chr17:47438325 | G | A | 2 | a0008c0011t0001g0049 a0008c0011t0001g0050 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2639-2106G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438325 | |||||||
chr17:47438417 | T | G | 34 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(31): Show |
37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.2639-2014T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438417 | |||||||
chr17:47438453 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2639-1978A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438453 | |||||||
chr17:47438498 | C | CT | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.2639-1919dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47438498 | ||||||
chr17:47438498 | CT | C | 76 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(73): Show |
80 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2639-1919delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47438498 | ||||||
chr17:47438720 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2639-1711G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438720 | |||||||
chr17:47438744 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0003c0008t0001g0134 |
3 | NA18956.hp2 NA18960.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2639-1687T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438744 | |||||||
chr17:47438768 | T | C | 6 | a0003c0008t0004g0005 a0003c0008t0004g0011 a0003c0008t0004g0012 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2639-1663T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438768 | |||||||
chr17:47438830 | G | A | 1 | a0002c0002t0003g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2639-1601G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438830 | |||||||
chr17:47439171 | G | GT | 113 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2639-1236dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | ||||||
chr17:47439171 | G | GTT | 41 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0087 others(38): Show |
41 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-1237_2639-123 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | ||||||
chr17:47439171 | G | GTTT | 6 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0001g0111 others(3): Show |
6 | HG01175.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2639-1238_2639-123 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | ||||||
chr17:47439171 | GTTTTTTT others(5): Show |
G | 41 | a0004c0003t0001g0001 a0004c0003t0001g0003 a0004c0003t0001g0020 others(38): Show |
44 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2639-1247_2639-123 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | ||||||
chr17:47439177 | T | TG | 37 | a0003c0004t0002g0109 a0003c0004t0002g0214 a0003c0004t0002g0216 others(34): Show |
38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2639-1254_2639-125 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439177 | |||||||
chr17:47439198 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2639-1233A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439198 | |||||||
chr17:47439199 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2639-1232C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439199 | |||||||
chr17:47439301 | C | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.2639-1130C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439301 | |||||||
chr17:47439514 | C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-917C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439514 | |||||||
chr17:47439654 | C | T | 9 | a0006c0007t0001g0059 a0006c0007t0001g0060 a0006c0007t0001g0062 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-777C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439654 | |||||||
chr17:47439935 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2639-496T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439935 | |||||||
chr17:47440073 | A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-358A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440073 | |||||||
chr17:47440337 | A | C | 40 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(37): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-94A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440337 | |||||||
chr17:47440405 | T | A | 81 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(78): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2639-26T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440405 | |||||||
chr17:47440408 | G | T | 87 | a0003c0004t0001g0141 a0003c0004t0002g0109 a0003c0004t0002g0214 others(84): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2639-23G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440408 |