Item | Value |
---|---|
geneid | 9619 |
ensemblid | ENSG00000160179.19 |
hgncid | 73 |
symbol | ABCG1 |
name | ATP binding cassette subfamily G member 1 |
refseq_nuc | NM_016818.3 |
refseq_prot | NP_058198.2 |
ensembl_nuc | ENST00000398449.8 |
ensembl_prot | ENSP00000381467.3 |
mane_status | MANE Select |
chr | chr21 |
start | 42219140 |
end | 42297244 |
strand | + |
ver | v1.2 |
region | chr21:42219140-42297244 |
region5000 | chr21:42214140-42302244 |
regionname0 | ABCG1_chr21_42219140_42297244 |
regionname5000 | ABCG1_chr21_42214140_42302244 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 666 | 351 | 94 | 74 | 124 | 18 | 39 | 82 | ABCG1_chr21_42214140_42302244 | ABCG1 | MACLM others(661): Show |
chr21 | 42214140 | 42302244 |
a0002 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | MACLM others(661): Show |
chr21 | 42214140 | 42302244 |
a0003 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | MACLM others(661): Show |
chr21 | 42214140 | 42302244 |
a0004 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | MACLM others(661): Show |
chr21 | 42214140 | 42302244 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1998 | 314 | 75 | 69 | 113 | 17 | 38 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0002 | 0/0 | 1998 | 13 | 13 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0003 | 0/0 | 1998 | 10 | 0 | 2 | 8 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0004 | 0/0 | 1998 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0005 | 0/0 | 1998 | 3 | 1 | 0 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0006 | 0/0 | 1998 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0007 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0008 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0011 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0001c0012 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0002c0009 | 0/0 | 1998 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0003c0010 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 | ||
a0004c0013 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | ATGGC others(1993): Show |
chr21 | 42214140 | 42302244 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2976 | 76 | 18 | 11 | 37 | 5 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0002 | 0/1 | 2977 | 69 | 7 | 18 | 29 | 6 | 8 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2972): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0003 | 0/0 | 2978 | 50 | 7 | 13 | 17 | 3 | 10 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2973): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0004 | 0/0 | 2976 | 29 | 23 | 6 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0005 | 0/0 | 2971 | 18 | 0 | 3 | 12 | 1 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2966): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0006 | 0/0 | 2970 | 18 | 2 | 1 | 11 | 0 | 4 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0007 | 0/0 | 2972 | 10 | 1 | 1 | 5 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2967): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0008 | 0/0 | 2976 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0009 | 0/0 | 2977 | 6 | 5 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2972): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0010 | 0/0 | 2979 | 6 | 0 | 4 | 0 | 2 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2974): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0011 | 0/0 | 2970 | 4 | 0 | 4 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0012 | 0/0 | 2983 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2978): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0013 | 0/0 | 2978 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2973): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0014 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0015 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0017 | 0/0 | 2984 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2979): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0018 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0020 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2966): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0021 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0022 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0023 | 0/0 | 2974 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2969): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0024 | 0/0 | 2975 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2970): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0025 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2972): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0026 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2974): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0027 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0028 | 0/0 | 2982 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2977): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0029 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2977): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0030 | 0/0 | 2994 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2989): Show |
chr21 | 42214140 | 42302244 |
a0001c0001t0031 | 0/0 | 2996 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2991): Show |
chr21 | 42214140 | 42302244 |
a0001c0002t0002 | 0/0 | 2977 | 9 | 9 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2972): Show |
chr21 | 42214140 | 42302244 |
a0001c0002t0004 | 0/0 | 2976 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0002t0016 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0003 | 0/0 | 2978 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2973): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0005 | 0/0 | 2971 | 3 | 0 | 1 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2966): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0006 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0007 | 0/0 | 2972 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2967): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0008 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0003t0019 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0004t0003 | 0/0 | 2978 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2973): Show |
chr21 | 42214140 | 42302244 |
a0001c0005t0008 | 0/0 | 2976 | 3 | 1 | 0 | 0 | 1 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0006t0001 | 0/0 | 2976 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0006t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0007t0015 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0007t0016 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2968): Show |
chr21 | 42214140 | 42302244 |
a0001c0008t0011 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2965): Show |
chr21 | 42214140 | 42302244 |
a0001c0011t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0001c0012t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0002c0009t0003 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2973): Show |
chr21 | 42214140 | 42302244 |
a0003c0010t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
a0004c0013t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | GGAGC others(2971): Show |
chr21 | 42214140 | 42302244 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0009g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0010g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0010g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0010g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0011g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0011g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0011g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0012g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0012g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0013g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0013g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0013g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0015g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0017g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0018g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0020g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0022g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0023g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0024g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0025g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0026g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0027g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0028g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0029g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0030g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0001t0031g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0002t0016g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0003t0019g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0004t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0005t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0005t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0005t0008g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0006t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0006t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0007t0015g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0007t0016g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0008t0011g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0011t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0001c0012t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0002c0009t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0003c0010t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
a0004c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00099 | hp2 | a0001 | c0005 | t0008 | g0131 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | FIN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00408 | hp1 | a0001 | c0003 | t0005 | g0050 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0259 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | CHS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0194 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01069 | hp1 | a0001 | c0001 | t0012 | g0305 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01070 | hp2 | a0001 | c0006 | t0001 | g0008 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01071 | hp1 | a0001 | c0006 | t0001 | g0008 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0327 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01109 | hp2 | a0001 | c0001 | t0017 | g0007 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0195 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01243 | hp1 | a0001 | c0001 | t0025 | g0072 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0021 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01257 | hp2 | a0001 | c0001 | t0011 | g0045 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01346 | hp2 | a0001 | c0001 | t0023 | g0025 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0188 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01515 | hp2 | a0001 | c0001 | t0010 | g0301 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01517 | hp1 | a0001 | c0001 | t0010 | g0006 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | IBS | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01891 | hp2 | a0001 | c0005 | t0008 | g0170 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01934 | hp2 | a0001 | c0008 | t0011 | g0046 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01975 | hp2 | a0001 | c0003 | t0008 | g0119 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01978 | hp1 | a0001 | c0001 | t0011 | g0047 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01981 | hp2 | a0001 | c0001 | t0010 | g0167 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0344 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02004 | hp1 | a0001 | c0001 | t0027 | g0342 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02015 | hp2 | a0001 | c0003 | t0019 | g0031 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0331 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02132 | hp1 | a0001 | c0003 | t0006 | g0041 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02148 | hp1 | a0001 | c0003 | t0005 | g0044 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | CDX | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0059 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02280 | hp1 | a0001 | c0006 | t0004 | g0319 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02293 | hp1 | a0001 | c0001 | t0011 | g0042 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02293 | hp2 | a0001 | c0001 | t0022 | g0024 | AMR | PEL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0328 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | KHV | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02602 | hp1 | a0002 | c0009 | t0003 | g0258 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0294 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02615 | hp2 | a0001 | c0002 | t0016 | g0341 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0313 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0287 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0285 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0048 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0295 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0063 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0275 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0065 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0321 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0320 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0330 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0067 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03098 | hp2 | a0001 | c0001 | t0026 | g0316 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0007 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0334 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03490 | hp1 | a0001 | c0005 | t0008 | g0312 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03490 | hp2 | a0001 | c0001 | t0012 | g0140 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03491 | hp1 | a0001 | c0001 | t0009 | g0221 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03491 | hp2 | a0001 | c0001 | t0007 | g0029 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0028 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0141 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03516 | hp1 | a0001 | c0007 | t0015 | g0346 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03516 | hp2 | a0001 | c0007 | t0016 | g0345 | AFR | ESN | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03540 | hp1 | a0001 | c0011 | t0004 | g0089 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0058 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0296 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03704 | hp1 | a0001 | c0001 | t0028 | g0304 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0022 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | BEB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | STU | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0322 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0274 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0337 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0211 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18962 | hp1 | a0001 | c0001 | t0020 | g0017 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18981 | hp2 | a0001 | c0003 | t0005 | g0054 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18989 | hp1 | a0001 | c0001 | t0021 | g0010 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19003 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19004 | hp1 | a0001 | c0004 | t0003 | g0076 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19067 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19067 | hp2 | a0003 | c0010 | t0001 | g0249 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19070 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19087 | hp2 | a0004 | c0013 | t0001 | g0101 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19091 | hp1 | a0001 | c0003 | t0007 | g0056 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0096 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA19240 | hp2 | a0001 | c0012 | t0004 | g0276 | AFR | YRI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ASW | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0302 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0299 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0018 | SAS | GIH | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0292 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0144 | AMR | CLM | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02486 | hp1 | a0001 | c0001 | t0024 | g0103 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02559 | hp1 | a0001 | c0001 | t0030 | g0310 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | ACB | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG03471 | hp2 | a0001 | c0001 | t0029 | g0262 | AFR | MSL | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0329 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0343 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
NA21309 | hp2 | a0001 | c0001 | t0031 | g0079 | AFR | LWK | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0187 | REF | REF | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0160 | REF | REF | ABCG1_chr21_42214140_42302244 | ABCG1 | chr21 | 42214140 | 42302244 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:42225697 | G | T | 1 | a0004 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.69G>T | p.Met23Ile | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 192/2976 | 69/2001 | 23/666 | chr21 | 42225697 | |||
chr21:42225779 | G | A | 1 | a0002 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.151G>A | p.Gly51Arg | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 274/2976 | 151/2001 | 51/666 | chr21 | 42225779 | |||
chr21:42287931 | G | A | 1 | a0003 | 1 | NA19067.hp2 | missense_variant | MODERATE | c.1016G>A | p.Arg339Gln | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/15 | 1139/2976 | 1016/2001 | 339/666 | chr21 | 42287931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:42219271 | T | C | 1 | a0001c0007 | 2 | HG03516.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.9T>C | p.Cys3Cys | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 132/2976 | 9/2001 | 3/666 | chr21 | 42219271 | |||
chr21:42225724 | G | A | 1 | a0001c0008 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.96G>A | p.Ser32Ser | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/15 | 219/2976 | 96/2001 | 32/666 | chr21 | 42225724 | |||
chr21:42271122 | G | A | 1 | a0001c0003 | 10 | HG00408.hp1 HG00558.hp1 HG01975.hp2 others(7): Show |
synonymous_variant | LOW | c.339G>A | p.Leu113Leu | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/15 | 462/2976 | 339/2001 | 113/666 | chr21 | 42271122 | |||
chr21:42273345 | C | G | 1 | a0001c0006 | 3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.447C>G | p.Pro149Pro | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/15 | 570/2976 | 447/2001 | 149/666 | chr21 | 42273345 | |||
chr21:42287908 | C | T | 1 | a0001c0005 | 3 | HG00099.hp2 HG01891.hp2 HG03490.hp1 |
synonymous_variant | LOW | c.993C>T | p.Gly331Gly | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/15 | 1116/2976 | 993/2001 | 331/666 | chr21 | 42287908 | |||
chr21:42288312 | G | A | 1 | a0001c0011 | 1 | HG03540.hp1 | splice_region_variant&synonymous_variant | LOW | c.1224G>A | p.Ser408Ser | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/15 | 1347/2976 | 1224/2001 | 408/666 | chr21 | 42288312 | |||
chr21:42290193 | G | C | 1 | a0001c0002 | 13 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
synonymous_variant | LOW | c.1368G>C | p.Ala456Ala | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/15 | 1491/2976 | 1368/2001 | 456/666 | chr21 | 42290193 | |||
chr21:42294610 | C | T | 1 | a0001c0004 | 3 | NA19003.hp2 NA19004.hp1 NA19070.hp2 |
synonymous_variant | LOW | c.1722C>T | p.Phe574Phe | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/15 | 1845/2976 | 1722/2001 | 574/666 | chr21 | 42294610 | |||
chr21:42296233 | C | T | 1 | a0001c0012 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1842C>T | p.Asp614Asp | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 1965/2976 | 1842/2001 | 614/666 | chr21 | 42296233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:42219222 | C | CCCGCCG | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0028 others(1): Show |
8 | HG01069.hp1 HG01109.hp2 HG02630.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-9dupGCCGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 8 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | |||||
chr21:42219222 | C | CCCGCCGC others(11): Show |
2 | a0001c0001t0030 a0001c0001t0031 |
2 | HG02559.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-26_-9dupGCCGCCGCC others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 8 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | |||||
chr21:42219222 | CCCG | C | 7 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0023 others(4): Show |
7 | HG01346.hp2 HG02293.hp2 HG02486.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-11_-9delGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 9 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | |||||
chr21:42219222 | CCCGCCG | C | 13 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(10): Show |
62 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-9delGCCGCC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/15 | 9 | INFO_REALIGN_3_PRIME | chr21 | 42219222 | |||||
chr21:42296444 | G | A | 6 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0022 others(3): Show |
13 | HG00099.hp2 HG00741.hp1 HG01192.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*52G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 52 | chr21 | 42296444 | ||||||
chr21:42296450 | A | C | 1 | a0001c0001t0027 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 58 | chr21 | 42296450 | ||||||
chr21:42296473 | C | T | 1 | a0001c0001t0013 | 3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*81C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 81 | chr21 | 42296473 | ||||||
chr21:42296478 | G | A | 1 | a0001c0001t0018 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 86 | chr21 | 42296478 | ||||||
chr21:42296538 | G | A | 1 | a0001c0003t0019 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 146 | chr21 | 42296538 | ||||||
chr21:42296567 | G | A | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 175 | chr21 | 42296567 | ||||||
chr21:42296624 | G | GT | 9 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(6): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*245dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | |||||
chr21:42296624 | G | GTT | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(7): Show |
74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*244_*245dupTT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | |||||
chr21:42296624 | G | GTTT | 3 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0026 |
8 | HG00642.hp1 HG01123.hp1 HG01123.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*243_*245dupTTT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 246 | INFO_REALIGN_3_PRIME | chr21 | 42296624 | |||||
chr21:42296791 | A | G | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 399 | chr21 | 42296791 | ||||||
chr21:42297077 | C | T | 1 | a0001c0001t0020 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 15/15 | 685 | chr21 | 42297077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:42219366 | C | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.42+62C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219366 | |||||||
chr21:42219406 | G | T | 3 | a0001c0001t0003g0344 a0001c0001t0008g0343 a0001c0001t0027g0342 |
3 | HG01993.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.42+102G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219406 | |||||||
chr21:42219443 | T | A | 62 | a0001c0001t0005g0001 a0001c0001t0005g0011 a0001c0001t0005g0012 others(59): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+139T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219443 | |||||||
chr21:42219481 | A | C | 62 | a0001c0001t0005g0001 a0001c0001t0005g0011 a0001c0001t0005g0012 others(59): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+177A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219481 | |||||||
chr21:42219631 | C | G | 62 | a0001c0001t0005g0001 a0001c0001t0005g0011 a0001c0001t0005g0012 others(59): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+327C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219631 | |||||||
chr21:42219691 | G | A | 5 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0073 others(2): Show |
5 | HG00735.hp2 HG01106.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+387G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219691 | |||||||
chr21:42219733 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.42+429T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219733 | |||||||
chr21:42219897 | C | T | 1 | a0001c0002t0016g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.42+593C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219897 | |||||||
chr21:42219956 | C | G | 63 | a0001c0001t0001g0340 a0001c0001t0005g0001 a0001c0001t0005g0011 others(60): Show |
64 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.42+652C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42219956 | |||||||
chr21:42220059 | T | C | 62 | a0001c0001t0005g0001 a0001c0001t0005g0011 a0001c0001t0005g0012 others(59): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+755T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220059 | |||||||
chr21:42220073 | G | A | 62 | a0001c0001t0005g0001 a0001c0001t0005g0011 a0001c0001t0005g0012 others(59): Show |
63 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.42+769G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220073 | |||||||
chr21:42220307 | G | A | 2 | a0001c0001t0002g0077 a0001c0004t0003g0076 |
2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.42+1003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220307 | |||||||
chr21:42220320 | C | T | 2 | a0001c0001t0002g0338 a0001c0001t0002g0339 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.42+1016C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220320 | |||||||
chr21:42220334 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42+1030T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220334 | |||||||
chr21:42220415 | T | G | 2 | a0001c0001t0031g0079 a0001c0002t0002g0080 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.42+1111T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220415 | |||||||
chr21:42220421 | G | GA | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0002g0082 others(3): Show |
7 | HG01081.hp2 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+1129dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220421 | ||||||
chr21:42220421 | GA | G | 30 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0325 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.42+1129delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220421 | ||||||
chr21:42220593 | G | T | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42+1289G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220593 | |||||||
chr21:42220606 | G | A | 15 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.42+1302G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220606 | |||||||
chr21:42220854 | GTTATAGA others(3): Show |
G | 1 | a0004c0013t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.42+1552_42+1561del others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42220854 | ||||||
chr21:42220999 | T | C | 1 | a0001c0001t0003g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.42+1695T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42220999 | |||||||
chr21:42221237 | G | A | 66 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0005g0001 others(63): Show |
67 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.42+1933G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221237 | |||||||
chr21:42221258 | C | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0004g0334 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1954C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221258 | |||||||
chr21:42221283 | G | A | 1 | a0001c0001t0024g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+1979G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221283 | |||||||
chr21:42221348 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.42+2044C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221348 | |||||||
chr21:42221475 | A | T | 25 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0325 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.42+2171A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221475 | |||||||
chr21:42221495 | G | A | 44 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0110 others(41): Show |
46 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.42+2191G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221495 | |||||||
chr21:42221547 | G | A | 65 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0005g0001 others(62): Show |
66 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.42+2243G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221547 | |||||||
chr21:42221563 | A | G | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42+2259A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221563 | |||||||
chr21:42221603 | A | T | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+2299A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221603 | |||||||
chr21:42221864 | G | A | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+2560G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221864 | |||||||
chr21:42221949 | A | G | 1 | a0001c0001t0030g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.42+2645A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42221949 | |||||||
chr21:42222166 | T | A | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.42+2862T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222166 | |||||||
chr21:42222317 | C | T | 2 | a0001c0001t0003g0308 a0001c0001t0004g0309 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.42+3013C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222317 | |||||||
chr21:42222328 | C | T | 46 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0110 others(43): Show |
48 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.42+3024C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222328 | |||||||
chr21:42222477 | C | G | 1 | a0001c0001t0002g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.42+3173C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222477 | |||||||
chr21:42222552 | T | C | 1 | a0001c0001t0004g0311 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43-3119T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222552 | |||||||
chr21:42222646 | T | C | 3 | a0001c0001t0003g0318 a0001c0001t0004g0317 a0001c0001t0026g0316 |
3 | HG02572.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.43-3025T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222646 | |||||||
chr21:42222700 | G | A | 2 | a0001c0001t0012g0140 a0001c0001t0012g0141 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.43-2971G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222700 | |||||||
chr21:42222753 | G | A | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-2918G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222753 | |||||||
chr21:42222937 | A | C | 136 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(133): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.43-2734A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222937 | |||||||
chr21:42222990 | T | G | 73 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(70): Show |
77 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-2681T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42222990 | |||||||
chr21:42223154 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0003g0261 |
2 | NA18977.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.43-2517C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223154 | |||||||
chr21:42223172 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0002g0306 a0001c0001t0012g0140 others(4): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-2499C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223172 | |||||||
chr21:42223178 | G | A | 1 | a0001c0001t0005g0001 | 2 | NA18973.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.43-2493G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223178 | |||||||
chr21:42223328 | C | T | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.43-2343C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223328 | |||||||
chr21:42223473 | G | A | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43-2198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223473 | |||||||
chr21:42223473 | G | C | 33 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(30): Show |
35 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.43-2198G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223473 | |||||||
chr21:42223481 | G | T | 146 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0098 others(143): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.43-2190G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223481 | |||||||
chr21:42223505 | C | T | 1 | a0001c0001t0009g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43-2166C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223505 | |||||||
chr21:42223668 | A | T | 2 | a0001c0001t0007g0028 a0001c0001t0007g0029 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.43-2003A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223668 | |||||||
chr21:42223681 | G | A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0006g0013 |
3 | NA18612.hp1 NA18939.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.43-1990G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223681 | |||||||
chr21:42223899 | T | C | 182 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(179): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.43-1772T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223899 | |||||||
chr21:42223917 | C | T | 102 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0142 others(99): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.43-1754C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223917 | |||||||
chr21:42223956 | C | G | 2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.43-1715C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42223956 | |||||||
chr21:42224164 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.43-1507G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224164 | |||||||
chr21:42224167 | T | C | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.43-1504T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224167 | |||||||
chr21:42224197 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.43-1474C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224197 | |||||||
chr21:42224221 | T | C | 181 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(178): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.43-1450T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224221 | |||||||
chr21:42224275 | T | C | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.43-1396T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224275 | |||||||
chr21:42224308 | G | A | 1 | a0001c0001t0030g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.43-1363G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224308 | |||||||
chr21:42224317 | C | T | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-1354C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224317 | |||||||
chr21:42224424 | C | T | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.43-1247C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224424 | |||||||
chr21:42224477 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.43-1194G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224477 | |||||||
chr21:42224520 | G | C | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-1151G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224520 | |||||||
chr21:42224614 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.43-1057C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224614 | |||||||
chr21:42224763 | A | G | 1 | a0001c0002t0004g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.43-908A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42224763 | |||||||
chr21:42224944 | C | CT | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0002g0303 others(6): Show |
9 | HG00140.hp1 HG01975.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.43-713dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42224944 | ||||||
chr21:42224944 | CT | C | 25 | a0001c0001t0001g0155 a0001c0001t0001g0325 a0001c0001t0001g0326 others(22): Show |
26 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.43-713delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr21 | 42224944 | ||||||
chr21:42225096 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.43-575T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225096 | |||||||
chr21:42225202 | T | C | 2 | a0001c0001t0012g0305 a0001c0001t0028g0304 |
2 | HG01069.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-469T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225202 | |||||||
chr21:42225319 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.43-352T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225319 | |||||||
chr21:42225613 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.43-58T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 1/14 | chr21 | 42225613 | |||||||
chr21:42225918 | G | A | 4 | a0001c0001t0005g0001 a0001c0001t0005g0016 a0001c0001t0005g0068 others(1): Show |
5 | HG02129.hp2 NA18962.hp1 NA18969.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.286+4G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225918 | |||||||
chr21:42225925 | C | T | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+11C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225925 | |||||||
chr21:42225960 | G | A | 1 | a0001c0001t0006g0014 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.286+46G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42225960 | |||||||
chr21:42226215 | G | C | 1 | a0001c0001t0010g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.286+301G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226215 | |||||||
chr21:42226272 | C | A | 1 | a0004c0013t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+358C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226272 | |||||||
chr21:42226316 | C | T | 6 | a0001c0001t0001g0263 a0001c0001t0002g0267 a0001c0001t0004g0264 others(3): Show |
6 | HG01261.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+402C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226316 | |||||||
chr21:42226490 | C | T | 1 | a0001c0001t0005g0069 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.286+576C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226490 | |||||||
chr21:42226606 | G | A | 1 | a0001c0003t0019g0031 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.286+692G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226606 | |||||||
chr21:42226632 | T | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0314 a0001c0001t0009g0087 |
3 | HG02145.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286+718T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226632 | |||||||
chr21:42226696 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+782T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226696 | |||||||
chr21:42226716 | G | A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+802G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226716 | |||||||
chr21:42226717 | A | T | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+803A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226717 | |||||||
chr21:42226884 | G | A | 4 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+970G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42226884 | |||||||
chr21:42227340 | A | G | 33 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0126 others(30): Show |
35 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.286+1426A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227340 | |||||||
chr21:42227408 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+1494A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227408 | |||||||
chr21:42227454 | T | C | 4 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+1540T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227454 | |||||||
chr21:42227638 | G | A | 37 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0126 others(34): Show |
39 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+1724G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227638 | |||||||
chr21:42227748 | G | A | 4 | a0001c0001t0001g0155 a0001c0001t0003g0153 a0001c0001t0004g0154 others(1): Show |
4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1834G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227748 | |||||||
chr21:42227757 | G | T | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286+1843G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227757 | |||||||
chr21:42227839 | GGAGA | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0004g0269 others(2): Show |
5 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+1939_286+1942d others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42227839 | ||||||
chr21:42227842 | G | T | 2 | a0001c0001t0001g0336 a0001c0001t0004g0334 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286+1928G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227842 | |||||||
chr21:42227848 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.286+1934G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227848 | |||||||
chr21:42227984 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286+2070G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42227984 | |||||||
chr21:42228028 | C | T | 1 | a0002c0009t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.286+2114C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228028 | |||||||
chr21:42228033 | C | T | 4 | a0001c0001t0004g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 others(1): Show |
4 | HG01081.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+2119C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228033 | |||||||
chr21:42228256 | G | A | 67 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0260 others(64): Show |
68 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.286+2342G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228256 | |||||||
chr21:42228313 | A | G | 185 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(182): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2399A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228313 | |||||||
chr21:42228320 | C | G | 185 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(182): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2406C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228320 | |||||||
chr21:42228443 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0004g0283 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.286+2529C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228443 | |||||||
chr21:42228628 | G | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+2714G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228628 | |||||||
chr21:42228643 | C | A | 15 | a0001c0001t0001g0155 a0001c0001t0001g0325 a0001c0001t0001g0326 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+2729C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228643 | |||||||
chr21:42228825 | G | C | 185 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(182): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.286+2911G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42228825 | |||||||
chr21:42229062 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+3148A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229062 | |||||||
chr21:42229105 | G | A | 2 | a0001c0001t0004g0158 a0001c0002t0002g0143 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.286+3191G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229105 | |||||||
chr21:42229264 | T | G | 1 | a0001c0001t0027g0342 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.286+3350T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229264 | |||||||
chr21:42229284 | T | C | 4 | a0001c0001t0001g0155 a0001c0001t0003g0153 a0001c0001t0004g0154 others(1): Show |
4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3370T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229284 | |||||||
chr21:42229442 | G | A | 2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.286+3528G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229442 | |||||||
chr21:42229457 | C | G | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.286+3543C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229457 | |||||||
chr21:42229501 | C | T | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+3587C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229501 | |||||||
chr21:42229551 | C | G | 1 | a0001c0001t0003g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.286+3637C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229551 | |||||||
chr21:42229564 | A | C | 2 | a0001c0001t0001g0255 a0001c0001t0003g0256 |
2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.286+3650A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229564 | |||||||
chr21:42229588 | C | T | 1 | a0001c0002t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.286+3674C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229588 | |||||||
chr21:42229667 | T | C | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0323 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+3753T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229667 | |||||||
chr21:42229670 | G | C | 1 | a0001c0001t0005g0032 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.286+3756G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229670 | |||||||
chr21:42229674 | C | A | 4 | a0001c0001t0001g0155 a0001c0001t0003g0153 a0001c0001t0004g0154 others(1): Show |
4 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3760C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42229674 | |||||||
chr21:42229719 | C | CAA | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0323 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+3814_286+3815d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42229719 | ||||||
chr21:42230060 | T | C | 3 | a0001c0001t0001g0333 a0001c0001t0003g0308 a0001c0001t0004g0309 |
3 | HG02055.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.286+4146T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230060 | |||||||
chr21:42230081 | G | A | 3 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 |
3 | HG01496.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.286+4167G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230081 | |||||||
chr21:42230132 | A | T | 1 | a0001c0006t0004g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+4218A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230132 | |||||||
chr21:42230160 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0002g0106 a0001c0001t0002g0123 |
3 | NA18962.hp2 NA18989.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.286+4246G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230160 | |||||||
chr21:42230228 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.286+4314A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230228 | |||||||
chr21:42230277 | A | G | 184 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.286+4363A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230277 | |||||||
chr21:42230346 | A | G | 338 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(335): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.286+4432A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230346 | |||||||
chr21:42230362 | C | T | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0323 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4448C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230362 | |||||||
chr21:42230590 | G | A | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0323 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4676G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230590 | |||||||
chr21:42230620 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+4706G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230620 | |||||||
chr21:42230623 | A | T | 2 | a0001c0001t0001g0260 a0001c0001t0003g0261 |
2 | NA18977.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.286+4709A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230623 | |||||||
chr21:42230656 | C | A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+4742C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230656 | |||||||
chr21:42230666 | C | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0016 a0001c0001t0005g0026 others(3): Show |
7 | HG02129.hp2 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+4752C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230666 | |||||||
chr21:42230669 | G | A | 68 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0260 others(65): Show |
69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.286+4755G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230669 | |||||||
chr21:42230770 | C | T | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0323 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+4856C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230770 | |||||||
chr21:42230940 | G | A | 7 | a0001c0001t0001g0260 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+5026G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230940 | |||||||
chr21:42230948 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286+5034G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230948 | |||||||
chr21:42230952 | C | T | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0003c0010t0001g0249 |
3 | HG02056.hp1 NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.286+5038C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42230952 | |||||||
chr21:42231006 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.286+5092C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231006 | |||||||
chr21:42231189 | G | A | 2 | a0001c0001t0003g0153 a0001c0001t0004g0154 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.286+5275G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231189 | |||||||
chr21:42231191 | GC | G | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+5278delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231191 | |||||||
chr21:42231203 | A | G | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+5289A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231203 | |||||||
chr21:42231370 | C | T | 2 | a0001c0001t0022g0024 a0001c0001t0023g0025 |
2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.286+5456C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231370 | |||||||
chr21:42231412 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.286+5498C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231412 | |||||||
chr21:42231446 | C | T | 169 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(166): Show |
174 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.286+5532C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231446 | |||||||
chr21:42231481 | C | T | 2 | a0001c0001t0010g0006 a0001c0001t0010g0301 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.286+5567C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231481 | |||||||
chr21:42231486 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+5572T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231486 | |||||||
chr21:42231546 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0003g0071 a0001c0001t0003g0073 others(2): Show |
5 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+5632C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231546 | |||||||
chr21:42231566 | G | A | 2 | a0001c0001t0001g0314 a0001c0001t0009g0087 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.286+5652G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231566 | |||||||
chr21:42231567 | A | G | 1 | a0001c0001t0011g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.286+5653A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231567 | |||||||
chr21:42231595 | T | C | 190 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(187): Show |
197 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.286+5681T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231595 | |||||||
chr21:42231626 | A | G | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+5712A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231626 | |||||||
chr21:42231736 | T | G | 4 | a0001c0001t0002g0291 a0001c0001t0002g0293 a0001c0001t0002g0303 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+5822T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231736 | |||||||
chr21:42231847 | C | T | 167 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(164): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.286+5933C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231847 | |||||||
chr21:42231861 | C | A | 1 | a0001c0001t0010g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286+5947C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231861 | |||||||
chr21:42231863 | T | C | 1 | a0001c0002t0004g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286+5949T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231863 | |||||||
chr21:42231991 | G | C | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+6077G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42231991 | |||||||
chr21:42232204 | T | A | 189 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(186): Show |
196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.286+6290T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232204 | |||||||
chr21:42232300 | C | T | 119 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(116): Show |
122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.286+6386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232300 | |||||||
chr21:42232397 | G | T | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0092 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+6483G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232397 | |||||||
chr21:42232420 | G | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+6506G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232420 | |||||||
chr21:42232672 | C | G | 124 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(121): Show |
127 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.286+6758C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232672 | |||||||
chr21:42232943 | C | T | 164 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(161): Show |
168 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.286+7029C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42232943 | |||||||
chr21:42233090 | C | G | 164 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(161): Show |
168 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.286+7176C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233090 | |||||||
chr21:42233340 | G | A | 3 | a0001c0001t0003g0344 a0001c0001t0008g0343 a0001c0001t0027g0342 |
3 | HG01993.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.286+7426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233340 | |||||||
chr21:42233347 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.286+7433G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233347 | |||||||
chr21:42233565 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.286+7651C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233565 | |||||||
chr21:42233951 | G | T | 20 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(17): Show |
22 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.286+8037G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233951 | |||||||
chr21:42233996 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+8082C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42233996 | |||||||
chr21:42234023 | G | GT | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0243 others(11): Show |
14 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+8118dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42234023 | ||||||
chr21:42234023 | GT | G | 171 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(168): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.286+8118delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42234023 | ||||||
chr21:42234585 | C | A | 4 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+8671C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234585 | |||||||
chr21:42234796 | G | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+8882G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234796 | |||||||
chr21:42234807 | C | T | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.286+8893C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234807 | |||||||
chr21:42234970 | C | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+9056C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42234970 | |||||||
chr21:42235109 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.286+9195C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235109 | |||||||
chr21:42235157 | G | A | 126 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.286+9243G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235157 | |||||||
chr21:42235158 | G | C | 4 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0334 others(1): Show |
4 | HG02055.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+9244G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235158 | |||||||
chr21:42235309 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0002g0164 |
2 | NA18971.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.286+9395G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235309 | |||||||
chr21:42235340 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.286+9426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235340 | |||||||
chr21:42235522 | T | C | 2 | a0001c0001t0002g0338 a0001c0001t0002g0339 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+9608T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235522 | |||||||
chr21:42235531 | C | T | 8 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0311 others(5): Show |
8 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+9617C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235531 | |||||||
chr21:42235540 | G | A | 2 | a0001c0001t0022g0024 a0001c0001t0023g0025 |
2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.286+9626G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235540 | |||||||
chr21:42235949 | G | T | 4 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+10035G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42235949 | |||||||
chr21:42236020 | T | C | 2 | a0001c0002t0002g0080 a0001c0002t0016g0341 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.286+10106T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236020 | |||||||
chr21:42236112 | G | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+10198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236112 | |||||||
chr21:42236181 | C | T | 5 | a0001c0001t0001g0260 a0001c0001t0002g0148 a0001c0001t0002g0150 others(2): Show |
5 | HG00423.hp1 HG00621.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+10267C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236181 | |||||||
chr21:42236241 | G | A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0326 others(11): Show |
15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+10327G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236241 | |||||||
chr21:42236375 | G | T | 8 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0311 others(5): Show |
8 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+10461G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236375 | |||||||
chr21:42236484 | A | T | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0253 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+10570A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236484 | |||||||
chr21:42236544 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0002g0122 a0001c0001t0003g0125 |
3 | HG02738.hp2 HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.286+10630G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236544 | |||||||
chr21:42236621 | T | C | 3 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.286+10707T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236621 | |||||||
chr21:42236724 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0006g0061 |
2 | HG02523.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.286+10810G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236724 | |||||||
chr21:42236826 | G | A | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+10912G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236826 | |||||||
chr21:42236971 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0335 |
2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286+11057G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42236971 | |||||||
chr21:42237048 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286+11134C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237048 | |||||||
chr21:42237138 | G | A | 124 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(121): Show |
129 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.286+11224G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237138 | |||||||
chr21:42237160 | T | G | 1 | a0001c0001t0003g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.286+11246T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237160 | |||||||
chr21:42237285 | T | G | 2 | a0001c0001t0003g0107 a0001c0001t0003g0108 |
2 | NA18939.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.286+11371T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237285 | |||||||
chr21:42237310 | A | G | 1 | a0001c0001t0026g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+11396A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237310 | |||||||
chr21:42237604 | C | G | 5 | a0001c0001t0005g0053 a0001c0001t0006g0055 a0001c0001t0007g0057 others(2): Show |
5 | NA18952.hp2 NA18980.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+11690C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237604 | |||||||
chr21:42237679 | C | G | 6 | a0001c0001t0001g0238 a0001c0001t0001g0340 a0001c0001t0002g0237 others(3): Show |
6 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+11765C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237679 | |||||||
chr21:42237705 | A | G | 4 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0002t0002g0080 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+11791A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237705 | |||||||
chr21:42237886 | C | T | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0253 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+11972C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42237886 | |||||||
chr21:42238005 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286+12091G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238005 | |||||||
chr21:42238096 | G | A | 151 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(148): Show |
157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.286+12182G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238096 | |||||||
chr21:42238116 | G | C | 188 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(185): Show |
195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12202G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238116 | |||||||
chr21:42238214 | T | G | 1 | a0001c0001t0014g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.286+12300T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238214 | |||||||
chr21:42238334 | T | C | 188 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(185): Show |
195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12420T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238334 | |||||||
chr21:42238380 | G | T | 1 | a0001c0001t0021g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.286+12466G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238380 | |||||||
chr21:42238391 | A | G | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+12477A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238391 | |||||||
chr21:42238398 | C | T | 188 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(185): Show |
195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12484C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238398 | |||||||
chr21:42238693 | C | T | 5 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0334 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+12779C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238693 | |||||||
chr21:42238748 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.286+12834C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238748 | |||||||
chr21:42238760 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.286+12846T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238760 | |||||||
chr21:42238869 | A | G | 188 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(185): Show |
195 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.286+12955A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238869 | |||||||
chr21:42238899 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286+12985T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238899 | |||||||
chr21:42238979 | G | A | 20 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(17): Show |
21 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+13065G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42238979 | |||||||
chr21:42239194 | C | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0003g0135 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13280C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239194 | |||||||
chr21:42239487 | G | A | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13573G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239487 | |||||||
chr21:42239518 | G | T | 2 | a0001c0001t0001g0235 a0001c0001t0002g0236 |
2 | HG00323.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.286+13604G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239518 | |||||||
chr21:42239530 | G | A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+13616G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239530 | |||||||
chr21:42239720 | T | C | 152 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(149): Show |
158 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.286+13806T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239720 | |||||||
chr21:42239866 | C | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+13952C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239866 | |||||||
chr21:42239870 | G | A | 5 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0334 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+13956G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239870 | |||||||
chr21:42239900 | G | A | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286+13986G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42239900 | |||||||
chr21:42240027 | G | A | 22 | a0001c0001t0001g0278 a0001c0001t0001g0325 a0001c0001t0002g0273 others(19): Show |
23 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+14113G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240027 | |||||||
chr21:42240169 | C | T | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0253 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+14255C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240169 | |||||||
chr21:42240183 | C | T | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+14269C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240183 | |||||||
chr21:42240203 | C | T | 13 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.286+14289C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240203 | |||||||
chr21:42240216 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+14302C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240216 | |||||||
chr21:42240481 | C | T | 137 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(134): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.286+14567C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240481 | |||||||
chr21:42240482 | G | T | 9 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0311 others(6): Show |
9 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14568G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240482 | |||||||
chr21:42240578 | G | A | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0253 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+14664G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240578 | |||||||
chr21:42240607 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0004g0334 others(1): Show |
4 | HG02055.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+14693C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240607 | |||||||
chr21:42240630 | T | C | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286+14716T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240630 | |||||||
chr21:42240662 | G | A | 2 | a0001c0001t0004g0158 a0001c0002t0002g0143 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.286+14748G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240662 | |||||||
chr21:42240694 | C | T | 3 | a0001c0001t0002g0233 a0001c0001t0003g0232 a0001c0001t0006g0030 |
3 | HG00558.hp2 NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.286+14780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240694 | |||||||
chr21:42240777 | G | A | 1 | a0001c0001t0003g0127 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.286+14863G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240777 | |||||||
chr21:42240936 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0002g0230 |
2 | HG00544.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.286+15022C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42240936 | |||||||
chr21:42241179 | G | A | 1 | a0001c0001t0006g0018 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.286+15265G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241179 | |||||||
chr21:42241271 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+15357G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241271 | |||||||
chr21:42241367 | G | A | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+15453G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241367 | |||||||
chr21:42241376 | G | A | 137 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(134): Show |
143 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.286+15462G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241376 | |||||||
chr21:42241510 | C | A | 5 | a0001c0001t0002g0306 a0001c0001t0012g0140 a0001c0001t0012g0141 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+15596C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241510 | |||||||
chr21:42241604 | CA | C | 125 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(122): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.286+15702delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241604 | ||||||
chr21:42241617 | T | A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+15703T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241617 | |||||||
chr21:42241620 | CA | C | 176 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(173): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.286+15716delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241620 | ||||||
chr21:42241705 | T | G | 1 | a0001c0003t0019g0031 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.286+15791T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241705 | |||||||
chr21:42241810 | C | A | 112 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(109): Show |
116 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.286+15896C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241810 | |||||||
chr21:42241820 | TA | T | 151 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(148): Show |
156 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.286+15920delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241820 | ||||||
chr21:42241862 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.286+15948C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241862 | |||||||
chr21:42241977 | C | CA | 24 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0110 others(21): Show |
24 | HG01070.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+16082dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241977 | C | CAA | 10 | a0001c0001t0001g0155 a0001c0001t0002g0122 a0001c0001t0002g0137 others(7): Show |
10 | HG01069.hp2 HG01167.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+16081_286+1608 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241977 | C | CAAA | 85 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(82): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.286+16080_286+1608 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241977 | C | CAAAA | 27 | a0001c0001t0001g0124 a0001c0001t0001g0278 a0001c0001t0001g0284 others(24): Show |
28 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.286+16079_286+1608 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241977 | C | CAAAAA | 7 | a0001c0001t0004g0327 a0001c0001t0007g0033 a0001c0002t0002g0328 others(4): Show |
7 | HG01081.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+16078_286+1608 others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241977 | CA | C | 6 | a0001c0001t0001g0271 a0001c0001t0002g0229 a0001c0001t0002g0306 others(3): Show |
7 | HG00099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+16082delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42241977 | ||||||
chr21:42241978 | A | G | 2 | a0001c0001t0012g0305 a0001c0001t0028g0304 |
2 | HG01069.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.286+16064A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241978 | |||||||
chr21:42241979 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.286+16065A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42241979 | |||||||
chr21:42242035 | T | C | 3 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.286+16121T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242035 | |||||||
chr21:42242213 | T | A | 3 | a0001c0001t0001g0155 a0001c0001t0003g0153 a0001c0001t0004g0154 |
3 | HG02257.hp1 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.286+16299T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242213 | |||||||
chr21:42242231 | C | T | 86 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0126 others(83): Show |
89 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.286+16317C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242231 | |||||||
chr21:42242380 | A | T | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286+16466A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242380 | |||||||
chr21:42242466 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.286+16552A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242466 | |||||||
chr21:42242484 | C | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.286+16570C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242484 | |||||||
chr21:42242516 | C | A | 148 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.286+16602C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242516 | |||||||
chr21:42242686 | C | T | 140 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(137): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+16772C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242686 | |||||||
chr21:42242721 | G | A | 5 | a0001c0001t0004g0182 a0001c0001t0004g0268 a0001c0001t0004g0311 others(2): Show |
5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+16807G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242721 | |||||||
chr21:42242970 | C | A | 5 | a0001c0001t0002g0183 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17056C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242970 | |||||||
chr21:42242971 | C | A | 5 | a0001c0001t0002g0183 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17057C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242971 | |||||||
chr21:42242972 | A | C | 5 | a0001c0001t0002g0183 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17058A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42242972 | |||||||
chr21:42243027 | C | A | 5 | a0001c0001t0004g0169 a0001c0001t0004g0182 a0001c0001t0004g0311 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17113C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243027 | |||||||
chr21:42243066 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286+17152C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243066 | |||||||
chr21:42243135 | C | G | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.286+17221C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243135 | |||||||
chr21:42243167 | T | G | 1 | a0001c0002t0002g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286+17253T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243167 | |||||||
chr21:42243208 | G | A | 23 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(20): Show |
25 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.286+17294G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243208 | |||||||
chr21:42243249 | C | A | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.286+17335C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243249 | |||||||
chr21:42243365 | A | G | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286+17451A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243365 | |||||||
chr21:42243435 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+17521C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243435 | |||||||
chr21:42243435 | CGT | C | 5 | a0001c0001t0001g0159 a0001c0001t0001g0314 a0001c0001t0002g0236 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+17529_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243435 | ||||||
chr21:42243441 | TGTGC | T | 91 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0133 others(88): Show |
94 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.286+17529_286+1753 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243441 | ||||||
chr21:42243443 | T | C | 10 | a0001c0001t0001g0142 a0001c0001t0001g0325 a0001c0001t0002g0181 others(7): Show |
10 | HG01167.hp1 HG01257.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+17529T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243443 | |||||||
chr21:42243443 | TGC | T | 63 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0155 others(60): Show |
65 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243443 | ||||||
chr21:42243445 | C | CGT | 8 | a0001c0001t0001g0248 a0001c0001t0001g0333 a0001c0001t0002g0219 others(5): Show |
8 | HG02055.hp2 HG02056.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+17532_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | ||||||
chr21:42243445 | C | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0325 a0001c0001t0002g0181 others(8): Show |
11 | HG01167.hp1 HG01257.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+17531C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243445 | |||||||
chr21:42243445 | CGCGT | C | 41 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0145 others(38): Show |
42 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | ||||||
chr21:42243445 | CGCGTGT | C | 9 | a0001c0001t0001g0165 a0001c0001t0002g0162 a0001c0001t0002g0164 others(6): Show |
10 | HG00408.hp2 HG00558.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+17533_286+1753 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | ||||||
chr21:42243445 | CGCGTGTG others(1): Show |
C | 20 | a0001c0001t0001g0091 a0001c0001t0001g0263 a0001c0001t0001g0326 others(17): Show |
20 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+17533_286+1754 others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | ||||||
chr21:42243445 | CGCGTGTG others(3): Show |
C | 2 | a0001c0001t0030g0310 a0001c0003t0006g0041 |
2 | HG02132.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.286+17533_286+1754 others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243445 | ||||||
chr21:42243447 | C | CGT | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0157 others(5): Show |
8 | HG02040.hp2 HG02080.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | ||||||
chr21:42243447 | C | CGTGT | 3 | a0001c0001t0002g0117 a0001c0001t0002g0217 a0001c0001t0002g0307 |
3 | HG02129.hp1 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.286+17573_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | ||||||
chr21:42243447 | C | T | 36 | a0001c0001t0001g0078 a0001c0001t0001g0142 a0001c0001t0001g0159 others(33): Show |
36 | HG00323.hp1 HG01106.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.286+17533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243447 | |||||||
chr21:42243447 | CGT | C | 21 | a0001c0001t0001g0126 a0001c0001t0001g0172 a0001c0001t0001g0191 others(18): Show |
21 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | ||||||
chr21:42243447 | CGTGT | C | 15 | a0001c0001t0001g0238 a0001c0001t0001g0290 a0001c0001t0001g0340 others(12): Show |
15 | HG00280.hp1 HG00280.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+17573_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | ||||||
chr21:42243447 | CGTGTGT | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0237 |
3 | HG00423.hp2 HG00741.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.286+17571_286+1757 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243447 | ||||||
chr21:42243451 | T | C | 4 | a0001c0001t0004g0169 a0001c0001t0004g0311 a0001c0001t0009g0320 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+17537T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243451 | |||||||
chr21:42243451 | T | TGC | 3 | a0001c0001t0001g0078 a0001c0001t0001g0335 a0001c0001t0012g0313 |
3 | HG02622.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.286+17538_286+1753 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243451 | ||||||
chr21:42243453 | T | C | 2 | a0001c0001t0004g0182 a0001c0001t0009g0275 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.286+17539T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243453 | |||||||
chr21:42243455 | T | C | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0155 others(16): Show |
21 | HG00738.hp2 HG01109.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+17541T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243455 | |||||||
chr21:42243457 | T | C | 6 | a0001c0001t0002g0254 a0001c0001t0002g0286 a0001c0001t0002g0288 others(3): Show |
6 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+17543T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243457 | |||||||
chr21:42243485 | TGTGTGC | T | 5 | a0001c0001t0001g0231 a0001c0001t0001g0260 a0001c0001t0002g0173 others(2): Show |
5 | NA18964.hp2 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+17573_286+1757 others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243485 | ||||||
chr21:42243487 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.286+17573T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243487 | |||||||
chr21:42243487 | TGTGC | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0297 a0001c0001t0002g0277 others(3): Show |
6 | HG01243.hp2 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+17575_286+1757 others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243487 | ||||||
chr21:42243489 | T | C | 15 | a0001c0001t0001g0192 a0001c0001t0003g0256 a0001c0001t0004g0169 others(12): Show |
15 | HG01346.hp2 HG02040.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+17575T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243489 | |||||||
chr21:42243489 | TGC | T | 30 | a0001c0001t0001g0133 a0001c0001t0001g0179 a0001c0001t0001g0235 others(27): Show |
31 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.286+17578_286+1757 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243489 | ||||||
chr21:42243491 | C | T | 66 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0142 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.286+17577C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243491 | |||||||
chr21:42243709 | G | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.286+17795G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243709 | |||||||
chr21:42243717 | G | T | 27 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0145 others(24): Show |
29 | HG00099.hp2 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.286+17803G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243717 | |||||||
chr21:42243751 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.286+17837A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243751 | |||||||
chr21:42243814 | C | CT | 96 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0155 others(93): Show |
97 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.286+17922dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | ||||||
chr21:42243814 | C | CTT | 18 | a0001c0001t0001g0093 a0001c0001t0001g0142 a0001c0001t0001g0214 others(15): Show |
18 | HG00642.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.286+17921_286+1792 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | ||||||
chr21:42243814 | CT | C | 40 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0145 others(37): Show |
43 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.286+17922delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42243814 | ||||||
chr21:42243850 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.286+17936A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243850 | |||||||
chr21:42243858 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+17944G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243858 | |||||||
chr21:42243966 | C | T | 2 | a0001c0001t0002g0306 a0001c0001t0028g0304 |
2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+18052C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243966 | |||||||
chr21:42243974 | A | G | 1 | a0001c0001t0002g0302 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+18060A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243974 | |||||||
chr21:42243975 | C | A | 6 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+18061C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42243975 | |||||||
chr21:42244066 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0243 |
2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.286+18152A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244066 | |||||||
chr21:42244067 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0243 |
2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.286+18153T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244067 | |||||||
chr21:42244146 | A | C | 1 | a0001c0001t0012g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+18232A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244146 | |||||||
chr21:42244536 | C | T | 2 | a0001c0001t0002g0306 a0001c0001t0028g0304 |
2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+18622C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244536 | |||||||
chr21:42244537 | T | A | 23 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(20): Show |
25 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.286+18623T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244537 | |||||||
chr21:42244542 | T | C | 4 | a0001c0001t0004g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 others(1): Show |
4 | HG01081.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+18628T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244542 | |||||||
chr21:42244668 | A | G | 6 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+18754A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244668 | |||||||
chr21:42244681 | C | G | 41 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0142 others(38): Show |
42 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.286+18767C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244681 | |||||||
chr21:42244681 | C | T | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0155 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+18767C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244681 | |||||||
chr21:42244756 | C | A | 1 | a0001c0001t0028g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+18842C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244756 | |||||||
chr21:42244803 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.286+18889G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244803 | |||||||
chr21:42244883 | C | T | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+18969C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244883 | |||||||
chr21:42244888 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.286+18974T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244888 | |||||||
chr21:42244914 | G | A | 20 | a0001c0001t0001g0278 a0001c0001t0001g0284 a0001c0001t0001g0314 others(17): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+19000G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42244914 | |||||||
chr21:42245078 | G | A | 9 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
9 | HG02056.hp1 NA18948.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+19164G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245078 | |||||||
chr21:42245092 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.286+19178G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245092 | |||||||
chr21:42245130 | G | A | 8 | a0001c0001t0002g0181 a0001c0001t0005g0043 a0001c0001t0011g0042 others(5): Show |
8 | HG01257.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+19216G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245130 | |||||||
chr21:42245179 | T | G | 1 | a0001c0001t0006g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+19265T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245179 | |||||||
chr21:42245194 | GA | G | 9 | a0001c0001t0001g0278 a0001c0001t0001g0314 a0001c0001t0002g0273 others(6): Show |
9 | HG01884.hp2 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+19282delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245194 | ||||||
chr21:42245231 | T | G | 1 | a0001c0001t0006g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.286+19317T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245231 | |||||||
chr21:42245390 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.286+19476G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245390 | |||||||
chr21:42245391 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+19477C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245391 | |||||||
chr21:42245523 | G | A | 1 | a0001c0001t0006g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+19609G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245523 | |||||||
chr21:42245668 | G | A | 1 | a0001c0002t0004g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19754G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245668 | |||||||
chr21:42245693 | A | C | 1 | a0001c0001t0026g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+19779A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245693 | |||||||
chr21:42245757 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.286+19843A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245757 | |||||||
chr21:42245773 | A | T | 2 | a0001c0001t0002g0306 a0001c0001t0028g0304 |
2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+19859A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245773 | |||||||
chr21:42245807 | T | C | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+19893T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245807 | |||||||
chr21:42245818 | T | TGGGGCAC others(29): Show |
139 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(136): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+19937_286+1997 others(40): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245818 | ||||||
chr21:42245818 | T | TGGGGCAC others(65): Show |
3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0007g0009 |
3 | HG01891.hp1 HG03540.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.286+19972_286+1997 others(76): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42245818 | ||||||
chr21:42245955 | T | C | 139 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(136): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.286+20041T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245955 | |||||||
chr21:42245960 | G | A | 106 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(103): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.286+20046G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42245960 | |||||||
chr21:42246064 | G | T | 2 | a0001c0002t0002g0080 a0001c0002t0016g0341 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.286+20150G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246064 | |||||||
chr21:42246498 | G | A | 2 | a0001c0001t0004g0088 a0001c0001t0004g0094 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.286+20584G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246498 | |||||||
chr21:42246529 | T | G | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+20615T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246529 | |||||||
chr21:42246578 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.286+20664A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246578 | |||||||
chr21:42246591 | G | A | 18 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
19 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+20677G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246591 | |||||||
chr21:42246753 | G | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0002g0075 others(1): Show |
4 | HG00438.hp2 NA18943.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+20839G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246753 | |||||||
chr21:42246972 | G | A | 104 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 others(101): Show |
108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.286+21058G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42246972 | |||||||
chr21:42247024 | AC | A | 6 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+21111delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247024 | |||||||
chr21:42247247 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.286+21333G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247247 | |||||||
chr21:42247268 | G | T | 2 | a0001c0001t0002g0306 a0001c0001t0028g0304 |
2 | HG01496.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286+21354G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247268 | |||||||
chr21:42247638 | C | T | 1 | a0001c0006t0004g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+21724C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247638 | |||||||
chr21:42247693 | G | T | 1 | a0001c0003t0003g0259 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.286+21779G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247693 | |||||||
chr21:42247746 | G | A | 19 | a0001c0001t0001g0091 a0001c0001t0001g0155 a0001c0001t0001g0278 others(16): Show |
20 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.286+21832G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247746 | |||||||
chr21:42247755 | C | A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0278 a0001c0001t0001g0326 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+21841C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247755 | |||||||
chr21:42247789 | G | A | 1 | a0001c0001t0012g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+21875G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247789 | |||||||
chr21:42247851 | G | A | 6 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+21937G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247851 | |||||||
chr21:42247880 | C | T | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286+21966C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247880 | |||||||
chr21:42247881 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.286+21967G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247881 | |||||||
chr21:42247908 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0015g0285 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.286+21994G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247908 | |||||||
chr21:42247944 | G | A | 5 | a0001c0001t0004g0169 a0001c0001t0004g0182 a0001c0001t0004g0311 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+22030G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247944 | |||||||
chr21:42247953 | C | T | 2 | a0001c0001t0002g0338 a0001c0001t0002g0339 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+22039C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42247953 | |||||||
chr21:42248063 | G | A | 1 | a0001c0001t0011g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.286+22149G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248063 | |||||||
chr21:42248087 | C | T | 1 | a0001c0001t0028g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+22173C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248087 | |||||||
chr21:42248104 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.286+22190G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248104 | |||||||
chr21:42248163 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0015g0285 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.286+22249A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248163 | |||||||
chr21:42248200 | C | T | 47 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0142 others(44): Show |
49 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.286+22286C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248200 | |||||||
chr21:42248252 | T | C | 1 | a0001c0001t0028g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286+22338T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248252 | |||||||
chr21:42248412 | G | A | 49 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0142 others(46): Show |
51 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.286+22498G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248412 | |||||||
chr21:42248468 | G | T | 1 | a0001c0001t0021g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.286+22554G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248468 | |||||||
chr21:42248616 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0016g0341 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.287-22454G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248616 | |||||||
chr21:42248747 | T | TA | 30 | a0001c0001t0001g0093 a0001c0001t0001g0142 a0001c0001t0001g0155 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-22312dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248747 | ||||||
chr21:42248806 | C | G | 10 | a0001c0001t0001g0253 a0001c0001t0002g0092 a0001c0001t0002g0251 others(7): Show |
10 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-22264C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248806 | |||||||
chr21:42248814 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-22256G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42248814 | |||||||
chr21:42248902 | C | CA | 46 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0098 others(43): Show |
47 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-22150dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | ||||||
chr21:42248902 | C | CAA | 84 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0133 others(81): Show |
87 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.287-22151_287-2215 others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | ||||||
chr21:42248902 | C | CAAA | 10 | a0001c0001t0002g0230 a0001c0001t0002g0286 a0001c0001t0002g0288 others(7): Show |
10 | HG00544.hp1 HG00639.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-22152_287-2215 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | ||||||
chr21:42248902 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-22159_287-2215 others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42248902 | ||||||
chr21:42249006 | A | G | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-22064A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249006 | |||||||
chr21:42249118 | G | C | 23 | a0001c0001t0001g0284 a0001c0001t0001g0314 a0001c0001t0001g0325 others(20): Show |
24 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-21952G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249118 | |||||||
chr21:42249259 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.287-21811C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249259 | |||||||
chr21:42249323 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.287-21747A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249323 | |||||||
chr21:42249339 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-21731A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249339 | |||||||
chr21:42249410 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-21660C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249410 | |||||||
chr21:42249500 | T | G | 16 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0253 others(13): Show |
16 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.287-21570T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249500 | |||||||
chr21:42249576 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0297 a0001c0001t0003g0300 |
3 | HG04199.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.287-21494G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249576 | |||||||
chr21:42249732 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-21338G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249732 | |||||||
chr21:42249762 | T | C | 23 | a0001c0001t0001g0284 a0001c0001t0001g0314 a0001c0001t0001g0325 others(20): Show |
24 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-21308T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249762 | |||||||
chr21:42249928 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.287-21142C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249928 | |||||||
chr21:42249937 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0024g0103 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.287-21133G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42249937 | |||||||
chr21:42250088 | T | G | 2 | a0001c0001t0001g0332 a0001c0001t0009g0331 |
2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.287-20982T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250088 | |||||||
chr21:42250212 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0002g0162 a0001c0001t0002g0164 others(3): Show |
6 | HG00408.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-20858C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250212 | |||||||
chr21:42250215 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.287-20855G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250215 | |||||||
chr21:42250265 | G | A | 8 | a0001c0001t0004g0169 a0001c0001t0004g0182 a0001c0001t0004g0311 others(5): Show |
8 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-20805G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250265 | |||||||
chr21:42250547 | C | G | 106 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0093 others(103): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.287-20523C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250547 | |||||||
chr21:42250735 | T | C | 5 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(2): Show |
5 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-20335T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250735 | |||||||
chr21:42250796 | C | T | 4 | a0001c0001t0002g0286 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-20274C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250796 | |||||||
chr21:42250886 | G | A | 1 | a0001c0001t0009g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-20184G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42250886 | |||||||
chr21:42251010 | G | C | 5 | a0001c0001t0002g0251 a0001c0001t0002g0254 a0001c0001t0002g0302 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-20060G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251010 | |||||||
chr21:42251050 | A | AG | 307 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(304): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.287-20020_287-2001 others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251050 | |||||||
chr21:42251061 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-20009A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251061 | |||||||
chr21:42251084 | C | T | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-19986C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251084 | |||||||
chr21:42251110 | C | T | 3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 |
3 | HG01099.hp2 HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.287-19960C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251110 | |||||||
chr21:42251290 | C | T | 1 | a0001c0001t0003g0163 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.287-19780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251290 | |||||||
chr21:42251291 | G | A | 1 | a0001c0007t0016g0345 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.287-19779G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251291 | |||||||
chr21:42251338 | G | A | 2 | a0001c0001t0003g0308 a0001c0001t0004g0309 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.287-19732G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251338 | |||||||
chr21:42251523 | C | G | 163 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0098 others(160): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.287-19547C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251523 | |||||||
chr21:42251543 | T | TGAG | 165 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0098 others(162): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.287-19525_287-1952 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42251543 | ||||||
chr21:42251660 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287-19410G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251660 | |||||||
chr21:42251701 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-19369C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251701 | |||||||
chr21:42251907 | G | C | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.287-19163G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251907 | |||||||
chr21:42251998 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.287-19072C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42251998 | |||||||
chr21:42252103 | C | T | 2 | a0001c0001t0003g0107 a0001c0001t0003g0108 |
2 | NA18939.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.287-18967C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252103 | |||||||
chr21:42252104 | G | A | 10 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0174 others(7): Show |
11 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-18966G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252104 | |||||||
chr21:42252422 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-18648G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252422 | |||||||
chr21:42252424 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-18646C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252424 | |||||||
chr21:42252425 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.287-18645G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252425 | |||||||
chr21:42252527 | T | A | 33 | a0001c0001t0001g0124 a0001c0001t0002g0162 a0001c0001t0002g0188 others(30): Show |
34 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-18543T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252527 | |||||||
chr21:42252528 | C | A | 33 | a0001c0001t0001g0124 a0001c0001t0002g0162 a0001c0001t0002g0188 others(30): Show |
34 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-18542C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252528 | |||||||
chr21:42252551 | C | A | 1 | a0001c0001t0006g0030 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-18519C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252551 | |||||||
chr21:42252703 | C | T | 5 | a0001c0001t0001g0253 a0001c0001t0004g0182 a0001c0001t0004g0268 others(2): Show |
5 | HG00738.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-18367C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252703 | |||||||
chr21:42252783 | C | T | 3 | a0001c0001t0002g0173 a0001c0001t0002g0233 a0001c0001t0003g0232 |
3 | HG00558.hp2 NA18942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.287-18287C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252783 | |||||||
chr21:42252839 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-18231G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252839 | |||||||
chr21:42252859 | C | G | 1 | a0001c0001t0005g0026 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.287-18211C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42252859 | |||||||
chr21:42253003 | G | C | 10 | a0001c0001t0001g0260 a0001c0001t0002g0112 a0001c0001t0002g0146 others(7): Show |
10 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-18067G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253003 | |||||||
chr21:42253021 | C | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0335 a0001c0002t0002g0270 |
3 | HG02622.hp1 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.287-18049C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253021 | |||||||
chr21:42253026 | C | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0222 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-18044C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253026 | |||||||
chr21:42253038 | G | A | 2 | a0001c0001t0004g0088 a0001c0001t0004g0094 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-18032G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253038 | |||||||
chr21:42253073 | C | T | 11 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0222 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-17997C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253073 | |||||||
chr21:42253265 | A | G | 11 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0222 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-17805A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253265 | |||||||
chr21:42253367 | G | C | 32 | a0001c0001t0001g0124 a0001c0001t0002g0162 a0001c0001t0002g0188 others(29): Show |
33 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.287-17703G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253367 | |||||||
chr21:42253557 | C | T | 4 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0006t0001g0008 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-17513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253557 | |||||||
chr21:42253568 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.287-17502C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253568 | |||||||
chr21:42253801 | G | GGAGGTCG others(1): Show |
6 | a0001c0001t0001g0165 a0001c0001t0002g0164 a0001c0001t0002g0230 others(3): Show |
6 | HG00408.hp2 HG00544.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-17267_287-1726 others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42253801 | ||||||
chr21:42253931 | C | G | 1 | a0001c0001t0009g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-17139C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42253931 | |||||||
chr21:42254012 | G | C | 224 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.287-17058G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254012 | |||||||
chr21:42254111 | A | G | 78 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(75): Show |
80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16959A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254111 | |||||||
chr21:42254118 | A | G | 78 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(75): Show |
80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254118 | |||||||
chr21:42254145 | C | G | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.287-16925C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254145 | |||||||
chr21:42254153 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-16917C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254153 | |||||||
chr21:42254289 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0004g0269 a0001c0001t0029g0262 |
3 | HG02451.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287-16781C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254289 | |||||||
chr21:42254481 | A | T | 2 | a0001c0001t0002g0162 a0001c0001t0005g0016 |
2 | NA18969.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.287-16589A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254481 | |||||||
chr21:42254574 | T | C | 76 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(73): Show |
78 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.287-16496T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254574 | |||||||
chr21:42254597 | G | A | 1 | a0001c0001t0006g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-16473G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254597 | |||||||
chr21:42254609 | G | A | 2 | a0001c0001t0009g0087 a0001c0001t0030g0310 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-16461G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254609 | |||||||
chr21:42254632 | G | A | 1 | a0001c0001t0006g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.287-16438G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254632 | |||||||
chr21:42254726 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-16344G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254726 | |||||||
chr21:42254749 | G | A | 78 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(75): Show |
80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.287-16321G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254749 | |||||||
chr21:42254760 | G | C | 1 | a0001c0001t0012g0305 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.287-16310G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254760 | |||||||
chr21:42254847 | C | T | 1 | a0001c0001t0004g0266 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.287-16223C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254847 | |||||||
chr21:42254872 | G | A | 44 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0001c0001t0002g0162 others(41): Show |
46 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-16198G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42254872 | |||||||
chr21:42255113 | C | T | 4 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0006t0001g0008 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15957C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255113 | |||||||
chr21:42255184 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0253 a0001c0001t0003g0111 others(2): Show |
5 | HG00738.hp2 HG02735.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15886C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255184 | |||||||
chr21:42255238 | C | T | 47 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0001c0001t0001g0271 others(44): Show |
50 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-15832C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255238 | |||||||
chr21:42255255 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.287-15815G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255255 | |||||||
chr21:42255324 | G | T | 4 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0006t0001g0008 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15746G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255324 | |||||||
chr21:42255393 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-15677C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255393 | |||||||
chr21:42255482 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.287-15588A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255482 | |||||||
chr21:42255500 | G | T | 4 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0006t0001g0008 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-15570G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255500 | |||||||
chr21:42255563 | C | T | 1 | a0001c0003t0005g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.287-15507C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255563 | |||||||
chr21:42255571 | T | C | 3 | a0001c0001t0009g0275 a0001c0002t0002g0080 a0001c0002t0004g0274 |
3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-15499T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255571 | |||||||
chr21:42255584 | A | G | 168 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(165): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.287-15486A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255584 | |||||||
chr21:42255661 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-15409T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255661 | |||||||
chr21:42255724 | T | C | 3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 |
3 | HG01099.hp2 HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.287-15346T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255724 | |||||||
chr21:42255741 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.287-15329T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255741 | |||||||
chr21:42255777 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0159 |
2 | HG02027.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.287-15293G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255777 | |||||||
chr21:42255830 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-15240C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255830 | |||||||
chr21:42255918 | T | G | 1 | a0001c0001t0006g0051 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-15152T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42255918 | |||||||
chr21:42256258 | C | T | 2 | a0001c0006t0001g0008 a0001c0006t0004g0319 |
3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-14812C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256258 | |||||||
chr21:42256277 | G | A | 32 | a0001c0001t0001g0099 a0001c0001t0001g0142 a0001c0001t0001g0315 others(29): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.287-14793G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256277 | |||||||
chr21:42256436 | T | C | 1 | a0001c0001t0022g0024 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.287-14634T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256436 | |||||||
chr21:42256476 | A | T | 34 | a0001c0001t0001g0124 a0001c0001t0002g0162 a0001c0001t0002g0188 others(31): Show |
35 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-14594A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256476 | |||||||
chr21:42256724 | G | A | 1 | a0001c0001t0006g0035 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.287-14346G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42256724 | |||||||
chr21:42257008 | C | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-14062C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257008 | |||||||
chr21:42257164 | G | A | 1 | a0001c0001t0007g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.287-13906G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257164 | |||||||
chr21:42257257 | G | A | 2 | a0001c0001t0009g0087 a0001c0001t0030g0310 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-13813G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257257 | |||||||
chr21:42257330 | G | C | 6 | a0001c0001t0001g0253 a0001c0001t0002g0134 a0001c0001t0002g0137 others(3): Show |
6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13740G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257330 | |||||||
chr21:42257355 | C | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0150 |
2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.287-13715C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257355 | |||||||
chr21:42257370 | A | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-13700A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257370 | |||||||
chr21:42257557 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0003g0090 a0001c0002t0002g0096 |
3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-13513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257557 | |||||||
chr21:42257563 | G | A | 2 | a0001c0001t0003g0300 a0002c0009t0003g0258 |
2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.287-13507G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257563 | |||||||
chr21:42257661 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-13409T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257661 | |||||||
chr21:42257721 | C | A | 212 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.287-13349C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257721 | |||||||
chr21:42257813 | G | T | 1 | a0001c0001t0009g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-13257G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257813 | |||||||
chr21:42257899 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.287-13171C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257899 | |||||||
chr21:42257932 | C | T | 6 | a0001c0001t0001g0333 a0001c0001t0004g0104 a0001c0001t0004g0105 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13138C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257932 | |||||||
chr21:42257955 | TCCATCCC others(189): Show |
T | 3 | a0001c0001t0001g0263 a0001c0001t0004g0265 a0001c0001t0004g0266 |
3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-13114_287-1291 others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257955 | |||||||
chr21:42257956 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-13114C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257956 | |||||||
chr21:42257956 | CCATCCCT others(189): Show |
C | 170 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(167): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.287-13058_287-1286 others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42257956 | ||||||
chr21:42257989 | C | T | 5 | a0001c0001t0001g0271 a0001c0001t0001g0326 a0001c0001t0012g0313 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13081C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42257989 | |||||||
chr21:42258214 | C | T | 2 | a0001c0006t0001g0008 a0001c0006t0004g0319 |
3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-12856C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258214 | |||||||
chr21:42258440 | A | G | 140 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(137): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.287-12630A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258440 | |||||||
chr21:42258680 | A | G | 1 | a0004c0013t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.287-12390A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258680 | |||||||
chr21:42258698 | C | T | 66 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-12372C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258698 | |||||||
chr21:42258753 | G | A | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-12317G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258753 | |||||||
chr21:42258934 | G | A | 29 | a0001c0001t0001g0099 a0001c0001t0001g0142 a0001c0001t0001g0315 others(26): Show |
29 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.287-12136G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258934 | |||||||
chr21:42258997 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-12073A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42258997 | |||||||
chr21:42259013 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-12057C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259013 | |||||||
chr21:42259328 | T | C | 69 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(66): Show |
71 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-11742T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259328 | |||||||
chr21:42259403 | C | T | 67 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(64): Show |
69 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-11667C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259403 | |||||||
chr21:42259444 | C | T | 69 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(66): Show |
71 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-11626C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259444 | |||||||
chr21:42259523 | G | A | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-11547G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259523 | |||||||
chr21:42259534 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11536G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259534 | |||||||
chr21:42259642 | A | G | 4 | a0001c0001t0001g0326 a0001c0001t0012g0313 a0001c0001t0015g0285 others(1): Show |
5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-11428A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259642 | |||||||
chr21:42259752 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11318G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259752 | |||||||
chr21:42259960 | C | G | 5 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(2): Show |
6 | HG01099.hp2 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-11110C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259960 | |||||||
chr21:42259996 | CGGCATCC others(8): Show |
C | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11072_287-1105 others(19): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42259996 | ||||||
chr21:42259997 | G | A | 6 | a0001c0001t0001g0336 a0001c0001t0004g0269 a0001c0001t0009g0275 others(3): Show |
6 | HG02109.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-11073G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42259997 | |||||||
chr21:42260034 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-11036C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260034 | |||||||
chr21:42260058 | A | C | 1 | a0001c0001t0003g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.287-11012A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260058 | |||||||
chr21:42260222 | T | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-10848T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260222 | |||||||
chr21:42260288 | C | T | 5 | a0001c0001t0001g0326 a0001c0001t0001g0336 a0001c0001t0012g0313 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-10782C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260288 | |||||||
chr21:42260305 | C | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-10765C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260305 | |||||||
chr21:42260310 | C | G | 10 | a0001c0001t0001g0253 a0001c0001t0001g0284 a0001c0001t0002g0134 others(7): Show |
10 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-10760C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260310 | |||||||
chr21:42260354 | C | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(18): Show |
21 | HG01167.hp1 HG01884.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-10716C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260354 | |||||||
chr21:42260569 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.287-10501C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260569 | |||||||
chr21:42260608 | A | T | 1 | a0001c0001t0001g0325 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.287-10462A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260608 | |||||||
chr21:42260700 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-10370A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260700 | |||||||
chr21:42260829 | C | CT | 12 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(9): Show |
12 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-10230dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42260829 | ||||||
chr21:42260967 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10103G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260967 | |||||||
chr21:42260968 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10102C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260968 | |||||||
chr21:42260969 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10101C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260969 | |||||||
chr21:42260970 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-10100A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42260970 | |||||||
chr21:42261120 | C | T | 7 | a0001c0001t0001g0326 a0001c0001t0001g0336 a0001c0001t0004g0088 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-9950C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261120 | |||||||
chr21:42261195 | C | A | 1 | a0001c0001t0012g0305 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.287-9875C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261195 | |||||||
chr21:42261213 | CT | C | 8 | a0001c0001t0004g0269 a0001c0001t0009g0087 a0001c0001t0009g0275 others(5): Show |
9 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-9856delT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261213 | |||||||
chr21:42261215 | C | G | 8 | a0001c0001t0004g0269 a0001c0001t0009g0087 a0001c0001t0009g0275 others(5): Show |
9 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-9855C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261215 | |||||||
chr21:42261287 | A | C | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-9783A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261287 | |||||||
chr21:42261373 | C | T | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.287-9697C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261373 | |||||||
chr21:42261527 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-9543G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261527 | |||||||
chr21:42261588 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-9482T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261588 | |||||||
chr21:42261589 | C | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-9481C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261589 | |||||||
chr21:42261793 | G | A | 4 | a0001c0001t0009g0087 a0001c0001t0009g0320 a0001c0001t0009g0321 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9277G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261793 | |||||||
chr21:42261840 | T | C | 2 | a0001c0001t0001g0332 a0001c0001t0009g0331 |
2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.287-9230T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261840 | |||||||
chr21:42261841 | T | A | 1 | a0001c0001t0003g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.287-9229T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261841 | |||||||
chr21:42261846 | A | G | 31 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0002g0162 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-9224A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261846 | |||||||
chr21:42261973 | G | A | 8 | a0001c0001t0001g0326 a0001c0001t0001g0336 a0001c0001t0009g0275 others(5): Show |
9 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-9097G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42261973 | |||||||
chr21:42262026 | C | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9044C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262026 | |||||||
chr21:42262067 | G | A | 66 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-9003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262067 | |||||||
chr21:42262099 | G | A | 2 | a0001c0006t0001g0008 a0001c0006t0004g0319 |
3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-8971G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262099 | |||||||
chr21:42262124 | G | C | 1 | a0001c0001t0006g0052 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.287-8946G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262124 | |||||||
chr21:42262134 | C | T | 142 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(139): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.287-8936C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262134 | |||||||
chr21:42262217 | G | C | 2 | a0001c0001t0003g0149 a0001c0001t0007g0009 |
2 | NA18964.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.287-8853G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262217 | |||||||
chr21:42262255 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-8815G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262255 | |||||||
chr21:42262260 | G | C | 66 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0142 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-8810G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262260 | |||||||
chr21:42262284 | G | A | 137 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(134): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.287-8786G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262284 | |||||||
chr21:42262291 | ATTC | A | 4 | a0001c0001t0002g0293 a0001c0001t0006g0049 a0001c0001t0006g0051 others(1): Show |
4 | HG01433.hp1 HG02083.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-8773_287-8771d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42262291 | ||||||
chr21:42262420 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0004g0265 a0001c0001t0004g0266 |
3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-8650C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262420 | |||||||
chr21:42262429 | C | T | 31 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0002g0162 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-8641C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262429 | |||||||
chr21:42262576 | G | A | 141 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(138): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.287-8494G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262576 | |||||||
chr21:42262600 | A | G | 3 | a0001c0001t0009g0275 a0001c0002t0002g0080 a0001c0002t0004g0274 |
3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-8470A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262600 | |||||||
chr21:42262601 | A | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-8469A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262601 | |||||||
chr21:42262691 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0004g0265 a0001c0001t0004g0266 |
3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-8379C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262691 | |||||||
chr21:42262698 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.287-8372A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262698 | |||||||
chr21:42262757 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-8313C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262757 | |||||||
chr21:42262810 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-8260T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262810 | |||||||
chr21:42262828 | A | G | 156 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(153): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.287-8242A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262828 | |||||||
chr21:42262849 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.287-8221G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262849 | |||||||
chr21:42262942 | C | T | 3 | a0001c0003t0003g0211 a0001c0003t0005g0054 a0001c0003t0007g0056 |
3 | NA18952.hp1 NA18981.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.287-8128C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262942 | |||||||
chr21:42262943 | A | G | 138 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.287-8127A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42262943 | |||||||
chr21:42263151 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-7919C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263151 | |||||||
chr21:42263290 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0014g0063 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-7780C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263290 | |||||||
chr21:42263312 | C | T | 1 | a0001c0001t0009g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-7758C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263312 | |||||||
chr21:42263412 | C | T | 3 | a0001c0001t0002g0338 a0001c0001t0002g0339 a0001c0012t0004g0276 |
3 | HG01168.hp1 HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-7658C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263412 | |||||||
chr21:42263493 | C | T | 1 | a0001c0002t0002g0329 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.287-7577C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263493 | |||||||
chr21:42263533 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.287-7537C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263533 | |||||||
chr21:42263569 | T | C | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-7501T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263569 | |||||||
chr21:42263587 | C | T | 2 | a0001c0001t0004g0283 a0001c0001t0004g0334 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.287-7483C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263587 | |||||||
chr21:42263631 | C | T | 6 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0251 others(3): Show |
6 | HG01099.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-7439C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263631 | |||||||
chr21:42263742 | T | C | 2 | a0001c0001t0006g0064 a0001c0001t0014g0065 |
2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.287-7328T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263742 | |||||||
chr21:42263759 | G | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(18): Show |
21 | HG01167.hp1 HG01884.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-7311G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263759 | |||||||
chr21:42263859 | C | T | 39 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(36): Show |
40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-7211C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263859 | |||||||
chr21:42263870 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.287-7200C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263870 | |||||||
chr21:42263871 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0004g0265 a0001c0001t0004g0266 |
3 | HG01261.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-7199G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263871 | |||||||
chr21:42263991 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-7079G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42263991 | |||||||
chr21:42264094 | G | A | 2 | a0001c0001t0004g0088 a0001c0001t0004g0094 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-6976G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264094 | |||||||
chr21:42264186 | G | A | 2 | a0001c0006t0001g0008 a0001c0006t0004g0319 |
3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-6884G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264186 | |||||||
chr21:42264189 | A | G | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6881A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264189 | |||||||
chr21:42264211 | C | T | 39 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0001t0001g0165 others(36): Show |
39 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.287-6859C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264211 | |||||||
chr21:42264305 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6765G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264305 | |||||||
chr21:42264346 | G | A | 137 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(134): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.287-6724G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264346 | |||||||
chr21:42264438 | C | T | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-6632C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264438 | |||||||
chr21:42264439 | G | A | 142 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(139): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.287-6631G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264439 | |||||||
chr21:42264442 | A | C | 1 | a0001c0001t0005g0069 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.287-6628A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264442 | |||||||
chr21:42264469 | T | A | 1 | a0002c0009t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.287-6601T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264469 | |||||||
chr21:42264475 | A | G | 223 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.287-6595A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264475 | |||||||
chr21:42264489 | CCATCCAT others(1): Show |
C | 142 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(139): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.287-6557_287-6550d others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42264489 | ||||||
chr21:42264557 | C | T | 1 | a0001c0001t0006g0030 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-6513C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264557 | |||||||
chr21:42264558 | G | A | 6 | a0001c0001t0001g0253 a0001c0001t0002g0134 a0001c0001t0002g0137 others(3): Show |
6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-6512G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264558 | |||||||
chr21:42264582 | CAGG | C | 39 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(36): Show |
40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6487_287-6485d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264582 | |||||||
chr21:42264586 | G | C | 39 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(36): Show |
40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6484G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264586 | |||||||
chr21:42264681 | G | A | 142 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(139): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.287-6389G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264681 | |||||||
chr21:42264800 | C | T | 1 | a0001c0001t0006g0018 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.287-6270C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264800 | |||||||
chr21:42264931 | C | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-6139C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264931 | |||||||
chr21:42264952 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-6118C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42264952 | |||||||
chr21:42265012 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.287-6058G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265012 | |||||||
chr21:42265013 | A | G | 185 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(182): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.287-6057A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265013 | |||||||
chr21:42265269 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-5801C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265269 | |||||||
chr21:42265494 | G | A | 14 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0336 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.287-5576G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265494 | |||||||
chr21:42265527 | C | T | 16 | a0001c0001t0001g0145 a0001c0001t0001g0159 a0001c0001t0001g0260 others(13): Show |
17 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.287-5543C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265527 | |||||||
chr21:42265554 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-5516C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265554 | |||||||
chr21:42265642 | C | T | 25 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-5428C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265642 | |||||||
chr21:42265643 | G | A | 139 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(136): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.287-5427G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265643 | |||||||
chr21:42265644 | G | A | 182 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(179): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.287-5426G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265644 | |||||||
chr21:42265655 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.287-5415G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265655 | |||||||
chr21:42265698 | G | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-5372G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265698 | |||||||
chr21:42265764 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.287-5306G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265764 | |||||||
chr21:42265798 | G | A | 6 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0335 others(3): Show |
6 | HG01167.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5272G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265798 | |||||||
chr21:42265838 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-5232C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265838 | |||||||
chr21:42265875 | C | T | 141 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(138): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.287-5195C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265875 | |||||||
chr21:42265897 | C | T | 1 | a0001c0001t0004g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-5173C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42265897 | |||||||
chr21:42266118 | A | G | 2 | a0001c0001t0009g0087 a0001c0001t0030g0310 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.287-4952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266118 | |||||||
chr21:42266171 | C | T | 4 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0254 others(1): Show |
4 | HG01099.hp2 HG01175.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-4899C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266171 | |||||||
chr21:42266172 | G | A | 4 | a0001c0001t0004g0269 a0001c0001t0009g0087 a0001c0001t0014g0063 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-4898G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266172 | |||||||
chr21:42266216 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0014g0063 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-4854G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266216 | |||||||
chr21:42266258 | G | A | 3 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-4812G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266258 | |||||||
chr21:42266261 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-4809A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266261 | |||||||
chr21:42266309 | T | TAAATA | 13 | a0001c0001t0001g0085 a0001c0001t0001g0099 a0001c0001t0001g0115 others(10): Show |
13 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-4737_287-4733d others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42266309 | ||||||
chr21:42266309 | T | TAAATAAA others(3): Show |
18 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0335 others(15): Show |
18 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-4742_287-4733d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42266309 | ||||||
chr21:42266328 | T | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-4742T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266328 | |||||||
chr21:42266333 | T | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-4737T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266333 | |||||||
chr21:42266373 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.287-4697A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266373 | |||||||
chr21:42266439 | G | T | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.287-4631G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266439 | |||||||
chr21:42266572 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-4498C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266572 | |||||||
chr21:42266601 | A | G | 1 | a0001c0001t0030g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-4469A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266601 | |||||||
chr21:42266660 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287-4410G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266660 | |||||||
chr21:42266731 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.287-4339A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266731 | |||||||
chr21:42266756 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0009g0087 a0001c0001t0030g0310 |
3 | HG02145.hp1 HG02559.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.287-4314G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266756 | |||||||
chr21:42266757 | T | C | 1 | a0001c0001t0006g0051 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-4313T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266757 | |||||||
chr21:42266882 | T | C | 220 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.287-4188T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266882 | |||||||
chr21:42266924 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-4146C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42266924 | |||||||
chr21:42267032 | G | T | 40 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(37): Show |
42 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-4038G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267032 | |||||||
chr21:42267212 | C | T | 25 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-3858C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267212 | |||||||
chr21:42267244 | C | T | 138 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.287-3826C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267244 | |||||||
chr21:42267276 | T | C | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-3794T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267276 | |||||||
chr21:42267297 | G | C | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0234 |
3 | HG02258.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.287-3773G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267297 | |||||||
chr21:42267332 | C | T | 7 | a0001c0001t0001g0253 a0001c0001t0002g0134 a0001c0001t0002g0137 others(4): Show |
7 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-3738C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267332 | |||||||
chr21:42267343 | CTGGGTTC others(15): Show |
C | 3 | a0001c0001t0001g0091 a0001c0001t0003g0090 a0001c0002t0002g0096 |
3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-3707_287-3686d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267343 | ||||||
chr21:42267437 | G | GTGGTCCG others(15): Show |
3 | a0001c0001t0009g0275 a0001c0002t0002g0080 a0001c0002t0004g0274 |
3 | HG02109.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-3627_287-3606d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267437 | ||||||
chr21:42267443 | CGAGTTCT others(59): Show |
C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0263 a0001c0001t0004g0265 others(1): Show |
4 | HG01261.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3586_287-3521d others(68): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267443 | ||||||
chr21:42267457 | G | A | 138 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.287-3613G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267457 | |||||||
chr21:42267466 | G | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-3604G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267466 | |||||||
chr21:42267501 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0205 a0001c0001t0003g0074 others(1): Show |
4 | HG01243.hp1 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3569G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267501 | |||||||
chr21:42267507 | T | A | 3 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-3563T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267507 | |||||||
chr21:42267528 | G | C | 4 | a0001c0001t0001g0336 a0001c0001t0012g0313 a0001c0001t0015g0285 others(1): Show |
5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-3542G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267528 | |||||||
chr21:42267537 | C | T | 134 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(131): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.287-3533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267537 | |||||||
chr21:42267635 | G | C | 220 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.287-3435G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267635 | |||||||
chr21:42267637 | G | C | 220 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.287-3433G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267637 | |||||||
chr21:42267833 | C | G | 1 | a0001c0001t0002g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287-3237C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267833 | |||||||
chr21:42267859 | T | A | 1 | a0001c0001t0007g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.287-3211T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267859 | |||||||
chr21:42267866 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-3204C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267866 | |||||||
chr21:42267866 | CTGGTCTG others(15): Show |
C | 34 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0002g0162 others(31): Show |
35 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-3142_287-3121d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267866 | ||||||
chr21:42267890 | G | C | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287-3180G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267890 | |||||||
chr21:42267903 | T | C | 4 | a0001c0001t0001g0336 a0001c0001t0012g0313 a0001c0001t0015g0285 others(1): Show |
5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-3167T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42267903 | |||||||
chr21:42267920 | TTCTGTCT others(19): Show |
T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0263 a0001c0001t0004g0265 others(1): Show |
4 | HG01261.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-3146_287-3121d others(28): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42267920 | ||||||
chr21:42268108 | A | G | 1 | a0001c0001t0008g0343 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-2962A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268108 | |||||||
chr21:42268362 | G | GGT | 6 | a0001c0001t0001g0159 a0001c0001t0001g0200 a0001c0001t0003g0108 others(3): Show |
6 | HG01975.hp1 NA18943.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2682_287-2681d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268362 | G | GGTGT | 15 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0205 others(12): Show |
16 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-2684_287-2681d others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268362 | G | GGTGTGT | 16 | a0001c0001t0001g0332 a0001c0001t0002g0181 a0001c0001t0004g0004 others(13): Show |
17 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.287-2686_287-2681d others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268362 | G | GGTGTGTG others(1): Show |
73 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0126 others(70): Show |
73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-2688_287-2681d others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268362 | G | GGTGTGTG others(3): Show |
14 | a0001c0001t0001g0098 a0001c0001t0001g0212 a0001c0001t0002g0113 others(11): Show |
14 | HG00408.hp1 HG00558.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-2690_287-2681d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268362 | G | GGTGTGTG others(5): Show |
4 | a0001c0001t0001g0290 a0001c0001t0004g0182 a0001c0001t0009g0087 others(1): Show |
4 | HG00280.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2692_287-2681d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268362 | ||||||
chr21:42268381 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0091 a0001c0001t0003g0090 a0001c0002t0002g0096 |
3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-2682_287-2681i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268381 | ||||||
chr21:42268386 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.287-2684T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268386 | |||||||
chr21:42268386 | T | TGCGC | 19 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0335 others(16): Show |
19 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-2683_287-2682i others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268386 | ||||||
chr21:42268388 | T | C | 21 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(18): Show |
21 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-2682T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268388 | |||||||
chr21:42268388 | T | TGCGCGC | 4 | a0001c0001t0003g0153 a0001c0001t0004g0337 a0001c0002t0002g0282 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2675_287-2670d others(8): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGCG others(1): Show |
9 | a0001c0001t0001g0333 a0001c0001t0001g0336 a0001c0001t0004g0104 others(6): Show |
10 | HG01891.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(1): Show |
7 | a0001c0001t0001g0078 a0001c0001t0001g0271 a0001c0001t0002g0183 others(4): Show |
7 | HG02683.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(10): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287-2681_287-2680i others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(3): Show |
25 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0002g0162 others(22): Show |
26 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0004g0269 a0001c0001t0014g0063 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-2681_287-2680i others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(5): Show |
13 | a0001c0001t0001g0142 a0001c0001t0001g0253 a0001c0001t0002g0134 others(10): Show |
14 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-2681_287-2680i others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(13): Show |
2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.287-2681_287-2680i others(22): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268388 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.287-2681_287-2680i others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42268388 | ||||||
chr21:42268390 | C | T | 18 | a0001c0001t0001g0085 a0001c0001t0001g0139 a0001c0001t0001g0205 others(15): Show |
19 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-2680C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268390 | |||||||
chr21:42268392 | C | T | 56 | a0001c0001t0001g0085 a0001c0001t0001g0124 a0001c0001t0001g0139 others(53): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.287-2678C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268392 | |||||||
chr21:42268395 | G | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-2675G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268395 | |||||||
chr21:42268397 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.287-2673G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268397 | |||||||
chr21:42268398 | C | T | 2 | a0001c0004t0003g0003 a0001c0004t0003g0076 |
3 | NA19003.hp2 NA19004.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.287-2672C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268398 | |||||||
chr21:42268405 | T | C | 27 | a0001c0001t0001g0099 a0001c0001t0001g0315 a0001c0001t0001g0325 others(24): Show |
27 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-2665T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268405 | |||||||
chr21:42268426 | A | G | 2 | a0001c0006t0001g0008 a0001c0006t0004g0319 |
3 | HG01070.hp2 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.287-2644A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268426 | |||||||
chr21:42268484 | G | C | 206 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(203): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.287-2586G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268484 | |||||||
chr21:42268602 | A | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-2468A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268602 | |||||||
chr21:42268679 | G | T | 1 | a0001c0001t0003g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-2391G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268679 | |||||||
chr21:42268719 | C | T | 3 | a0001c0001t0004g0311 a0001c0001t0009g0320 a0001c0001t0009g0321 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.287-2351C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268719 | |||||||
chr21:42268835 | C | G | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287-2235C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42268835 | |||||||
chr21:42269005 | G | T | 7 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0286 others(4): Show |
7 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-2065G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269005 | |||||||
chr21:42269065 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.287-2005G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269065 | |||||||
chr21:42269067 | C | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-2003C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269067 | |||||||
chr21:42269284 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-1786G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269284 | |||||||
chr21:42269381 | C | T | 96 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(93): Show |
99 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.287-1689C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269381 | |||||||
chr21:42269408 | C | A | 10 | a0001c0003t0001g0250 a0001c0003t0003g0211 a0001c0003t0003g0259 others(7): Show |
10 | HG00408.hp1 HG00558.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-1662C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269408 | |||||||
chr21:42269410 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.287-1660C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269410 | |||||||
chr21:42269493 | G | T | 2 | a0001c0007t0015g0346 a0001c0007t0016g0345 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-1577G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269493 | |||||||
chr21:42269583 | TC | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0338 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-1484delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42269583 | ||||||
chr21:42269616 | G | T | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.287-1454G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269616 | |||||||
chr21:42269647 | G | A | 1 | a0001c0001t0006g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-1423G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269647 | |||||||
chr21:42269703 | G | A | 1 | a0001c0001t0004g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-1367G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269703 | |||||||
chr21:42269740 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-1330T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269740 | |||||||
chr21:42269760 | A | G | 97 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(94): Show |
100 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.287-1310A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42269760 | |||||||
chr21:42270016 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0014g0063 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287-1054A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270016 | |||||||
chr21:42270259 | C | CA | 8 | a0001c0001t0002g0226 a0001c0001t0002g0267 a0001c0001t0002g0288 others(5): Show |
8 | HG01123.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-789dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270259 | C | CAAA | 7 | a0001c0001t0001g0156 a0001c0001t0001g0204 a0001c0001t0002g0225 others(4): Show |
7 | HG01070.hp1 HG01975.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-791_287-789dup others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270259 | C | CAAAA | 61 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.287-792_287-789dup others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270259 | C | CAAAAA | 31 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0315 others(28): Show |
31 | HG01106.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.287-793_287-789dup others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270259 | C | CAAAAAA | 8 | a0001c0001t0001g0336 a0001c0001t0002g0092 a0001c0001t0002g0277 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-794_287-789dup others(6): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270259 | CA | C | 94 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0091 others(91): Show |
97 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.287-789delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr21 | 42270259 | ||||||
chr21:42270309 | A | C | 1 | a0001c0001t0003g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-761A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270309 | |||||||
chr21:42270330 | T | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.287-740T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270330 | |||||||
chr21:42270528 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.287-542C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270528 | |||||||
chr21:42270748 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.287-322G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270748 | |||||||
chr21:42270768 | G | C | 1 | a0001c0001t0030g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-302G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270768 | |||||||
chr21:42270828 | T | G | 7 | a0001c0001t0001g0333 a0001c0001t0004g0269 a0001c0001t0009g0087 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-242T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270828 | |||||||
chr21:42270831 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.287-239A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270831 | |||||||
chr21:42270902 | A | G | 6 | a0001c0001t0001g0271 a0001c0001t0001g0326 a0001c0001t0001g0336 others(3): Show |
7 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-168A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270902 | |||||||
chr21:42270956 | A | G | 1 | a0001c0001t0012g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-114A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270956 | |||||||
chr21:42270984 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0006g0013 |
2 | NA18939.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.287-86C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42270984 | |||||||
chr21:42271029 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0336 a0001c0001t0012g0313 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-41A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 2/14 | chr21 | 42271029 | |||||||
chr21:42271212 | A | G | 1 | a0001c0001t0003g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.404+25A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271212 | |||||||
chr21:42271359 | G | C | 37 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0093 others(34): Show |
37 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.404+172G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271359 | |||||||
chr21:42271466 | T | TCAGGGAG others(16): Show |
4 | a0001c0001t0003g0308 a0001c0001t0009g0275 a0001c0001t0017g0007 others(1): Show |
5 | HG01109.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+281_404+303dup others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr21 | 42271466 | ||||||
chr21:42271656 | C | T | 2 | a0001c0001t0004g0088 a0001c0001t0004g0094 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.404+469C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271656 | |||||||
chr21:42271657 | G | A | 4 | a0001c0001t0001g0325 a0001c0001t0001g0336 a0001c0001t0015g0285 others(1): Show |
5 | HG01167.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+470G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271657 | |||||||
chr21:42271662 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.404+475A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271662 | |||||||
chr21:42271930 | G | A | 27 | a0001c0001t0002g0162 a0001c0001t0002g0181 a0001c0001t0002g0229 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.404+743G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271930 | |||||||
chr21:42271931 | T | C | 27 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0263 others(24): Show |
29 | HG01070.hp2 HG01071.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.404+744T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42271931 | |||||||
chr21:42272055 | T | C | 1 | a0001c0007t0016g0345 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.404+868T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272055 | |||||||
chr21:42272269 | T | A | 3 | a0001c0001t0002g0092 a0001c0001t0004g0088 a0001c0001t0004g0094 |
3 | HG01167.hp2 HG01169.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.405-1034T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272269 | |||||||
chr21:42272314 | T | C | 4 | a0001c0001t0001g0336 a0001c0001t0012g0313 a0001c0001t0015g0285 others(1): Show |
5 | HG02630.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-989T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272314 | |||||||
chr21:42272431 | A | G | 3 | a0001c0001t0001g0336 a0001c0001t0012g0313 a0001c0002t0004g0005 |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-872A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272431 | |||||||
chr21:42272442 | G | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.405-861G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272442 | |||||||
chr21:42272563 | G | A | 16 | a0001c0001t0001g0271 a0001c0001t0001g0326 a0001c0001t0001g0333 others(13): Show |
17 | HG01496.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-740G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272563 | |||||||
chr21:42272704 | G | C | 9 | a0001c0001t0001g0333 a0001c0001t0002g0277 a0001c0001t0004g0269 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-599G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272704 | |||||||
chr21:42272712 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.405-591G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272712 | |||||||
chr21:42272731 | T | C | 81 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(78): Show |
82 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.405-572T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272731 | |||||||
chr21:42272917 | C | T | 2 | a0001c0001t0009g0275 a0001c0002t0002g0143 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.405-386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272917 | |||||||
chr21:42272996 | C | G | 2 | a0001c0001t0009g0320 a0001c0001t0009g0321 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405-307C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42272996 | |||||||
chr21:42273140 | C | T | 2 | a0001c0001t0003g0125 a0001c0001t0003g0239 |
2 | HG01496.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.405-163C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273140 | |||||||
chr21:42273159 | G | T | 3 | a0001c0001t0001g0114 a0001c0001t0002g0116 a0001c0001t0005g0062 |
3 | HG02040.hp2 NA18944.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.405-144G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273159 | |||||||
chr21:42273218 | C | T | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.405-85C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 3/14 | chr21 | 42273218 | |||||||
chr21:42273454 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.537+19C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273454 | |||||||
chr21:42273474 | G | C | 108 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(105): Show |
109 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.537+39G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273474 | |||||||
chr21:42273583 | G | A | 53 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0253 others(50): Show |
53 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.537+148G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273583 | |||||||
chr21:42273631 | A | T | 5 | a0001c0001t0002g0173 a0001c0001t0002g0233 a0001c0001t0003g0232 others(2): Show |
5 | HG00558.hp2 HG01993.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+196A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273631 | |||||||
chr21:42273693 | A | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.537+258A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273693 | |||||||
chr21:42273707 | G | A | 1 | a0001c0001t0030g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.537+272G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273707 | |||||||
chr21:42273791 | T | G | 1 | a0004c0013t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.537+356T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273791 | |||||||
chr21:42273808 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0006g0030 |
2 | NA18942.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.537+373G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273808 | |||||||
chr21:42273927 | T | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.537+492T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42273927 | |||||||
chr21:42274021 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.537+586G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274021 | |||||||
chr21:42274023 | G | T | 1 | a0001c0003t0006g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.537+588G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274023 | |||||||
chr21:42274162 | C | T | 4 | a0001c0001t0001g0333 a0001c0001t0031g0079 a0001c0002t0002g0270 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+727C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274162 | |||||||
chr21:42274199 | A | T | 9 | a0001c0003t0001g0250 a0001c0003t0003g0211 a0001c0003t0005g0044 others(6): Show |
9 | HG00408.hp1 HG01975.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+764A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274199 | |||||||
chr21:42274291 | A | G | 15 | a0001c0001t0001g0333 a0001c0001t0002g0092 a0001c0001t0002g0277 others(12): Show |
16 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.537+856A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274291 | |||||||
chr21:42274297 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0003g0090 |
2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.537+862T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274297 | |||||||
chr21:42274326 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.537+891G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274326 | |||||||
chr21:42274393 | G | C | 13 | a0001c0001t0001g0333 a0001c0001t0002g0277 a0001c0001t0004g0269 others(10): Show |
14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.537+958G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274393 | |||||||
chr21:42274436 | G | A | 3 | a0001c0001t0002g0277 a0001c0001t0009g0087 a0001c0001t0030g0310 |
3 | HG02145.hp1 HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.537+1001G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274436 | |||||||
chr21:42274438 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0314 a0001c0001t0004g0266 |
3 | HG01261.hp2 HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.537+1003G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274438 | |||||||
chr21:42274475 | C | CT | 50 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0166 others(47): Show |
50 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.537+1056dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | ||||||
chr21:42274475 | C | CTT | 102 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(99): Show |
104 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+1055_537+1056d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | ||||||
chr21:42274475 | C | CTTT | 34 | a0001c0001t0001g0243 a0001c0001t0001g0315 a0001c0001t0001g0335 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+1054_537+1056d others(5): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274475 | ||||||
chr21:42274491 | T | G | 2 | a0001c0001t0010g0006 a0001c0001t0010g0301 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.537+1056T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274491 | |||||||
chr21:42274492 | G | T | 178 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.537+1057G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274492 | |||||||
chr21:42274560 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.537+1125C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274560 | |||||||
chr21:42274620 | G | A | 90 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.537+1185G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274620 | |||||||
chr21:42274635 | C | T | 9 | a0001c0001t0001g0271 a0001c0001t0001g0336 a0001c0001t0004g0104 others(6): Show |
10 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.537+1200C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274635 | |||||||
chr21:42274690 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0002g0303 |
2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.537+1255G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274690 | |||||||
chr21:42274715 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.537+1280T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274715 | |||||||
chr21:42274779 | ATT | A | 127 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+1354_537+1355d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42274779 | ||||||
chr21:42274870 | G | A | 25 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0335 others(22): Show |
25 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.537+1435G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42274870 | |||||||
chr21:42275030 | T | A | 101 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.537+1595T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275030 | |||||||
chr21:42275220 | T | C | 11 | a0001c0001t0001g0326 a0001c0001t0002g0277 a0001c0001t0002g0306 others(8): Show |
12 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.538-1675T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275220 | |||||||
chr21:42275351 | C | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.538-1544C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275351 | |||||||
chr21:42275378 | G | C | 101 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.538-1517G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275378 | |||||||
chr21:42275423 | G | A | 9 | a0001c0001t0002g0277 a0001c0001t0004g0269 a0001c0001t0006g0064 others(6): Show |
10 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.538-1472G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275423 | |||||||
chr21:42275636 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-1259T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275636 | |||||||
chr21:42275674 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.538-1221A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275674 | |||||||
chr21:42275729 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.538-1166C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275729 | |||||||
chr21:42275772 | C | T | 9 | a0001c0001t0002g0277 a0001c0001t0004g0269 a0001c0001t0006g0064 others(6): Show |
10 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.538-1123C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275772 | |||||||
chr21:42275815 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0014g0063 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.538-1080C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275815 | |||||||
chr21:42275862 | A | G | 2 | a0001c0001t0002g0277 a0001c0001t0009g0087 |
2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.538-1033A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42275862 | |||||||
chr21:42276042 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-853C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276042 | |||||||
chr21:42276122 | G | A | 1 | a0001c0001t0021g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.538-773G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276122 | |||||||
chr21:42276215 | C | A | 8 | a0001c0001t0001g0336 a0001c0001t0004g0104 a0001c0001t0004g0105 others(5): Show |
9 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-680C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276215 | |||||||
chr21:42276301 | G | C | 2 | a0001c0001t0001g0332 a0001c0001t0009g0331 |
2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.538-594G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276301 | |||||||
chr21:42276335 | C | G | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.538-560C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276335 | |||||||
chr21:42276424 | C | A | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.538-471C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276424 | |||||||
chr21:42276447 | C | T | 1 | a0001c0001t0004g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.538-448C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276447 | |||||||
chr21:42276682 | ATAGCTGC others(68): Show |
A | 9 | a0001c0001t0002g0277 a0001c0001t0004g0269 a0001c0001t0004g0337 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.538-199_538-125del others(75): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr21 | 42276682 | ||||||
chr21:42276692 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.538-203C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276692 | |||||||
chr21:42276707 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.538-188C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276707 | |||||||
chr21:42276723 | G | A | 27 | a0001c0001t0002g0162 a0001c0001t0002g0181 a0001c0001t0002g0229 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.538-172G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276723 | |||||||
chr21:42276840 | A | G | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0003g0118 |
3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.538-55A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276840 | |||||||
chr21:42276889 | C | T | 26 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0185 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.538-6C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 4/14 | chr21 | 42276889 | |||||||
chr21:42277008 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+63G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277008 | |||||||
chr21:42277070 | G | A | 10 | a0001c0001t0001g0271 a0001c0001t0001g0326 a0001c0001t0002g0306 others(7): Show |
11 | HG01109.hp2 HG01496.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+125G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277070 | |||||||
chr21:42277085 | A | G | 104 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(101): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.588+140A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277085 | |||||||
chr21:42277182 | G | C | 13 | a0001c0001t0001g0271 a0001c0001t0001g0326 a0001c0001t0002g0277 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+237G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277182 | |||||||
chr21:42277300 | A | G | 10 | a0001c0001t0002g0277 a0001c0001t0004g0269 a0001c0001t0004g0337 others(7): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+355A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277300 | |||||||
chr21:42277426 | A | G | 1 | a0001c0006t0004g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+481A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277426 | |||||||
chr21:42277468 | A | AT | 63 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0335 others(60): Show |
65 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.588+533dupT | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr21 | 42277468 | ||||||
chr21:42277963 | T | G | 55 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0278 others(52): Show |
56 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.588+1018T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277963 | |||||||
chr21:42277968 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+1023T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277968 | |||||||
chr21:42277997 | G | A | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.588+1052G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42277997 | |||||||
chr21:42278123 | A | T | 1 | a0001c0003t0005g0044 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.588+1178A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278123 | |||||||
chr21:42278137 | G | A | 1 | a0001c0006t0001g0008 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.588+1192G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278137 | |||||||
chr21:42278141 | G | A | 122 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0114 others(119): Show |
126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.588+1196G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278141 | |||||||
chr21:42278145 | A | C | 156 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0114 others(153): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.588+1200A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278145 | |||||||
chr21:42278183 | G | C | 5 | a0001c0001t0002g0277 a0001c0001t0004g0337 a0001c0001t0006g0066 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1238G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278183 | |||||||
chr21:42278293 | C | A | 2 | a0001c0001t0004g0264 a0001c0001t0006g0064 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.588+1348C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278293 | |||||||
chr21:42278402 | A | G | 238 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(235): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.588+1457A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278402 | |||||||
chr21:42278419 | A | T | 242 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.588+1474A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278419 | |||||||
chr21:42278518 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0306 |
2 | HG01496.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.588+1573G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278518 | |||||||
chr21:42278603 | C | T | 1 | a0001c0002t0002g0322 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588+1658C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278603 | |||||||
chr21:42278700 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.588+1755G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278700 | |||||||
chr21:42278704 | C | T | 9 | a0001c0003t0001g0250 a0001c0003t0003g0211 a0001c0003t0005g0044 others(6): Show |
9 | HG00408.hp1 HG01975.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+1759C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278704 | |||||||
chr21:42278705 | A | G | 209 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(206): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.588+1760A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278705 | |||||||
chr21:42278713 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.588+1768A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278713 | |||||||
chr21:42278787 | G | A | 3 | a0001c0001t0002g0277 a0001c0001t0004g0337 a0001c0001t0009g0087 |
3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+1842G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278787 | |||||||
chr21:42278792 | A | G | 89 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(86): Show |
91 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.588+1847A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278792 | |||||||
chr21:42278804 | G | C | 31 | a0001c0001t0001g0093 a0001c0001t0001g0271 a0001c0001t0001g0325 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.588+1859G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278804 | |||||||
chr21:42278830 | G | T | 1 | a0001c0002t0016g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.588+1885G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278830 | |||||||
chr21:42278840 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0004g0266 |
2 | HG01261.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.588+1895T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278840 | |||||||
chr21:42278851 | C | A | 16 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0001g0208 others(13): Show |
16 | HG00423.hp2 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.588+1906C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278851 | |||||||
chr21:42278851 | C | T | 3 | a0001c0001t0002g0277 a0001c0001t0004g0337 a0001c0001t0009g0087 |
3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+1906C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278851 | |||||||
chr21:42278857 | T | A | 60 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(57): Show |
62 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.588+1912T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278857 | |||||||
chr21:42278886 | C | T | 11 | a0001c0001t0001g0156 a0001c0001t0001g0171 a0001c0001t0001g0253 others(8): Show |
11 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+1941C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278886 | |||||||
chr21:42278958 | C | T | 93 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0099 others(90): Show |
96 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.588+2013C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278958 | |||||||
chr21:42278986 | G | A | 79 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0114 others(76): Show |
82 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.588+2041G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42278986 | |||||||
chr21:42279038 | C | T | 4 | a0001c0001t0001g0315 a0001c0001t0001g0335 a0001c0001t0029g0262 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2093C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279038 | |||||||
chr21:42279057 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.588+2112T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279057 | |||||||
chr21:42279120 | G | A | 32 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0156 others(29): Show |
33 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.588+2175G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279120 | |||||||
chr21:42279144 | A | G | 6 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+2199A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279144 | |||||||
chr21:42279180 | C | T | 63 | a0001c0001t0001g0098 a0001c0001t0001g0142 a0001c0001t0001g0155 others(60): Show |
65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.588+2235C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279180 | |||||||
chr21:42279225 | G | A | 98 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0114 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.588+2280G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279225 | |||||||
chr21:42279251 | C | T | 2 | a0001c0001t0002g0183 a0001c0001t0006g0066 |
2 | HG02683.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.588+2306C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279251 | |||||||
chr21:42279278 | G | GGAATTCT others(8): Show |
1 | a0001c0003t0005g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.588+2336_588+2350d others(17): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr21 | 42279278 | ||||||
chr21:42279298 | C | T | 3 | a0001c0001t0002g0277 a0001c0001t0004g0337 a0001c0001t0009g0087 |
3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.588+2353C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279298 | |||||||
chr21:42279313 | G | C | 2 | a0001c0001t0004g0088 a0001c0001t0004g0094 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.588+2368G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279313 | |||||||
chr21:42279318 | G | C | 2 | a0001c0001t0018g0067 a0001c0006t0001g0008 |
3 | HG01070.hp2 HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.588+2373G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279318 | |||||||
chr21:42279325 | C | T | 61 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(58): Show |
63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.588+2380C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279325 | |||||||
chr21:42279344 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.588+2399G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279344 | |||||||
chr21:42279386 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+2441G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279386 | |||||||
chr21:42279398 | T | G | 2 | a0001c0002t0002g0080 a0001c0002t0004g0274 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.588+2453T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279398 | |||||||
chr21:42279435 | A | T | 69 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0133 others(66): Show |
71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.588+2490A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279435 | |||||||
chr21:42279497 | G | A | 64 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(61): Show |
66 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.588+2552G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279497 | |||||||
chr21:42279499 | T | A | 29 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0156 others(26): Show |
29 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+2554T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279499 | |||||||
chr21:42279506 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+2561C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279506 | |||||||
chr21:42279563 | G | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0314 a0001c0001t0004g0265 |
3 | HG02280.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.588+2618G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279563 | |||||||
chr21:42279591 | C | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0193 a0001c0001t0003g0196 others(1): Show |
4 | HG01074.hp2 HG01106.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2646C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279591 | |||||||
chr21:42279598 | G | A | 1 | a0001c0001t0023g0025 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.588+2653G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279598 | |||||||
chr21:42279653 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589-2621T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279653 | |||||||
chr21:42279693 | G | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0314 a0001c0001t0004g0265 |
3 | HG02280.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.589-2581G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279693 | |||||||
chr21:42279711 | C | T | 8 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-2563C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279711 | |||||||
chr21:42279767 | T | C | 63 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(60): Show |
65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.589-2507T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279767 | |||||||
chr21:42279794 | C | T | 4 | a0001c0001t0004g0279 a0001c0001t0009g0275 a0001c0002t0002g0143 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-2480C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279794 | |||||||
chr21:42279795 | G | A | 61 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(58): Show |
63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.589-2479G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279795 | |||||||
chr21:42279864 | C | T | 61 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(58): Show |
63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.589-2410C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279864 | |||||||
chr21:42279904 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.589-2370C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279904 | |||||||
chr21:42279905 | G | T | 31 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0156 others(28): Show |
32 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.589-2369G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279905 | |||||||
chr21:42279932 | G | A | 2 | a0001c0001t0008g0194 a0001c0001t0008g0195 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.589-2342G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42279932 | |||||||
chr21:42280132 | A | C | 31 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0156 others(28): Show |
32 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.589-2142A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280132 | |||||||
chr21:42280209 | G | T | 72 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(69): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-2065G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280209 | |||||||
chr21:42280221 | T | C | 75 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0133 others(72): Show |
77 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.589-2053T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280221 | |||||||
chr21:42280250 | C | G | 72 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(69): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-2024C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280250 | |||||||
chr21:42280301 | G | C | 1 | a0001c0001t0002g0245 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.589-1973G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280301 | |||||||
chr21:42280322 | A | G | 72 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(69): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-1952A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280322 | |||||||
chr21:42280451 | T | C | 90 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(87): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1823T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280451 | |||||||
chr21:42280483 | G | A | 79 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0114 others(76): Show |
82 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.589-1791G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280483 | |||||||
chr21:42280487 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.589-1787G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280487 | |||||||
chr21:42280499 | A | G | 72 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(69): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.589-1775A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280499 | |||||||
chr21:42280527 | G | A | 2 | a0001c0001t0004g0182 a0001c0001t0004g0311 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.589-1747G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280527 | |||||||
chr21:42280596 | C | T | 26 | a0001c0001t0001g0091 a0001c0001t0001g0156 a0001c0001t0001g0171 others(23): Show |
27 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.589-1678C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280596 | |||||||
chr21:42280632 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.589-1642A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280632 | |||||||
chr21:42280666 | C | T | 62 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(59): Show |
64 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.589-1608C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280666 | |||||||
chr21:42280667 | G | A | 6 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1607G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280667 | |||||||
chr21:42280687 | C | T | 18 | a0001c0001t0001g0326 a0001c0001t0002g0092 a0001c0001t0004g0095 others(15): Show |
18 | HG01081.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-1587C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280687 | |||||||
chr21:42280713 | G | A | 3 | a0001c0001t0002g0277 a0001c0001t0004g0337 a0001c0001t0009g0087 |
3 | HG02145.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-1561G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280713 | |||||||
chr21:42280797 | C | T | 156 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(153): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.589-1477C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280797 | |||||||
chr21:42280815 | G | A | 4 | a0001c0001t0015g0285 a0001c0002t0002g0328 a0001c0002t0002g0329 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-1459G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280815 | |||||||
chr21:42280866 | A | G | 90 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(87): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1408A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280866 | |||||||
chr21:42280924 | C | T | 90 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(87): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.589-1350C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42280924 | |||||||
chr21:42281026 | G | C | 6 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1248G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281026 | |||||||
chr21:42281066 | C | T | 69 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(66): Show |
71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.589-1208C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281066 | |||||||
chr21:42281182 | C | T | 6 | a0001c0001t0011g0042 a0001c0001t0011g0045 a0001c0001t0011g0047 others(3): Show |
6 | HG01257.hp2 HG01934.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-1092C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281182 | |||||||
chr21:42281236 | G | A | 87 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(84): Show |
89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.589-1038G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281236 | |||||||
chr21:42281379 | G | T | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0308 |
3 | HG02258.hp2 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.589-895G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281379 | |||||||
chr21:42281453 | G | C | 6 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-821G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281453 | |||||||
chr21:42281521 | G | C | 1 | a0001c0001t0003g0121 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.589-753G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281521 | |||||||
chr21:42281687 | G | A | 6 | a0001c0001t0001g0336 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-587G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281687 | |||||||
chr21:42281818 | C | T | 1 | a0001c0001t0031g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-456C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281818 | |||||||
chr21:42281867 | A | G | 159 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.589-407A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281867 | |||||||
chr21:42281913 | C | T | 67 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(64): Show |
69 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.589-361C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281913 | |||||||
chr21:42281975 | A | C | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589-299A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42281975 | |||||||
chr21:42282141 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.589-133C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 5/14 | chr21 | 42282141 | |||||||
chr21:42282453 | G | A | 7 | a0001c0001t0001g0078 a0001c0001t0001g0314 a0001c0001t0004g0265 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+34G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282453 | |||||||
chr21:42282660 | G | A | 1 | a0001c0001t0004g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.734+241G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282660 | |||||||
chr21:42282738 | T | C | 246 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.734+319T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282738 | |||||||
chr21:42282744 | G | T | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.734+325G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282744 | |||||||
chr21:42282812 | A | G | 159 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.734+393A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282812 | |||||||
chr21:42282826 | G | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734+407G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282826 | |||||||
chr21:42282988 | G | A | 88 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0142 others(85): Show |
89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.734+569G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42282988 | |||||||
chr21:42283026 | G | T | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.734+607G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283026 | |||||||
chr21:42283029 | G | A | 4 | a0001c0001t0015g0285 a0001c0002t0002g0328 a0001c0002t0002g0329 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.734+610G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283029 | |||||||
chr21:42283083 | G | A | 1 | a0001c0002t0002g0330 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.734+664G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283083 | |||||||
chr21:42283115 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.734+696A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283115 | |||||||
chr21:42283214 | G | T | 28 | a0001c0001t0001g0093 a0001c0001t0001g0271 a0001c0001t0001g0325 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.734+795G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283214 | |||||||
chr21:42283246 | CTTGGGCC others(13): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.734+828_734+847del others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283246 | |||||||
chr21:42283369 | G | A | 1 | a0001c0002t0004g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.734+950G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283369 | |||||||
chr21:42283486 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.734+1067T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283486 | |||||||
chr21:42283493 | C | T | 1 | a0001c0001t0009g0221 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.735-1067C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283493 | |||||||
chr21:42283629 | GCCTGCCT others(117): Show |
G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-908_735-785del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283629 | ||||||
chr21:42283633 | GCCTGGAC others(54): Show |
G | 4 | a0001c0001t0001g0165 a0001c0001t0002g0164 a0001c0001t0023g0025 others(1): Show |
4 | HG01346.hp2 HG01975.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-908_735-848del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283633 | ||||||
chr21:42283652 | C | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-908C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283652 | |||||||
chr21:42283657 | C | A | 1 | a0001c0003t0005g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.735-903C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283657 | |||||||
chr21:42283658 | CCACCCAA others(55): Show |
C | 1 | a0001c0002t0002g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.735-900_735-839del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283658 | ||||||
chr21:42283659 | C | A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-901C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283659 | |||||||
chr21:42283660 | A | AC | 7 | a0001c0001t0001g0340 a0001c0001t0003g0073 a0001c0001t0003g0193 others(4): Show |
7 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-897dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283660 | ||||||
chr21:42283660 | A | C | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-900A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283660 | |||||||
chr21:42283660 | ACCCAAAT others(359): Show |
A | 1 | a0001c0001t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735-895_735-530del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283660 | ||||||
chr21:42283661 | CCCAAATG others(55): Show |
C | 16 | a0001c0001t0002g0229 a0001c0001t0002g0242 a0001c0001t0003g0127 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.735-896_735-835del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283661 | ||||||
chr21:42283665 | A | G | 3 | a0001c0002t0004g0274 a0001c0002t0016g0341 a0001c0003t0005g0050 |
3 | HG00408.hp1 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.735-895A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283665 | |||||||
chr21:42283665 | AATGAGTG others(56): Show |
A | 12 | a0001c0001t0001g0325 a0001c0001t0001g0336 a0001c0001t0002g0082 others(9): Show |
12 | HG01081.hp2 HG01167.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-883_735-821del others(63): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | ||||||
chr21:42283665 | AATGAGTG others(419): Show |
A | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735-883_735-458del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | ||||||
chr21:42283665 | AATGAGTG others(480): Show |
A | 1 | a0001c0001t0001g0203 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.735-883_735-397del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | ||||||
chr21:42283665 | AATGAGTG others(540): Show |
A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0142 a0001c0001t0001g0314 others(1): Show |
4 | HG02280.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-883_735-337del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283665 | ||||||
chr21:42283676 | AACCCCCA others(360): Show |
A | 2 | a0001c0001t0008g0194 a0001c0001t0008g0195 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.735-883_735-517del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283676 | |||||||
chr21:42283676 | AACCCCCA others(481): Show |
A | 2 | a0001c0001t0002g0277 a0001c0001t0009g0087 |
2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.735-883_735-396del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283676 | |||||||
chr21:42283677 | A | C | 5 | a0001c0001t0003g0073 a0001c0001t0003g0193 a0001c0001t0003g0196 others(2): Show |
5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-883A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283677 | |||||||
chr21:42283677 | ACCCCCAC others(299): Show |
A | 1 | a0001c0003t0005g0044 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.735-871_735-566del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283677 | ||||||
chr21:42283689 | T | G | 5 | a0001c0001t0003g0073 a0001c0001t0003g0193 a0001c0001t0003g0196 others(2): Show |
5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-871T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283689 | |||||||
chr21:42283693 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0193 a0001c0001t0003g0196 others(2): Show |
5 | HG00408.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-867C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283693 | |||||||
chr21:42283694 | A | G | 10 | a0001c0001t0001g0098 a0001c0001t0003g0073 a0001c0001t0003g0193 others(7): Show |
11 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-866A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283694 | |||||||
chr21:42283694 | ACCTGGAC others(56): Show |
A | 5 | a0001c0001t0002g0097 a0001c0001t0003g0323 a0001c0002t0002g0328 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-844_735-782del others(63): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | ||||||
chr21:42283694 | ACCTGGAC others(360): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.735-853_735-487del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | ||||||
chr21:42283694 | ACCTGGAC others(420): Show |
A | 1 | a0001c0001t0001g0340 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.735-853_735-427del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283694 | ||||||
chr21:42283707 | T | C | 3 | a0001c0001t0003g0228 a0001c0002t0004g0274 a0001c0002t0016g0341 |
3 | HG02615.hp2 HG03831.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.735-853T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283707 | |||||||
chr21:42283708 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-852G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283708 | |||||||
chr21:42283712 | TA | T | 30 | a0001c0001t0001g0084 a0001c0001t0001g0180 a0001c0001t0001g0192 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.735-847delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | |||||||
chr21:42283712 | TAC | T | 14 | a0001c0001t0002g0092 a0001c0001t0004g0100 a0001c0001t0004g0158 others(11): Show |
14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.735-847_735-846del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | |||||||
chr21:42283712 | TACCACCC others(58): Show |
T | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.735-847_735-783del others(65): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283712 | |||||||
chr21:42283713 | A | AC | 4 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0248 others(1): Show |
4 | HG00597.hp1 HG02056.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-845dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | ||||||
chr21:42283713 | ACCACCCA others(298): Show |
A | 1 | a0001c0001t0015g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.735-844_735-540del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | ||||||
chr21:42283713 | ACCACCCA others(419): Show |
A | 14 | a0001c0001t0001g0155 a0001c0001t0001g0278 a0001c0001t0004g0088 others(11): Show |
16 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.735-844_735-419del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283713 | ||||||
chr21:42283714 | CCA | C | 68 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0145 others(65): Show |
70 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.735-844_735-843del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283714 | ||||||
chr21:42283714 | CCACCCAC others(358): Show |
C | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.735-844_735-480del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283714 | ||||||
chr21:42283716 | A | C | 208 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(205): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.735-844A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283716 | |||||||
chr21:42283717 | C | CA | 4 | a0001c0001t0002g0147 a0001c0001t0003g0223 a0001c0001t0009g0320 others(1): Show |
4 | HG00544.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-843_735-842ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283717 | |||||||
chr21:42283720 | ACC | A | 4 | a0001c0001t0002g0190 a0001c0001t0018g0067 a0001c0003t0005g0050 others(1): Show |
4 | HG00408.hp1 HG02602.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-839_735-838del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283720 | |||||||
chr21:42283722 | CACCCAGA others(54): Show |
C | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0318 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-814_735-754del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283722 | ||||||
chr21:42283723 | ACCCAGAT others(114): Show |
A | 7 | a0001c0001t0001g0098 a0001c0001t0003g0234 a0001c0001t0003g0298 others(4): Show |
7 | HG00738.hp1 HG01934.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-814_735-694del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(171): Show |
A | 3 | a0001c0001t0002g0117 a0001c0001t0002g0183 a0001c0001t0003g0125 |
3 | HG02683.hp2 HG03704.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.735-834_735-657del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(174): Show |
A | 3 | a0001c0001t0001g0192 a0001c0002t0002g0096 a0001c0002t0002g0322 |
3 | NA18522.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.735-814_735-634del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(232): Show |
A | 3 | a0001c0001t0002g0188 a0001c0001t0002g0222 a0001c0001t0002g0293 |
3 | HG01433.hp1 HG01515.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.735-834_735-596del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(293): Show |
A | 39 | a0001c0001t0001g0110 a0001c0001t0001g0145 a0001c0001t0001g0159 others(36): Show |
40 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.735-834_735-535del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(296): Show |
A | 62 | a0001c0001t0001g0085 a0001c0001t0001g0114 a0001c0001t0001g0115 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.735-814_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(353): Show |
A | 22 | a0001c0001t0001g0093 a0001c0001t0001g0156 a0001c0001t0001g0171 others(19): Show |
22 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.735-834_735-475del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(356): Show |
A | 18 | a0001c0001t0001g0091 a0001c0001t0001g0315 a0001c0001t0003g0073 others(15): Show |
18 | HG01074.hp2 HG01106.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.735-814_735-452del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(417): Show |
A | 4 | a0001c0001t0004g0182 a0001c0001t0004g0334 a0001c0001t0030g0310 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-814_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283723 | ACCCAGAT others(477): Show |
A | 1 | a0001c0002t0004g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.735-814_735-331del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283723 | ||||||
chr21:42283725 | CCAGATGA others(51): Show |
C | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-834_735-777del others(58): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283725 | |||||||
chr21:42283728 | G | A | 17 | a0001c0001t0002g0229 a0001c0001t0002g0242 a0001c0001t0003g0127 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.735-832G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283728 | |||||||
chr21:42283739 | A | AC | 7 | a0001c0001t0002g0132 a0001c0001t0002g0220 a0001c0001t0003g0223 others(4): Show |
7 | HG00408.hp1 HG01168.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-815dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | ||||||
chr21:42283739 | ACCCCCCA others(55): Show |
A | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-804_735-743del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | ||||||
chr21:42283739 | ACCCCCCA others(115): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.735-804_735-683del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | ||||||
chr21:42283739 | ACCCCCCA others(236): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.735-804_735-562del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | ||||||
chr21:42283739 | ACCCCCCA others(297): Show |
A | 1 | a0001c0001t0013g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.735-804_735-501del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283739 | ||||||
chr21:42283740 | CCCCCCAC others(53): Show |
C | 2 | a0001c0001t0001g0231 a0001c0001t0002g0291 |
2 | HG01192.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.735-814_735-755del others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | ||||||
chr21:42283740 | CCCCCCAC others(295): Show |
C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0197 a0001c0001t0001g0205 others(4): Show |
7 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-814_735-513del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | ||||||
chr21:42283740 | CCCCCCAC others(355): Show |
C | 4 | a0001c0001t0001g0333 a0001c0001t0002g0267 a0001c0001t0011g0047 others(1): Show |
4 | HG01978.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-814_735-453del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283740 | ||||||
chr21:42283756 | T | C | 31 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0191 others(28): Show |
32 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.735-804T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283756 | |||||||
chr21:42283756 | TGCCTGGA others(55): Show |
T | 2 | a0001c0001t0009g0320 a0001c0001t0009g0321 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.735-790_735-729del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283756 | ||||||
chr21:42283770 | T | C | 4 | a0001c0001t0002g0220 a0001c0001t0006g0013 a0001c0001t0029g0262 others(1): Show |
4 | HG00408.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-790T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283770 | |||||||
chr21:42283771 | G | A | 3 | a0001c0001t0002g0220 a0001c0001t0006g0013 a0001c0003t0005g0050 |
3 | HG00408.hp1 HG02976.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.735-789G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283771 | |||||||
chr21:42283775 | TACCCCCC others(296): Show |
T | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.735-784_735-482del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283775 | |||||||
chr21:42283776 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.735-784A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283776 | |||||||
chr21:42283782 | C | A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735-778C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283782 | |||||||
chr21:42283783 | A | C | 4 | a0001c0001t0002g0220 a0001c0001t0003g0228 a0001c0001t0006g0013 others(1): Show |
4 | HG00408.hp1 HG02976.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-777A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283783 | |||||||
chr21:42283783 | AACCCAGA others(357): Show |
A | 1 | a0001c0001t0018g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735-776_735-413del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283783 | |||||||
chr21:42283784 | A | C | 1 | a0001c0001t0007g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.735-776A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283784 | |||||||
chr21:42283784 | A | G | 4 | a0001c0001t0002g0220 a0001c0001t0003g0228 a0001c0001t0006g0013 others(1): Show |
4 | HG00408.hp1 HG02976.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-776A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283784 | |||||||
chr21:42283784 | ACCCAGAT others(174): Show |
A | 2 | a0001c0001t0013g0296 a0001c0001t0023g0025 |
2 | HG01346.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.735-727_735-547del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | ||||||
chr21:42283784 | ACCCAGAT others(235): Show |
A | 9 | a0001c0001t0002g0132 a0001c0001t0002g0164 a0001c0001t0002g0302 others(6): Show |
9 | HG01069.hp1 HG01975.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.735-667_735-426del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | ||||||
chr21:42283784 | ACCCAGAT others(295): Show |
A | 1 | a0001c0003t0008g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.735-727_735-426del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | ||||||
chr21:42283784 | ACCCAGAT others(356): Show |
A | 30 | a0001c0001t0001g0210 a0001c0001t0001g0213 a0001c0001t0001g0326 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-674_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283784 | ||||||
chr21:42283789 | G | A | 11 | a0001c0001t0004g0100 a0001c0001t0004g0272 a0001c0001t0004g0281 others(8): Show |
11 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-771G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283789 | |||||||
chr21:42283800 | AC | A | 11 | a0001c0001t0003g0207 a0001c0001t0004g0272 a0001c0001t0004g0281 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-753delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | ||||||
chr21:42283800 | ACCCCCCC others(114): Show |
A | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-753_735-633del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | ||||||
chr21:42283800 | ACCCCCCC others(294): Show |
A | 1 | a0001c0001t0007g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.735-759_735-459del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283800 | |||||||
chr21:42283800 | ACCCCCCC others(357): Show |
A | 1 | a0001c0001t0004g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.735-753_735-390del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283800 | ||||||
chr21:42283801 | CCCCCCCA others(234): Show |
C | 4 | a0001c0001t0001g0248 a0001c0001t0002g0113 a0001c0001t0002g0181 others(1): Show |
4 | HG01978.hp2 HG02056.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-752_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283801 | ||||||
chr21:42283801 | CCCCCCCA others(355): Show |
C | 2 | a0001c0001t0001g0243 a0001c0001t0002g0242 |
2 | HG00642.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.735-752_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283801 | ||||||
chr21:42283802 | C | A | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-758C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283802 | |||||||
chr21:42283802 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735-758C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283802 | |||||||
chr21:42283814 | G | T | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-746G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283814 | |||||||
chr21:42283818 | C | T | 3 | a0001c0001t0003g0207 a0001c0001t0004g0337 a0001c0001t0007g0021 |
3 | HG01255.hp2 HG02148.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-742C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283818 | |||||||
chr21:42283819 | G | A | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-741G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283819 | |||||||
chr21:42283826 | C | T | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.735-734C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283826 | |||||||
chr21:42283832 | C | T | 14 | a0001c0001t0002g0092 a0001c0001t0003g0002 a0001c0001t0004g0272 others(11): Show |
15 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.735-728C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283832 | |||||||
chr21:42283833 | A | G | 18 | a0001c0001t0002g0092 a0001c0001t0002g0220 a0001c0001t0003g0002 others(15): Show |
19 | HG00408.hp1 HG01081.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.735-727A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283833 | |||||||
chr21:42283833 | AAAGTCCC others(113): Show |
A | 1 | a0001c0005t0008g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.735-716_735-597del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283833 | ||||||
chr21:42283833 | AAAGTCCC others(295): Show |
A | 1 | a0001c0001t0003g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.735-716_735-415del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283833 | ||||||
chr21:42283837 | T | TAC | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-723_735-722ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283837 | |||||||
chr21:42283837 | TCCCCCCG others(114): Show |
T | 19 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0238 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.735-667_735-547del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | ||||||
chr21:42283837 | TCCCCCCG others(175): Show |
T | 1 | a0001c0001t0002g0226 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.735-546_735-365del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | ||||||
chr21:42283837 | TCCCCCCG others(294): Show |
T | 4 | a0001c0001t0002g0092 a0001c0001t0003g0002 a0001c0001t0004g0327 others(1): Show |
5 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-722_735-422del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283837 | |||||||
chr21:42283837 | TCCCCCCG others(296): Show |
T | 3 | a0001c0001t0003g0081 a0001c0001t0003g0207 a0001c0001t0027g0342 |
3 | HG01081.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.735-614_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283837 | ||||||
chr21:42283843 | C | A | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-717C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283843 | |||||||
chr21:42283844 | G | A | 8 | a0001c0001t0004g0272 a0001c0001t0004g0281 a0001c0001t0004g0317 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-716G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283844 | |||||||
chr21:42283860 | AC | A | 7 | a0001c0001t0001g0098 a0001c0001t0004g0317 a0001c0001t0012g0313 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-693delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283860 | ||||||
chr21:42283860 | ACCCCCCC others(297): Show |
A | 2 | a0001c0001t0004g0272 a0001c0001t0004g0281 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.735-693_735-390del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283860 | ||||||
chr21:42283861 | CCCCCCCA others(113): Show |
C | 1 | a0001c0001t0003g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.735-692_735-573del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283861 | ||||||
chr21:42283861 | CCCCCCCA others(174): Show |
C | 1 | a0001c0001t0002g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.735-692_735-512del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283861 | ||||||
chr21:42283862 | C | A | 6 | a0001c0001t0004g0317 a0001c0001t0012g0313 a0001c0001t0014g0063 others(3): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-698C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283862 | |||||||
chr21:42283877 | C | T | 1 | a0001c0003t0006g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.735-683C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283877 | |||||||
chr21:42283886 | C | T | 8 | a0001c0001t0001g0325 a0001c0001t0001g0336 a0001c0001t0002g0097 others(5): Show |
8 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.735-674C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283886 | |||||||
chr21:42283892 | C | T | 22 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0191 others(19): Show |
22 | HG01167.hp1 HG02040.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.735-668C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283892 | |||||||
chr21:42283893 | A | G | 36 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0166 others(33): Show |
37 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.735-667A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283893 | |||||||
chr21:42283897 | T | TACCCCCC others(121): Show |
1 | a0001c0001t0002g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.735-663_735-662ins others(128): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | |||||||
chr21:42283897 | T | TC | 10 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0227 others(7): Show |
11 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-657dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283897 | ||||||
chr21:42283897 | TCCCCCCG others(113): Show |
T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0202 others(2): Show |
5 | NA18956.hp2 NA18973.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-662_735-543del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | |||||||
chr21:42283897 | TCCCCCCG others(234): Show |
T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0247 a0001c0001t0002g0218 |
3 | HG02071.hp2 NA18948.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.735-662_735-422del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283897 | |||||||
chr21:42283898 | C | A | 3 | a0001c0001t0001g0204 a0001c0001t0026g0316 a0001c0003t0006g0041 |
3 | HG02132.hp1 HG03098.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.735-662C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283898 | |||||||
chr21:42283898 | CCCCCCGC others(113): Show |
C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.735-656_735-537del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | ||||||
chr21:42283898 | CCCCCCGC others(174): Show |
C | 1 | a0001c0001t0014g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.735-656_735-476del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | ||||||
chr21:42283898 | CCCCCCGC others(295): Show |
C | 1 | a0001c0001t0002g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.735-656_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283898 | ||||||
chr21:42283899 | C | CCT | 7 | a0001c0001t0001g0325 a0001c0001t0001g0336 a0001c0001t0002g0097 others(4): Show |
7 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-660_735-659ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | ||||||
chr21:42283899 | CCCCCGCC others(112): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.735-656_735-538del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | ||||||
chr21:42283899 | CCCCCGCC others(173): Show |
C | 1 | a0001c0003t0006g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.735-656_735-477del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283899 | ||||||
chr21:42283900 | CCCCGCCC others(111): Show |
C | 1 | a0001c0001t0026g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.735-656_735-539del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283900 | ||||||
chr21:42283903 | C | A | 2 | a0001c0001t0002g0220 a0001c0003t0001g0250 |
2 | HG02040.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.735-657C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283903 | |||||||
chr21:42283903 | C | T | 7 | a0001c0001t0001g0325 a0001c0001t0001g0336 a0001c0001t0002g0097 others(4): Show |
7 | HG01167.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-657C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283903 | |||||||
chr21:42283904 | G | A | 6 | a0001c0001t0002g0117 a0001c0001t0002g0183 a0001c0001t0002g0220 others(3): Show |
6 | HG02040.hp1 HG02572.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-656G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283904 | |||||||
chr21:42283908 | A | G | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.735-652A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283908 | |||||||
chr21:42283909 | G | A | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-651G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283909 | |||||||
chr21:42283921 | CCCCCCCA others(295): Show |
C | 11 | a0001c0001t0002g0097 a0001c0001t0003g0323 a0001c0001t0004g0317 others(8): Show |
11 | HG02280.hp1 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-632_735-331del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283921 | ||||||
chr21:42283922 | C | A | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-638C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283922 | |||||||
chr21:42283934 | G | T | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-626G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283934 | |||||||
chr21:42283938 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-622C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283938 | |||||||
chr21:42283939 | G | A | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-621G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283939 | |||||||
chr21:42283946 | C | T | 7 | a0001c0001t0001g0098 a0001c0001t0004g0104 a0001c0001t0004g0105 others(4): Show |
8 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-614C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283946 | |||||||
chr21:42283952 | C | T | 17 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0336 others(14): Show |
18 | HG00738.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.735-608C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283952 | |||||||
chr21:42283953 | G | A | 17 | a0001c0001t0001g0084 a0001c0001t0001g0192 a0001c0001t0001g0212 others(14): Show |
18 | HG00408.hp1 HG00642.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.735-607G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283953 | |||||||
chr21:42283957 | T | TACC | 4 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0004g0268 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-603_735-602ins others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283957 | |||||||
chr21:42283957 | TC | T | 20 | a0001c0001t0001g0192 a0001c0001t0001g0212 a0001c0001t0001g0231 others(17): Show |
21 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.735-596delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283957 | ||||||
chr21:42283958 | C | CCCCCCCG others(113): Show |
1 | a0001c0001t0006g0013 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.735-547_735-546ins others(120): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283958 | ||||||
chr21:42283958 | CCCCCCCG others(235): Show |
C | 1 | a0001c0001t0001g0325 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735-553_735-312del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283958 | ||||||
chr21:42283959 | CCCCCCGC others(234): Show |
C | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-595_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283959 | ||||||
chr21:42283960 | C | CT | 6 | a0001c0001t0001g0098 a0001c0001t0001g0336 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-600_735-599ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283960 | |||||||
chr21:42283962 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-598C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283962 | |||||||
chr21:42283964 | C | A | 2 | a0001c0001t0003g0298 a0001c0001t0028g0304 |
2 | HG00738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.735-596C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283964 | |||||||
chr21:42283964 | C | T | 5 | a0001c0001t0001g0336 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-596C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283964 | |||||||
chr21:42283965 | G | A | 11 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0002g0188 others(8): Show |
11 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-595G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283965 | |||||||
chr21:42283969 | A | G | 3 | a0001c0001t0001g0336 a0001c0001t0004g0104 a0001c0001t0004g0105 |
3 | HG01891.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-591A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283969 | |||||||
chr21:42283970 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0318 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-590G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283970 | |||||||
chr21:42283981 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-579A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283981 | |||||||
chr21:42283982 | CCCCCCCA others(174): Show |
C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-571_735-391del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42283982 | ||||||
chr21:42283983 | C | A | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0318 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-577C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283983 | |||||||
chr21:42283995 | G | T | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0318 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-565G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42283995 | |||||||
chr21:42284000 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0003g0318 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-560G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284000 | |||||||
chr21:42284007 | C | T | 3 | a0001c0001t0001g0336 a0001c0001t0004g0337 a0001c0008t0011g0046 |
3 | HG01934.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-553C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284007 | |||||||
chr21:42284013 | C | T | 15 | a0001c0001t0001g0099 a0001c0001t0001g0192 a0001c0001t0001g0336 others(12): Show |
15 | HG00738.hp1 HG01891.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.735-547C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284013 | |||||||
chr21:42284014 | G | A | 10 | a0001c0001t0001g0084 a0001c0001t0001g0212 a0001c0001t0001g0290 others(7): Show |
10 | HG00280.hp2 HG01109.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.735-546G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284014 | |||||||
chr21:42284018 | T | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0202 others(2): Show |
5 | NA18956.hp2 NA18973.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-542T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | |||||||
chr21:42284018 | T | TA | 7 | a0001c0001t0001g0099 a0001c0001t0001g0192 a0001c0001t0002g0183 others(4): Show |
7 | HG00738.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-542_735-541ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | |||||||
chr21:42284018 | T | TACC | 4 | a0001c0001t0002g0219 a0001c0001t0003g0234 a0001c0001t0003g0308 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-542_735-541ins others(3): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284018 | |||||||
chr21:42284018 | TC | T | 10 | a0001c0001t0001g0084 a0001c0001t0001g0290 a0001c0001t0002g0188 others(7): Show |
10 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.735-535delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | ||||||
chr21:42284018 | TCCCCCCC others(115): Show |
T | 1 | a0001c0001t0028g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735-535_735-414del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | ||||||
chr21:42284018 | TCCCCCCC others(175): Show |
T | 1 | a0001c0001t0002g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.735-535_735-354del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284018 | ||||||
chr21:42284019 | C | A | 1 | a0001c0002t0002g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.735-541C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284019 | |||||||
chr21:42284022 | C | T | 1 | a0001c0008t0011g0046 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.735-538C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284022 | |||||||
chr21:42284022 | CCCCGCCC others(50): Show |
C | 1 | a0001c0002t0002g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.735-534_735-478del others(57): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284022 | ||||||
chr21:42284023 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.735-537C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284023 | |||||||
chr21:42284025 | C | A | 13 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0166 others(10): Show |
13 | HG01891.hp2 HG02040.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-535C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284025 | |||||||
chr21:42284025 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.735-535C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284025 | |||||||
chr21:42284026 | G | A | 59 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0001g0133 others(56): Show |
60 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.735-534G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284026 | |||||||
chr21:42284026 | G | GCCCAGAT others(178): Show |
1 | a0001c0001t0010g0006 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.735-486_735-485ins others(185): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284026 | ||||||
chr21:42284026 | G | GCCCAGAT others(179): Show |
1 | a0001c0001t0010g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.735-486_735-485ins others(186): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284026 | ||||||
chr21:42284031 | G | A | 5 | a0001c0001t0002g0219 a0001c0001t0003g0234 a0001c0001t0003g0308 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-529G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284031 | |||||||
chr21:42284039 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.735-521G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284039 | |||||||
chr21:42284042 | A | ACCCCCCC others(179): Show |
1 | a0001c0001t0010g0006 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.735-486_735-485ins others(186): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284042 | ||||||
chr21:42284042 | AC | A | 8 | a0001c0001t0002g0183 a0001c0001t0002g0219 a0001c0001t0002g0220 others(5): Show |
8 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-511delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284042 | ||||||
chr21:42284044 | C | A | 6 | a0001c0001t0002g0183 a0001c0001t0002g0219 a0001c0001t0003g0234 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-516C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284044 | |||||||
chr21:42284056 | G | T | 6 | a0001c0001t0002g0183 a0001c0001t0002g0219 a0001c0001t0003g0234 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-504G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284056 | |||||||
chr21:42284060 | C | T | 3 | a0001c0001t0002g0220 a0001c0001t0008g0194 a0001c0001t0008g0195 |
3 | HG00741.hp1 HG01192.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.735-500C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284060 | |||||||
chr21:42284061 | G | A | 6 | a0001c0001t0002g0183 a0001c0001t0002g0219 a0001c0001t0003g0234 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-499G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284061 | |||||||
chr21:42284068 | C | T | 2 | a0001c0001t0003g0223 a0001c0001t0004g0337 |
2 | HG03942.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-492C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284068 | |||||||
chr21:42284074 | C | T | 10 | a0001c0001t0002g0183 a0001c0001t0002g0219 a0001c0001t0002g0220 others(7): Show |
10 | HG02040.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.735-486C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284074 | |||||||
chr21:42284075 | A | G | 13 | a0001c0001t0001g0084 a0001c0001t0001g0335 a0001c0001t0002g0183 others(10): Show |
13 | HG01109.hp1 HG02040.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-485A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284075 | |||||||
chr21:42284079 | T | C | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.735-481T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | |||||||
chr21:42284079 | T | TAC | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0234 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-481_735-480ins others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | |||||||
chr21:42284079 | TCCCCCCG others(52): Show |
T | 1 | a0001c0003t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.735-480_735-422del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284079 | |||||||
chr21:42284079 | TCCCCCCG others(54): Show |
T | 5 | a0001c0001t0003g0318 a0001c0001t0009g0320 a0001c0001t0009g0321 others(2): Show |
5 | HG01123.hp1 HG01934.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-425_735-365del others(61): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284079 | ||||||
chr21:42284080 | C | A | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.735-480C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284080 | |||||||
chr21:42284080 | CCCCCCGC others(52): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-474_735-416del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284080 | ||||||
chr21:42284080 | CCCCCCGC others(113): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.735-474_735-355del | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284080 | ||||||
chr21:42284085 | C | A | 7 | a0001c0001t0002g0122 a0001c0001t0002g0219 a0001c0001t0002g0220 others(4): Show |
7 | HG02132.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-475C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284085 | |||||||
chr21:42284085 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735-475C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284085 | |||||||
chr21:42284086 | G | A | 33 | a0001c0001t0001g0093 a0001c0001t0001g0156 a0001c0001t0001g0171 others(30): Show |
33 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.735-474G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284086 | |||||||
chr21:42284091 | G | A | 2 | a0001c0001t0003g0308 a0001c0002t0002g0282 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-469G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284091 | |||||||
chr21:42284103 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735-457C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284103 | |||||||
chr21:42284104 | C | A | 2 | a0001c0001t0003g0308 a0001c0002t0002g0282 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-456C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284104 | |||||||
chr21:42284109 | C | A | 1 | a0001c0001t0005g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.735-451C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284109 | |||||||
chr21:42284116 | G | T | 2 | a0001c0001t0003g0308 a0001c0002t0002g0282 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-444G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284116 | |||||||
chr21:42284120 | C | T | 1 | a0001c0001t0003g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.735-440C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284120 | |||||||
chr21:42284121 | G | A | 2 | a0001c0001t0003g0308 a0001c0002t0002g0282 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.735-439G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284121 | |||||||
chr21:42284128 | C | T | 9 | a0001c0001t0001g0271 a0001c0001t0001g0335 a0001c0001t0001g0336 others(6): Show |
9 | HG01433.hp1 HG01515.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.735-432C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284128 | |||||||
chr21:42284134 | C | T | 30 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0192 others(27): Show |
30 | HG00280.hp2 HG00621.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-426C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284134 | |||||||
chr21:42284135 | G | A | 60 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.735-425G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284135 | |||||||
chr21:42284139 | T | A | 8 | a0001c0001t0001g0191 a0001c0001t0001g0247 a0001c0001t0002g0092 others(5): Show |
9 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.735-421T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284139 | |||||||
chr21:42284139 | T | TA | 19 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0192 others(16): Show |
19 | HG00280.hp2 HG01074.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.735-421_735-420ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284139 | |||||||
chr21:42284139 | TC | T | 62 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.735-414delC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284139 | ||||||
chr21:42284140 | C | CCCCCCCG others(53): Show |
1 | a0001c0001t0006g0013 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.735-371_735-312dup others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284140 | ||||||
chr21:42284140 | CCCCCCCG others(53): Show |
C | 4 | a0001c0001t0001g0212 a0001c0001t0002g0307 a0001c0002t0002g0096 others(1): Show |
4 | HG01934.hp1 HG02129.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-371_735-312del others(60): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284140 | ||||||
chr21:42284142 | C | CT | 5 | a0001c0001t0001g0271 a0001c0001t0001g0336 a0001c0001t0002g0273 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-418_735-417ins others(1): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284142 | |||||||
chr21:42284146 | C | A | 45 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0166 others(42): Show |
48 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.735-414C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | |||||||
chr21:42284146 | C | G | 1 | a0001c0001t0003g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735-414C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | |||||||
chr21:42284146 | C | T | 5 | a0001c0001t0001g0271 a0001c0001t0001g0336 a0001c0001t0002g0273 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-414C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284146 | |||||||
chr21:42284147 | G | A | 46 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0166 others(43): Show |
49 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.735-413G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284147 | |||||||
chr21:42284151 | A | G | 3 | a0001c0001t0002g0273 a0001c0001t0004g0337 a0001c0001t0015g0285 |
3 | HG02723.hp1 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.735-409A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284151 | |||||||
chr21:42284152 | G | A | 1 | a0001c0001t0003g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735-408G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284152 | |||||||
chr21:42284164 | CCCCCCCA others(52): Show |
C | 2 | a0001c0001t0001g0336 a0001c0001t0004g0337 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.735-389_735-331del others(59): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284164 | ||||||
chr21:42284165 | C | A | 4 | a0001c0001t0003g0308 a0001c0001t0004g0100 a0001c0001t0004g0272 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-395C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284165 | |||||||
chr21:42284165 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735-395C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284165 | |||||||
chr21:42284181 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.735-379C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284181 | |||||||
chr21:42284182 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.735-378G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284182 | |||||||
chr21:42284189 | C | T | 7 | a0001c0001t0002g0188 a0001c0001t0002g0222 a0001c0001t0002g0277 others(4): Show |
7 | HG01433.hp1 HG01515.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-371C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284189 | |||||||
chr21:42284195 | C | T | 7 | a0001c0001t0002g0188 a0001c0001t0002g0222 a0001c0001t0002g0277 others(4): Show |
7 | HG01433.hp1 HG01515.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-365C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284195 | |||||||
chr21:42284196 | A | G | 13 | a0001c0001t0001g0271 a0001c0001t0002g0188 a0001c0001t0002g0222 others(10): Show |
13 | HG01257.hp2 HG01433.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.735-364A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284196 | |||||||
chr21:42284202 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-358C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284202 | |||||||
chr21:42284206 | C | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735-354C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284206 | |||||||
chr21:42284206 | C | T | 3 | a0001c0001t0015g0285 a0001c0001t0017g0007 a0001c0002t0016g0341 |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-354C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284206 | |||||||
chr21:42284206 | CGCCCAGA others(55): Show |
C | 2 | a0001c0001t0004g0334 a0001c0001t0030g0310 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.735-329_735-268del others(62): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284206 | ||||||
chr21:42284211 | A | G | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.735-349A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284211 | |||||||
chr21:42284223 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.735-337A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284223 | |||||||
chr21:42284225 | C | A | 1 | a0001c0001t0003g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735-335C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284225 | |||||||
chr21:42284262 | CCT | C | 26 | a0001c0001t0002g0229 a0001c0001t0002g0242 a0001c0001t0003g0073 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.735-296_735-295del others(2): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284262 | ||||||
chr21:42284268 | T | C | 27 | a0001c0001t0002g0229 a0001c0001t0002g0242 a0001c0001t0003g0073 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.735-292T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284268 | |||||||
chr21:42284285 | A | AC | 29 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0159 others(26): Show |
30 | HG00735.hp1 HG01081.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.735-266dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr21 | 42284285 | ||||||
chr21:42284320 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0004g0264 a0001c0001t0006g0064 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-240C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284320 | |||||||
chr21:42284344 | A | T | 1 | a0001c0001t0006g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.735-216A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284344 | |||||||
chr21:42284520 | T | G | 3 | a0001c0001t0002g0273 a0001c0001t0004g0104 a0001c0001t0004g0105 |
3 | HG01891.hp1 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735-40T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284520 | |||||||
chr21:42284534 | G | A | 2 | a0001c0002t0002g0096 a0001c0002t0002g0322 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.735-26G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284534 | |||||||
chr21:42284536 | C | T | 1 | a0001c0001t0006g0014 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.735-24C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284536 | |||||||
chr21:42284540 | C | T | 86 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0093 others(83): Show |
89 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.735-20C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 6/14 | chr21 | 42284540 | |||||||
chr21:42284692 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.858+9G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284692 | |||||||
chr21:42284697 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.858+14G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284697 | |||||||
chr21:42284739 | AATGACAC others(47): Show |
A | 16 | a0001c0001t0001g0078 a0001c0001t0001g0314 a0001c0001t0002g0097 others(13): Show |
16 | HG01884.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+82_858+135delT others(53): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42284739 | ||||||
chr21:42284765 | T | A | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+82T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284765 | |||||||
chr21:42284781 | G | A | 3 | a0001c0001t0001g0325 a0001c0001t0002g0092 a0001c0001t0004g0327 |
3 | HG01081.hp1 HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+98G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284781 | |||||||
chr21:42284788 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+105G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284788 | |||||||
chr21:42284788 | GTCTTCAT others(47): Show |
G | 2 | a0001c0001t0004g0095 a0001c0001t0029g0262 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.858+148_858+201del others(54): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42284788 | ||||||
chr21:42284831 | G | C | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+148G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284831 | |||||||
chr21:42284835 | A | G | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+152A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284835 | |||||||
chr21:42284840 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+157G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284840 | |||||||
chr21:42284841 | C | T | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+158C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284841 | |||||||
chr21:42284842 | A | G | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+159A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284842 | |||||||
chr21:42284854 | C | T | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+171C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284854 | |||||||
chr21:42284871 | ACAGCCTT others(39): Show |
A | 1 | a0001c0001t0001g0209 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.858+189_858+234del others(46): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284871 | |||||||
chr21:42284872 | C | T | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+189C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284872 | |||||||
chr21:42284873 | A | G | 2 | a0001c0001t0002g0092 a0001c0001t0004g0327 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.858+190A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284873 | |||||||
chr21:42284935 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0002g0219 a0001c0001t0002g0220 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.858+252G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42284935 | |||||||
chr21:42285058 | T | C | 1 | a0001c0001t0012g0305 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.858+375T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285058 | |||||||
chr21:42285136 | G | C | 1 | a0001c0001t0002g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.858+453G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285136 | |||||||
chr21:42285173 | C | T | 1 | a0001c0001t0010g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.858+490C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285173 | |||||||
chr21:42285190 | C | G | 15 | a0001c0001t0001g0098 a0001c0001t0001g0315 a0001c0001t0001g0335 others(12): Show |
15 | HG01261.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.858+507C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285190 | |||||||
chr21:42285196 | G | C | 15 | a0001c0001t0001g0098 a0001c0001t0001g0315 a0001c0001t0001g0335 others(12): Show |
15 | HG01261.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.858+513G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285196 | |||||||
chr21:42285220 | A | G | 201 | a0001c0001t0001g0110 a0001c0001t0001g0133 a0001c0001t0001g0142 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.858+537A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285220 | |||||||
chr21:42285363 | C | T | 15 | a0001c0001t0002g0092 a0001c0001t0004g0095 a0001c0001t0004g0100 others(12): Show |
15 | HG01081.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.859-517C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285363 | |||||||
chr21:42285438 | G | A | 45 | a0001c0001t0002g0229 a0001c0001t0002g0242 a0001c0001t0003g0073 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.859-442G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285438 | |||||||
chr21:42285505 | C | CA | 6 | a0001c0001t0002g0123 a0001c0001t0002g0273 a0001c0001t0004g0104 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-362dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr21 | 42285505 | ||||||
chr21:42285615 | A | C | 202 | a0001c0001t0001g0110 a0001c0001t0001g0133 a0001c0001t0001g0142 others(199): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.859-265A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285615 | |||||||
chr21:42285741 | G | C | 5 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0002t0002g0096 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-139G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 7/14 | chr21 | 42285741 | |||||||
chr21:42286063 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0006g0287 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.973+69G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286063 | |||||||
chr21:42286204 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.973+210C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286204 | |||||||
chr21:42286486 | A | G | 4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0267 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+492A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286486 | |||||||
chr21:42286618 | C | T | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.973+624C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286618 | |||||||
chr21:42286637 | G | A | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.973+643G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286637 | |||||||
chr21:42286666 | G | A | 68 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0093 others(65): Show |
70 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.973+672G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286666 | |||||||
chr21:42286723 | C | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0001g0271 others(8): Show |
12 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.973+729C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286723 | |||||||
chr21:42286790 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.973+796A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286790 | |||||||
chr21:42286834 | T | C | 248 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0093 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.973+840T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286834 | |||||||
chr21:42286846 | G | A | 1 | a0001c0001t0006g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.973+852G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286846 | |||||||
chr21:42286885 | G | A | 20 | a0001c0001t0001g0110 a0001c0001t0001g0198 a0001c0001t0002g0109 others(17): Show |
21 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+891G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286885 | |||||||
chr21:42286991 | C | G | 182 | a0001c0001t0001g0078 a0001c0001t0001g0093 a0001c0001t0001g0098 others(179): Show |
187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.974-898C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42286991 | |||||||
chr21:42287082 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.974-807G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287082 | |||||||
chr21:42287216 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.974-673C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287216 | |||||||
chr21:42287318 | C | A | 2 | a0001c0001t0003g0073 a0001c0001t0010g0144 |
2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.974-571C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287318 | |||||||
chr21:42287345 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0005g0043 |
2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.974-544G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287345 | |||||||
chr21:42287355 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0002t0002g0270 |
3 | HG02486.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.974-534A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287355 | |||||||
chr21:42287356 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.974-533C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287356 | |||||||
chr21:42287436 | T | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0224 a0001c0001t0003g0239 others(24): Show |
29 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.974-453T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287436 | |||||||
chr21:42287481 | G | A | 1 | a0001c0001t0003g0323 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.974-408G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287481 | |||||||
chr21:42287663 | T | C | 1 | a0001c0001t0012g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.974-226T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287663 | |||||||
chr21:42287674 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.974-215G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287674 | |||||||
chr21:42287871 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.974-18C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 8/14 | chr21 | 42287871 | |||||||
chr21:42288088 | G | A | 2 | a0001c0001t0004g0269 a0001c0012t0004g0276 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1122+51G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/14 | chr21 | 42288088 | |||||||
chr21:42288170 | G | A | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0003g0118 |
3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1123-41G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 9/14 | chr21 | 42288170 | |||||||
chr21:42288321 | G | GC | 112 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0001g0284 others(109): Show |
115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1224+12dupC | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr21 | 42288321 | ||||||
chr21:42288380 | C | T | 16 | a0001c0001t0002g0273 a0001c0001t0004g0095 a0001c0001t0004g0100 others(13): Show |
16 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1224+68C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288380 | |||||||
chr21:42288407 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+95G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288407 | |||||||
chr21:42288640 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1224+328G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288640 | |||||||
chr21:42288656 | C | T | 114 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0002g0075 others(111): Show |
117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1224+344C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288656 | |||||||
chr21:42288729 | A | G | 7 | a0001c0001t0009g0087 a0001c0001t0009g0275 a0001c0001t0009g0320 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1224+417A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288729 | |||||||
chr21:42288766 | G | GAAGGA | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1224+467_1224+471d others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr21 | 42288766 | ||||||
chr21:42288814 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1224+502G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288814 | |||||||
chr21:42288880 | C | T | 131 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0001t0001g0198 others(128): Show |
134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1224+568C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288880 | |||||||
chr21:42288927 | A | T | 3 | a0001c0001t0013g0294 a0001c0001t0013g0295 a0001c0001t0013g0296 |
3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1224+615A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288927 | |||||||
chr21:42288999 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1224+687G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42288999 | |||||||
chr21:42289074 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1224+762C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289074 | |||||||
chr21:42289081 | A | G | 6 | a0001c0001t0009g0087 a0001c0001t0009g0275 a0001c0001t0009g0320 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1224+769A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289081 | |||||||
chr21:42289101 | T | C | 19 | a0001c0001t0001g0155 a0001c0001t0009g0087 a0001c0001t0009g0275 others(16): Show |
20 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1224+789T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289101 | |||||||
chr21:42289277 | G | A | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1225-773G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289277 | |||||||
chr21:42289524 | G | A | 1 | a0001c0011t0004g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1225-526G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289524 | |||||||
chr21:42289544 | G | A | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-506G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289544 | |||||||
chr21:42289556 | A | C | 104 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0002g0075 others(101): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1225-494A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289556 | |||||||
chr21:42289564 | A | G | 1 | a0001c0001t0004g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1225-486A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289564 | |||||||
chr21:42289572 | T | G | 226 | a0001c0001t0001g0098 a0001c0001t0001g0145 a0001c0001t0001g0155 others(223): Show |
233 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1225-478T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289572 | |||||||
chr21:42289590 | C | T | 84 | a0001c0001t0001g0145 a0001c0001t0001g0284 a0001c0001t0001g0326 others(81): Show |
87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1225-460C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289590 | |||||||
chr21:42289611 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1225-439G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289611 | |||||||
chr21:42289838 | G | T | 1 | a0001c0001t0026g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1225-212G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289838 | |||||||
chr21:42289845 | C | T | 2 | a0001c0001t0004g0279 a0001c0001t0014g0065 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1225-205C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289845 | |||||||
chr21:42289846 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1225-204G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289846 | |||||||
chr21:42289900 | T | A | 1 | a0001c0011t0004g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1225-150T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289900 | |||||||
chr21:42289938 | C | T | 1 | a0001c0001t0029g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-112C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289938 | |||||||
chr21:42289942 | C | T | 115 | a0001c0001t0001g0098 a0001c0001t0002g0075 a0001c0001t0002g0077 others(112): Show |
118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1225-108C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289942 | |||||||
chr21:42289984 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1225-66C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289984 | |||||||
chr21:42289986 | G | T | 115 | a0001c0001t0001g0098 a0001c0001t0002g0075 a0001c0001t0002g0077 others(112): Show |
118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1225-64G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42289986 | |||||||
chr21:42290001 | C | T | 3 | a0001c0001t0003g0111 a0001c0001t0005g0012 a0001c0001t0005g0027 |
3 | NA18612.hp1 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1225-49C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290001 | |||||||
chr21:42290020 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1225-30G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290020 | |||||||
chr21:42290045 | C | T | 1 | a0001c0003t0001g0250 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.1225-5C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 10/14 | chr21 | 42290045 | |||||||
chr21:42290232 | C | T | 1 | a0001c0002t0004g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1393+14C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290232 | |||||||
chr21:42290266 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1393+48C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290266 | |||||||
chr21:42290338 | A | T | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1393+120A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290338 | |||||||
chr21:42290549 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0171 |
2 | HG01070.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1393+331G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290549 | |||||||
chr21:42290644 | T | TG | 12 | a0001c0002t0002g0080 a0001c0002t0002g0096 a0001c0002t0002g0143 others(9): Show |
13 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1393+428dupG | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr21 | 42290644 | ||||||
chr21:42290664 | G | A | 82 | a0001c0001t0001g0145 a0001c0001t0001g0284 a0001c0001t0001g0326 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1394-428G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290664 | |||||||
chr21:42290752 | C | A | 1 | a0001c0001t0003g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1394-340C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290752 | |||||||
chr21:42290799 | C | G | 92 | a0001c0001t0001g0145 a0001c0001t0001g0284 a0001c0001t0001g0326 others(89): Show |
95 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1394-293C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290799 | |||||||
chr21:42290984 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0001g0246 others(1): Show |
4 | HG02080.hp1 HG02523.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-108G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42290984 | |||||||
chr21:42291002 | G | A | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1394-90G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 11/14 | chr21 | 42291002 | |||||||
chr21:42291258 | A | T | 9 | a0001c0002t0002g0080 a0001c0002t0002g0096 a0001c0002t0002g0143 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+66A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291258 | |||||||
chr21:42291473 | G | A | 1 | a0001c0001t0004g0266 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1495-25G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291473 | |||||||
chr21:42291475 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1495-23G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 12/14 | chr21 | 42291475 | |||||||
chr21:42291695 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG00642.hp1 HG00735.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1653+39T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291695 | |||||||
chr21:42291697 | G | GGCTTCCC others(56): Show |
1 | a0001c0001t0007g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1653+42_1653+104du others(64): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42291697 | ||||||
chr21:42291748 | C | A | 30 | a0001c0001t0001g0093 a0001c0001t0002g0092 a0001c0001t0002g0097 others(27): Show |
30 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1653+92C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291748 | |||||||
chr21:42291857 | C | A | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1653+201C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291857 | |||||||
chr21:42291879 | C | T | 13 | a0001c0001t0002g0092 a0001c0001t0002g0097 a0001c0001t0003g0081 others(10): Show |
13 | HG01081.hp2 HG01255.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1653+223C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291879 | |||||||
chr21:42291939 | G | A | 1 | a0001c0001t0003g0323 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1653+283G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291939 | |||||||
chr21:42291939 | G | T | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+283G>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291939 | |||||||
chr21:42291940 | T | G | 11 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0002t0002g0080 others(8): Show |
11 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+284T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42291940 | |||||||
chr21:42292034 | C | T | 8 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0001t0004g0169 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653+378C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292034 | |||||||
chr21:42292037 | C | T | 47 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0097 others(44): Show |
47 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1653+381C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292037 | |||||||
chr21:42292151 | T | C | 1 | a0001c0011t0004g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+495T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292151 | |||||||
chr21:42292235 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1653+579C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292235 | |||||||
chr21:42292375 | C | T | 1 | a0001c0011t0004g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+719C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292375 | |||||||
chr21:42292456 | A | G | 1 | a0001c0001t0003g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1653+800A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292456 | |||||||
chr21:42292507 | C | T | 4 | a0001c0001t0002g0097 a0001c0001t0003g0081 a0001c0001t0007g0021 others(1): Show |
4 | HG01081.hp2 HG01255.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+851C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292507 | |||||||
chr21:42292602 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1653+946A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292602 | |||||||
chr21:42292631 | A | C | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+975A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292631 | |||||||
chr21:42292632 | C | A | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1653+976C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292632 | |||||||
chr21:42292713 | ACACACTA others(53): Show |
A | 1 | a0001c0001t0007g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1653+1072_1653+113 others(64): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292713 | ||||||
chr21:42292769 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1653+1113C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292769 | |||||||
chr21:42292820 | C | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0154 a0001c0001t0004g0169 others(8): Show |
12 | HG01257.hp1 HG01258.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653+1164C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42292820 | |||||||
chr21:42292840 | ACACAGTA others(12): Show |
A | 3 | a0001c0001t0013g0294 a0001c0001t0013g0295 a0001c0001t0013g0296 |
3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1653+1189_1653+120 others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292840 | ||||||
chr21:42292961 | C | CTACACAC others(30): Show |
3 | a0001c0001t0013g0294 a0001c0001t0013g0295 a0001c0001t0013g0296 |
3 | HG02602.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1653+1342_1653+137 others(41): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42292961 | ||||||
chr21:42293072 | C | CACACACC others(5): Show |
220 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0001t0001g0200 others(217): Show |
227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1653+1427_1653+142 others(16): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293072 | ||||||
chr21:42293072 | C | CACACACC others(489): Show |
1 | a0001c0011t0004g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653+1427_1653+142 others(500): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293072 | ||||||
chr21:42293081 | CACACACT others(46): Show |
C | 1 | a0001c0001t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1654-1415_1654-136 others(57): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293081 | ||||||
chr21:42293083 | C | G | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1653+1427C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293083 | |||||||
chr21:42293097 | CACACGGT others(30): Show |
C | 1 | a0001c0001t0002g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1654-1440_1654-140 others(41): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293097 | ||||||
chr21:42293101 | C | T | 3 | a0001c0002t0004g0005 a0001c0002t0004g0274 a0001c0002t0016g0341 |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654-1441C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293101 | |||||||
chr21:42293102 | G | A | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1440G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293102 | |||||||
chr21:42293103 | G | C | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1439G>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293103 | |||||||
chr21:42293118 | T | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1424T>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293118 | |||||||
chr21:42293119 | A | G | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1423A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293119 | |||||||
chr21:42293120 | C | T | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1422C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293120 | |||||||
chr21:42293141 | T | C | 1 | a0001c0012t0004g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1654-1401T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293141 | |||||||
chr21:42293216 | C | CACA | 53 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0097 others(50): Show |
55 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1654-1325_1654-132 others(7): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293216 | ||||||
chr21:42293228 | TACACACC others(4): Show |
T | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1654-1302_1654-129 others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293228 | ||||||
chr21:42293246 | CACACTAC others(7): Show |
C | 38 | a0001c0001t0002g0277 a0001c0001t0004g0004 a0001c0001t0004g0088 others(35): Show |
40 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1654-1284_1654-127 others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293246 | ||||||
chr21:42293287 | GTACACAC others(9): Show |
G | 5 | a0001c0001t0002g0097 a0001c0001t0003g0081 a0001c0001t0004g0269 others(2): Show |
5 | HG01081.hp2 HG01255.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1241_1654-122 others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293287 | ||||||
chr21:42293317 | G | A | 10 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0273 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-1225G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293317 | |||||||
chr21:42293406 | C | T | 33 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0094 others(30): Show |
35 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1654-1136C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293406 | |||||||
chr21:42293407 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0129 |
2 | NA18944.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1654-1135G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293407 | |||||||
chr21:42293407 | G | GCACTACA others(9): Show |
1 | a0001c0003t0006g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1654-1124_1654-110 others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293407 | ||||||
chr21:42293421 | CCACACTA others(7): Show |
C | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0003g0118 |
3 | HG02080.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1654-1115_1654-110 others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293421 | ||||||
chr21:42293496 | C | T | 10 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0273 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-1046C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293496 | |||||||
chr21:42293500 | T | C | 222 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0001t0001g0200 others(219): Show |
229 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1654-1042T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293500 | |||||||
chr21:42293538 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0189 |
2 | HG00438.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1654-1004C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293538 | |||||||
chr21:42293600 | C | G | 7 | a0001c0001t0002g0237 a0001c0001t0002g0240 a0001c0001t0002g0291 others(4): Show |
7 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-942C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293600 | |||||||
chr21:42293603 | T | TACACACC others(11): Show |
3 | a0001c0001t0003g0081 a0001c0001t0004g0269 a0001c0001t0007g0021 |
3 | HG01081.hp2 HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1654-928_1654-927i others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293603 | ||||||
chr21:42293609 | CCACACTA | C | 61 | a0001c0001t0001g0098 a0001c0001t0001g0200 a0001c0001t0001g0326 others(58): Show |
64 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1654-920_1654-914d others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293609 | ||||||
chr21:42293669 | C | T | 159 | a0001c0001t0001g0098 a0001c0001t0001g0200 a0001c0001t0001g0326 others(156): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1654-873C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293669 | |||||||
chr21:42293719 | A | C | 10 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0273 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-823A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293719 | |||||||
chr21:42293750 | A | G | 1 | a0001c0007t0015g0346 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1654-792A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293750 | |||||||
chr21:42293756 | TACATACC | T | 12 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0273 others(9): Show |
12 | HG01081.hp2 HG01255.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1654-775_1654-769d others(9): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293756 | ||||||
chr21:42293791 | C | T | 1 | a0001c0001t0017g0007 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1654-751C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293791 | |||||||
chr21:42293831 | G | A | 53 | a0001c0001t0001g0155 a0001c0001t0002g0092 a0001c0001t0002g0097 others(50): Show |
55 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1654-711G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293831 | |||||||
chr21:42293877 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1654-665A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293877 | |||||||
chr21:42293891 | C | A | 1 | a0001c0001t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1654-651C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293891 | |||||||
chr21:42293921 | A | G | 5 | a0001c0001t0002g0083 a0001c0001t0002g0134 a0001c0001t0002g0137 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-621A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293921 | |||||||
chr21:42293923 | A | C | 5 | a0001c0001t0002g0083 a0001c0001t0002g0134 a0001c0001t0002g0137 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-619A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293923 | |||||||
chr21:42293927 | ACCACACA others(29): Show |
A | 6 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0134 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1654-607_1654-572d others(38): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293927 | ||||||
chr21:42293950 | A | ACCACACA others(6): Show |
3 | a0001c0001t0004g0004 a0001c0001t0011g0042 a0001c0001t0022g0024 |
4 | HG01257.hp1 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-557_1654-545d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293950 | ||||||
chr21:42293950 | ACCACACA others(6): Show |
A | 187 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0098 others(184): Show |
193 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1654-557_1654-545d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr21 | 42293950 | ||||||
chr21:42293998 | C | A | 1 | a0001c0001t0002g0082 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1654-544C>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42293998 | |||||||
chr21:42294064 | G | A | 2 | a0001c0002t0002g0080 a0001c0002t0002g0270 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1654-478G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294064 | |||||||
chr21:42294095 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1654-447C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294095 | |||||||
chr21:42294204 | A | G | 2 | a0001c0001t0009g0320 a0001c0001t0009g0321 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1654-338A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294204 | |||||||
chr21:42294211 | C | G | 14 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0094 others(11): Show |
15 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1654-331C>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294211 | |||||||
chr21:42294407 | A | C | 220 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0199 others(217): Show |
227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1654-135A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294407 | |||||||
chr21:42294437 | A | T | 4 | a0001c0001t0002g0277 a0001c0001t0004g0279 a0001c0001t0012g0313 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-105A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294437 | |||||||
chr21:42294456 | G | A | 2 | a0001c0002t0002g0096 a0001c0002t0002g0322 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1654-86G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294456 | |||||||
chr21:42294469 | G | A | 30 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0093 others(27): Show |
31 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1654-73G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 13/14 | chr21 | 42294469 | |||||||
chr21:42294670 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1772+10G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294670 | |||||||
chr21:42294733 | G | A | 1 | a0001c0001t0004g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1772+73G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294733 | |||||||
chr21:42294825 | C | T | 8 | a0001c0001t0003g0073 a0001c0001t0003g0186 a0001c0001t0003g0193 others(5): Show |
8 | HG01074.hp2 HG01106.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1772+165C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294825 | |||||||
chr21:42294887 | G | A | 3 | a0001c0001t0002g0097 a0001c0001t0029g0262 a0001c0002t0016g0341 |
3 | HG02615.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1772+227G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294887 | |||||||
chr21:42294903 | A | C | 214 | a0001c0001t0001g0200 a0001c0001t0002g0075 a0001c0001t0002g0077 others(211): Show |
221 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1772+243A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294903 | |||||||
chr21:42294937 | C | T | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+277C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294937 | |||||||
chr21:42294978 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1772+318C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42294978 | |||||||
chr21:42295019 | T | C | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+359T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295019 | |||||||
chr21:42295046 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0235 others(1): Show |
4 | HG02027.hp2 HG02083.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1772+386C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295046 | |||||||
chr21:42295059 | G | A | 1 | a0001c0001t0003g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1772+399G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295059 | |||||||
chr21:42295066 | A | C | 3 | a0001c0001t0010g0144 a0001c0001t0010g0167 a0001c0001t0010g0292 |
3 | HG01123.hp1 HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+406A>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295066 | |||||||
chr21:42295191 | C | T | 12 | a0001c0001t0004g0004 a0001c0001t0004g0154 a0001c0001t0004g0169 others(9): Show |
13 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+531C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295191 | |||||||
chr21:42295228 | C | T | 161 | a0001c0001t0001g0200 a0001c0001t0002g0075 a0001c0001t0002g0077 others(158): Show |
166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1772+568C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295228 | |||||||
chr21:42295286 | G | A | 9 | a0001c0001t0002g0092 a0001c0001t0002g0273 a0001c0002t0002g0080 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1772+626G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295286 | |||||||
chr21:42295325 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1772+665C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295325 | |||||||
chr21:42295333 | T | TA | 17 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0198 others(14): Show |
17 | HG00609.hp1 HG01257.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1772+717dupA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1772+708_1772+717d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0139 a0001c0001t0006g0018 a0001c0001t0006g0040 |
3 | HG02698.hp1 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1772+707_1772+717d others(13): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | T | TAAAAAAA others(5): Show |
1 | a0001c0003t0006g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1772+706_1772+717d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TA | T | 16 | a0001c0001t0001g0128 a0001c0001t0001g0159 a0001c0001t0001g0191 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1772+717delA | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAA | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0155 others(4): Show |
7 | HG01884.hp1 HG02922.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1772+716_1772+717d others(4): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0010g0144 a0001c0001t0010g0167 |
2 | HG01123.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1772+708_1772+717d others(12): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0009g0320 a0001c0001t0009g0331 |
2 | HG02055.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1772+707_1772+717d others(13): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(5): Show |
T | 5 | a0001c0001t0002g0303 a0001c0001t0003g0323 a0001c0001t0009g0087 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+706_1772+717d others(14): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1772+705_1772+717d others(15): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(7): Show |
T | 11 | a0001c0001t0001g0336 a0001c0001t0002g0230 a0001c0001t0002g0286 others(8): Show |
11 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1772+704_1772+717d others(16): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(8): Show |
T | 30 | a0001c0001t0002g0082 a0001c0001t0002g0097 a0001c0001t0002g0113 others(27): Show |
30 | HG00423.hp1 HG00544.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1772+703_1772+717d others(17): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(9): Show |
T | 120 | a0001c0001t0001g0200 a0001c0001t0002g0075 a0001c0001t0002g0077 others(117): Show |
125 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1772+702_1772+717d others(18): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(10): Show |
T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG00099.hp1 HG00597.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1772+701_1772+717d others(19): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(11): Show |
T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0205 a0001c0001t0006g0051 others(1): Show |
4 | HG01261.hp1 NA18957.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1772+700_1772+717d others(20): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(12): Show |
T | 13 | a0001c0001t0001g0099 a0001c0001t0001g0142 a0001c0001t0001g0171 others(10): Show |
13 | HG00738.hp2 HG01167.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+699_1772+717d others(21): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(13): Show |
T | 20 | a0001c0001t0001g0156 a0001c0001t0002g0092 a0001c0001t0002g0273 others(17): Show |
21 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1772+698_1772+717d others(22): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(14): Show |
T | 3 | a0001c0001t0001g0326 a0001c0002t0002g0143 a0001c0002t0002g0328 |
3 | HG02451.hp1 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1772+697_1772+717d others(23): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(15): Show |
T | 5 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0001t0004g0279 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+696_1772+717d others(24): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(16): Show |
T | 4 | a0001c0002t0004g0005 a0001c0002t0004g0274 a0001c0002t0016g0341 others(1): Show |
5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1772+695_1772+717d others(25): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(17): Show |
T | 17 | a0001c0001t0002g0277 a0001c0001t0004g0095 a0001c0001t0004g0100 others(14): Show |
17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1772+694_1772+717d others(26): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295333 | TAAAAAAA others(19): Show |
T | 1 | a0001c0001t0001g0260 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1772+692_1772+717d others(28): Show |
ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr21 | 42295333 | ||||||
chr21:42295345 | A | T | 1 | a0001c0001t0009g0320 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1772+685A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295345 | |||||||
chr21:42295346 | A | T | 1 | a0001c0001t0009g0321 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1772+686A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295346 | |||||||
chr21:42295422 | T | A | 1 | a0001c0001t0004g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1773-742T>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295422 | |||||||
chr21:42295463 | A | T | 2 | a0001c0002t0002g0096 a0001c0002t0002g0322 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1773-701A>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295463 | |||||||
chr21:42295479 | C | T | 1 | a0001c0001t0005g0012 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1773-685C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295479 | |||||||
chr21:42295485 | G | A | 13 | a0001c0001t0004g0004 a0001c0001t0004g0154 a0001c0001t0004g0169 others(10): Show |
14 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1773-679G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295485 | |||||||
chr21:42295629 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1773-535A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295629 | |||||||
chr21:42295691 | T | C | 50 | a0001c0001t0002g0092 a0001c0001t0002g0273 a0001c0001t0002g0277 others(47): Show |
52 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.1773-473T>C | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295691 | |||||||
chr21:42295749 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1773-415C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295749 | |||||||
chr21:42295912 | G | A | 162 | a0001c0001t0002g0075 a0001c0001t0002g0077 a0001c0001t0002g0082 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1773-252G>A | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295912 | |||||||
chr21:42295988 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1773-176C>T | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42295988 | |||||||
chr21:42296131 | A | G | 52 | a0001c0001t0002g0092 a0001c0001t0002g0273 a0001c0001t0002g0277 others(49): Show |
54 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.1773-33A>G | ABCG1 | ENSG00000160179.19 | transcript | ENST00000398449.8 | protein_coding | 14/14 | chr21 | 42296131 |