Item | Value |
---|---|
geneid | 5243 |
ensemblid | ENSG00000085563.15 |
hgncid | 40 |
symbol | ABCB1 |
name | ATP binding cassette subfamily B member 1 |
refseq_nuc | NM_001348946.2 |
refseq_prot | NP_001335875.1 |
ensembl_nuc | ENST00000622132.5 |
ensembl_prot | ENSP00000478255.1 |
mane_status | MANE Select |
chr | chr7 |
start | 87503017 |
end | 87600884 |
strand | - |
ver | v1.2 |
region | chr7:87503017-87600884 |
region5000 | chr7:87498017-87605884 |
regionname0 | ABCB1_chr7_87503017_87600884 |
regionname5000 | ABCB1_chr7_87498017_87605884 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1280 | 247 | 78 | 47 | 95 | 10 | 17 | 63 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0002 | 1/0 | 1280 | 74 | 4 | 12 | 38 | 4 | 15 | 29 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0003 | 0/0 | 1280 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0004 | 0/0 | 1280 | 4 | 0 | 2 | 2 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0005 | 0/0 | 1280 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0006 | 0/0 | 1280 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0007 | 0/0 | 1280 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0008 | 0/0 | 1280 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0009 | 0/0 | 1280 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0010 | 0/0 | 1280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0011 | 0/0 | 1280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0012 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0013 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0014 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0015 | 0/0 | 1280 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0016 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0017 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0018 | 0/0 | 1280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
a0019 | 0/1 | 1280 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | MDLEG others(1275): Show |
chr7 | 87498017 | 87605884 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3840 | 144 | 66 | 27 | 31 | 9 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0003 | 0/0 | 3840 | 35 | 3 | 4 | 27 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0004 | 0/0 | 3840 | 34 | 0 | 6 | 26 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0005 | 0/0 | 3840 | 23 | 1 | 9 | 10 | 1 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0006 | 0/0 | 3840 | 7 | 6 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0018 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0020 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0022 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0001c0025 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0002c0002 | 1/0 | 3840 | 66 | 3 | 10 | 37 | 4 | 11 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0002c0009 | 0/0 | 3840 | 4 | 0 | 1 | 1 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0002c0010 | 0/0 | 3840 | 3 | 0 | 1 | 0 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0002c0024 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0003c0007 | 0/0 | 3840 | 5 | 4 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0004c0008 | 0/0 | 3840 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0005c0012 | 0/0 | 3840 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0005c0017 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0006c0011 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0007c0014 | 0/0 | 3840 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0008c0013 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0009c0030 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0009c0031 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0010c0028 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0011c0029 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0012c0021 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0013c0026 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0014c0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0015c0027 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0016c0015 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0017c0032 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0018c0016 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 | ||
a0019c0023 | 0/1 | 3840 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATGGA others(3835): Show |
chr7 | 87498017 | 87605884 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5205 | 88 | 38 | 16 | 23 | 5 | 6 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0002 | 0/0 | 5205 | 11 | 2 | 2 | 6 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0003 | 0/0 | 5205 | 12 | 3 | 4 | 2 | 1 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0004 | 0/0 | 5205 | 13 | 8 | 4 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0005 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0006 | 0/0 | 5213 | 6 | 6 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0007 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0008 | 0/0 | 5201 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5196): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0010 | 0/0 | 5205 | 2 | 1 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0011 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0015 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0018 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0019 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0021 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0001t0022 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0003t0001 | 0/0 | 5205 | 23 | 0 | 4 | 18 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0003t0002 | 0/0 | 5205 | 9 | 0 | 0 | 9 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0003t0006 | 0/0 | 5213 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0003t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0004t0001 | 0/0 | 5205 | 2 | 0 | 1 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0004t0002 | 0/0 | 5205 | 20 | 0 | 5 | 13 | 0 | 2 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0004t0005 | 0/0 | 5205 | 9 | 0 | 0 | 9 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0004t0012 | 0/0 | 5205 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0004t0020 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0001 | 0/0 | 5205 | 13 | 0 | 4 | 8 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0002 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0003 | 0/0 | 5205 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0005 | 0/0 | 5205 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0007 | 0/0 | 5205 | 4 | 0 | 3 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0005t0016 | 0/0 | 5201 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5196): Show |
chr7 | 87498017 | 87605884 |
a0001c0006t0001 | 0/0 | 5205 | 2 | 1 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0006t0003 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0006t0004 | 0/0 | 5205 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0018t0017 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0001c0020t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0022t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0001c0025t0001 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0002t0001 | 0/0 | 5205 | 56 | 3 | 10 | 30 | 3 | 10 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0002t0002 | 0/0 | 5205 | 7 | 0 | 0 | 6 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0002t0007 | 1/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0002t0011 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5208): Show |
chr7 | 87498017 | 87605884 |
a0002c0002t0013 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0009t0001 | 0/0 | 5205 | 2 | 0 | 1 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0009t0002 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0009t0013 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0010t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0010t0002 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0010t0003 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0002c0024t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0003c0007t0001 | 0/0 | 5205 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0003c0007t0003 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0003c0007t0008 | 0/0 | 5201 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5196): Show |
chr7 | 87498017 | 87605884 |
a0004c0008t0001 | 0/0 | 5205 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0005c0012t0001 | 0/0 | 5205 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0005c0017t0002 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0006c0011t0001 | 0/0 | 5205 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0007c0014t0001 | 0/0 | 5205 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0008c0013t0001 | 0/0 | 5205 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0009c0030t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0009c0031t0002 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0010c0028t0001 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0011c0029t0002 | 0/0 | 5205 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0012c0021t0001 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0013c0026t0014 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0014c0019t0009 | 0/0 | 5205 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0015c0027t0001 | 0/0 | 5205 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0016c0015t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0017c0032t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0018c0016t0001 | 0/0 | 5205 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
a0019c0023t0001 | 0/1 | 5205 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | ATTCG others(5200): Show |
chr7 | 87498017 | 87605884 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0021g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0001t0022g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0003t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0004t0020g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0005t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0006t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0018t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0020t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0022t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0001c0025t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0007g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0002t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0009t0013g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0010t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0002c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0007t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0007t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0007t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0003c0007t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0008t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0008t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0008t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0004c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0012t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0012t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0005c0017t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0011t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0011t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0006c0011t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0007c0014t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0007c0014t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0008c0013t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0008c0013t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0009c0030t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0009c0031t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0010c0028t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0011c0029t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0012c0021t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0013c0026t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0014c0019t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0015c0027t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0016c0015t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0017c0032t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0018c0016t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
a0019c0023t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | GBR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00280 | hp2 | a0001 | c0005 | t0007 | g0076 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0078 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0329 | EUR | FIN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00423 | hp2 | a0001 | c0004 | t0005 | g0019 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00544 | hp2 | a0001 | c0003 | t0002 | g0245 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0318 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0141 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00609 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00609 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00639 | hp1 | a0003 | c0007 | t0001 | g0258 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00741 | hp1 | a0005 | c0012 | t0001 | g0273 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG00741 | hp2 | a0002 | c0009 | t0001 | g0128 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01069 | hp2 | a0001 | c0005 | t0003 | g0003 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01070 | hp1 | a0001 | c0005 | t0007 | g0004 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01071 | hp1 | a0001 | c0005 | t0003 | g0003 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01071 | hp2 | a0001 | c0005 | t0007 | g0004 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01081 | hp2 | a0001 | c0005 | t0007 | g0079 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01106 | hp1 | a0005 | c0012 | t0001 | g0271 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0328 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01109 | hp1 | a0005 | c0017 | t0002 | g0272 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01169 | hp2 | a0001 | c0005 | t0001 | g0276 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01192 | hp1 | a0001 | c0004 | t0001 | g0071 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01255 | hp1 | a0007 | c0014 | t0001 | g0339 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01258 | hp2 | a0010 | c0028 | t0001 | g0146 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01261 | hp1 | a0002 | c0010 | t0001 | g0090 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01261 | hp2 | a0004 | c0008 | t0001 | g0187 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01358 | hp2 | a0001 | c0004 | t0002 | g0046 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01496 | hp1 | a0011 | c0029 | t0002 | g0130 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01496 | hp2 | a0001 | c0004 | t0002 | g0044 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0335 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0336 | EUR | IBS | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01928 | hp1 | a0004 | c0008 | t0001 | g0199 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01952 | hp1 | a0001 | c0020 | t0001 | g0042 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0222 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0319 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01978 | hp1 | a0001 | c0004 | t0002 | g0041 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01981 | hp1 | a0001 | c0004 | t0002 | g0045 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01981 | hp2 | a0001 | c0005 | t0001 | g0196 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01993 | hp2 | a0001 | c0001 | t0018 | g0281 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02015 | hp2 | a0001 | c0005 | t0001 | g0212 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02027 | hp2 | a0001 | c0005 | t0001 | g0293 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02040 | hp2 | a0001 | c0005 | t0001 | g0211 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02129 | hp2 | a0001 | c0004 | t0002 | g0054 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02145 | hp1 | a0008 | c0013 | t0001 | g0262 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02155 | hp2 | a0001 | c0004 | t0002 | g0107 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02165 | hp2 | a0002 | c0002 | t0013 | g0140 | EAS | CDX | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0331 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02572 | hp1 | a0003 | c0007 | t0003 | g0033 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02572 | hp2 | a0001 | c0005 | t0016 | g0096 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02615 | hp2 | a0001 | c0022 | t0001 | g0268 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02622 | hp2 | a0001 | c0006 | t0003 | g0023 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02647 | hp1 | a0003 | c0007 | t0001 | g0102 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02647 | hp2 | a0006 | c0011 | t0001 | g0092 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0131 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02698 | hp2 | a0001 | c0025 | t0001 | g0122 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02717 | hp2 | a0001 | c0006 | t0001 | g0104 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02723 | hp1 | a0001 | c0018 | t0017 | g0039 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02886 | hp2 | a0003 | c0007 | t0008 | g0334 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02965 | hp2 | a0001 | c0006 | t0004 | g0009 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02970 | hp2 | a0012 | c0021 | t0001 | g0307 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03041 | hp1 | a0001 | c0006 | t0004 | g0327 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03098 | hp2 | a0013 | c0026 | t0014 | g0010 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03195 | hp1 | a0008 | c0013 | t0001 | g0189 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03209 | hp2 | a0001 | c0006 | t0004 | g0103 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03225 | hp2 | a0002 | c0024 | t0001 | g0184 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03239 | hp1 | a0007 | c0014 | t0001 | g0340 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03453 | hp1 | a0001 | c0003 | t0009 | g0113 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03491 | hp2 | a0001 | c0005 | t0005 | g0025 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03516 | hp1 | a0014 | c0019 | t0009 | g0237 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03540 | hp1 | a0001 | c0001 | t0021 | g0341 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03540 | hp2 | a0006 | c0011 | t0001 | g0094 | AFR | GWD | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03654 | hp1 | a0001 | c0004 | t0002 | g0072 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03669 | hp1 | a0002 | c0002 | t0011 | g0162 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0249 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03704 | hp1 | a0002 | c0010 | t0003 | g0030 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03834 | hp1 | a0001 | c0004 | t0002 | g0134 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0164 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03942 | hp2 | a0002 | c0009 | t0002 | g0177 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04184 | hp2 | a0015 | c0027 | t0001 | g0280 | SAS | BEB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04199 | hp2 | a0002 | c0010 | t0002 | g0070 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04228 | hp1 | a0001 | c0001 | t0015 | g0028 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG04228 | hp2 | a0002 | c0009 | t0013 | g0277 | SAS | STU | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18612 | hp2 | a0009 | c0031 | t0002 | g0241 | EAS | CHB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18940 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18941 | hp2 | a0002 | c0009 | t0001 | g0323 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18948 | hp1 | a0001 | c0004 | t0002 | g0174 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18948 | hp2 | a0001 | c0005 | t0001 | g0284 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18949 | hp1 | a0016 | c0015 | t0001 | g0080 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18952 | hp2 | a0001 | c0004 | t0005 | g0022 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18963 | hp2 | a0001 | c0004 | t0005 | g0015 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18964 | hp1 | a0001 | c0004 | t0002 | g0270 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18970 | hp2 | a0001 | c0004 | t0005 | g0012 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18971 | hp2 | a0001 | c0004 | t0002 | g0251 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18973 | hp1 | a0001 | c0004 | t0002 | g0064 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18977 | hp1 | a0001 | c0004 | t0002 | g0048 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18979 | hp1 | a0001 | c0005 | t0001 | g0285 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18979 | hp2 | a0001 | c0004 | t0020 | g0057 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18988 | hp1 | a0001 | c0005 | t0001 | g0304 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18988 | hp2 | a0001 | c0004 | t0005 | g0013 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0243 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18990 | hp2 | a0001 | c0004 | t0005 | g0016 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18992 | hp1 | a0001 | c0004 | t0005 | g0014 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18994 | hp2 | a0001 | c0004 | t0002 | g0052 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18998 | hp1 | a0001 | c0005 | t0005 | g0021 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0235 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19001 | hp1 | a0001 | c0004 | t0002 | g0075 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19003 | hp1 | a0001 | c0004 | t0005 | g0017 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19003 | hp2 | a0001 | c0005 | t0001 | g0126 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19004 | hp2 | a0001 | c0005 | t0001 | g0209 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19005 | hp2 | a0001 | c0004 | t0002 | g0067 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19010 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19011 | hp1 | a0009 | c0030 | t0001 | g0242 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19056 | hp2 | a0001 | c0004 | t0002 | g0047 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19060 | hp1 | a0017 | c0032 | t0001 | g0110 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19063 | hp2 | a0001 | c0004 | t0002 | g0053 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19077 | hp1 | a0001 | c0005 | t0002 | g0300 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19082 | hp2 | a0001 | c0004 | t0005 | g0011 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19083 | hp1 | a0001 | c0004 | t0002 | g0050 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19088 | hp2 | a0001 | c0004 | t0012 | g0133 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19091 | hp1 | a0004 | c0008 | t0001 | g0215 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19091 | hp2 | a0018 | c0016 | t0001 | g0040 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0342 | AFR | YRI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | ASW | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0121 | EUR | TSI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0026 | EUR | TSI | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | GIH | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | GIH | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01123 | hp1 | a0001 | c0005 | t0001 | g0314 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG01123 | hp2 | a0001 | c0004 | t0002 | g0069 | AMR | CLM | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02109 | hp1 | a0003 | c0007 | t0008 | g0333 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG02559 | hp2 | a0001 | c0003 | t0006 | g0062 | AFR | ACB | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03471 | hp1 | a0001 | c0003 | t0006 | g0081 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG06807 | hp1 | a0006 | c0011 | t0001 | g0093 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18955 | hp1 | a0004 | c0008 | t0001 | g0217 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA18955 | hp2 | a0001 | c0004 | t0012 | g0132 | EAS | JPT | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | USA | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA21309 | hp1 | a0001 | c0006 | t0004 | g0009 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
NA21309 | hp2 | a0001 | c0001 | t0019 | g0311 | AFR | LWK | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
homoSapiens | chm13v2 | a0019 | c0023 | t0001 | g0106 | REF | REF | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
homoSapiens | grch38p0 | a0002 | c0002 | t0007 | g0077 | REF | REF | ABCB1_chr7_87498017_87605884 | ABCB1 | chr7 | 87498017 | 87605884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504251 | G | A | 1 | a0012 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3835C>T | p.Arg1279Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3971/5205 | 3835/3843 | 1279/1280 | chr7 | 87504251 | |||
chr7:87504335 | C | T | 1 | a0004 | 4 | HG01261.hp2 HG01928.hp1 NA18955.hp1 others(1): Show |
missense_variant | MODERATE | c.3751G>A | p.Val1251Ile | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3887/5205 | 3751/3843 | 1251/1280 | chr7 | 87504335 | |||
chr7:87509343 | A | T | 1 | a0003 | 5 | HG00639.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
missense_variant | MODERATE | c.3421T>A | p.Ser1141Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3557/5205 | 3421/3843 | 1141/1280 | chr7 | 87509343 | |||
chr7:87509442 | A | G | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3322T>C | p.Trp1108Arg | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3458/5205 | 3322/3843 | 1108/1280 | chr7 | 87509442 | |||
chr7:87509444 | T | G | 1 | a0010 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.3320A>C | p.Gln1107Pro | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3456/5205 | 3320/3843 | 1107/1280 | chr7 | 87509444 | |||
chr7:87515251 | C | T | 1 | a0008 | 2 | HG02145.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.3262G>A | p.Asp1088Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/28 | 3398/5205 | 3262/3843 | 1088/1280 | chr7 | 87515251 | |||
chr7:87519444 | T | G | 1 | a0011 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2809A>C | p.Ile937Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/28 | 2945/5205 | 2809/3843 | 937/1280 | chr7 | 87519444 | |||
chr7:87531302 | A | C | 12 | a0001 a0003 a0004 others(9): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
missense_variant | MODERATE | c.2677T>G | p.Ser893Ala | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2813/5205 | 2677/3843 | 893/1280 | chr7 | 87531302 | |||
chr7:87531302 | A | T | 2 | a0001 a0018 |
36 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(33): Show |
missense_variant | MODERATE | c.2677T>A | p.Ser893Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2813/5205 | 2677/3843 | 893/1280 | chr7 | 87531302 | |||
chr7:87531358 | A | G | 1 | a0014 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2621T>C | p.Val874Ala | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/28 | 2757/5205 | 2621/3843 | 874/1280 | chr7 | 87531358 | |||
chr7:87539281 | G | C | 1 | a0009 | 2 | NA18612.hp2 NA19011.hp1 |
missense_variant | MODERATE | c.2384C>G | p.Ser795Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/28 | 2520/5205 | 2384/3843 | 795/1280 | chr7 | 87539281 | |||
chr7:87544882 | G | A | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2005C>T | p.Arg669Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/28 | 2141/5205 | 2005/3843 | 669/1280 | chr7 | 87544882 | |||
chr7:87545988 | G | A | 1 | a0015 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1762C>T | p.Arg588Cys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/28 | 1898/5205 | 1762/3843 | 588/1280 | chr7 | 87545988 | |||
chr7:87550493 | C | T | 1 | a0005 | 3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
missense_variant | MODERATE | c.1199G>A | p.Ser400Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/28 | 1335/5205 | 1199/3843 | 400/1280 | chr7 | 87550493 | |||
chr7:87561309 | T | C | 1 | a0006 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.781A>G | p.Ile261Val | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/28 | 917/5205 | 781/3843 | 261/1280 | chr7 | 87561309 | |||
chr7:87570185 | C | T | 1 | a0018 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.325G>A | p.Glu109Lys | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/28 | 461/5205 | 325/3843 | 109/1280 | chr7 | 87570185 | |||
chr7:87585654 | C | A | 1 | a0017 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.144G>T | p.Lys48Asn | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/28 | 280/5205 | 144/3843 | 48/1280 | chr7 | 87585654 | |||
chr7:87600124 | T | C | 1 | a0007 | 2 | HG01255.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.61A>G | p.Asn21Asp | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 197/5205 | 61/3843 | 21/1280 | chr7 | 87600124 | |||
chr7:87600136 | A | G | 1 | a0016 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.49T>C | p.Phe17Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 185/5205 | 49/3843 | 17/1280 | chr7 | 87600136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504258 | T | C | 1 | a0001c0022 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.3828A>G | p.Gly1276Gly | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 3964/5205 | 3828/3843 | 1276/1280 | chr7 | 87504258 | |||
chr7:87509329 | A | G | 20 | a0001c0001 a0001c0003 a0001c0004 others(17): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
synonymous_variant | LOW | c.3435T>C | p.Ile1145Ile | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/28 | 3571/5205 | 3435/3843 | 1145/1280 | chr7 | 87509329 | |||
chr7:87541369 | T | C | 1 | a0001c0025 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2307A>G | p.Thr769Thr | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/28 | 2443/5205 | 2307/3843 | 769/1280 | chr7 | 87541369 | |||
chr7:87549411 | C | G | 1 | a0001c0018 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1662G>C | p.Leu554Leu | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/28 | 1798/5205 | 1662/3843 | 554/1280 | chr7 | 87549411 | |||
chr7:87550285 | A | G | 19 | a0001c0001 a0001c0004 a0001c0005 others(16): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
synonymous_variant | LOW | c.1236T>C | p.Gly412Gly | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/28 | 1372/5205 | 1236/3843 | 412/1280 | chr7 | 87550285 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87503314 | C | G | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*929G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 929 | chr7 | 87503314 | ||||||
chr7:87503509 | C | G | 1 | a0001c0001t0018 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*734G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 734 | chr7 | 87503509 | ||||||
chr7:87503600 | C | T | 27 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(24): Show |
98 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*643G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 643 | chr7 | 87503600 | ||||||
chr7:87503888 | A | G | 1 | a0001c0004t0012 | 2 | NA18955.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*355T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 355 | chr7 | 87503888 | ||||||
chr7:87503991 | T | G | 3 | a0001c0001t0009 a0001c0003t0009 a0014c0019t0009 |
3 | HG03195.hp2 HG03453.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 252 | chr7 | 87503991 | ||||||
chr7:87504050 | T | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(17): Show |
88 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*193A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 193 | chr7 | 87504050 | ||||||
chr7:87504070 | A | ATGTCTCT others(1): Show |
7 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0015 others(4): Show |
13 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*165_*172dupGAGAGA others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 172 | chr7 | 87504070 | ||||||
chr7:87504097 | C | T | 4 | a0001c0001t0008 a0001c0005t0016 a0003c0007t0008 others(1): Show |
7 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 146 | chr7 | 87504097 | ||||||
chr7:87504154 | T | A | 3 | a0001c0001t0004 a0001c0001t0010 a0001c0006t0004 |
19 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*89A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 89 | chr7 | 87504154 | ||||||
chr7:87504160 | TGTAA | T | 3 | a0001c0001t0008 a0001c0005t0016 a0003c0007t0008 |
6 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*79_*82delTTAC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 79 | chr7 | 87504160 | ||||||
chr7:87504173 | T | C | 1 | a0001c0004t0020 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 70 | chr7 | 87504173 | ||||||
chr7:87504222 | A | G | 3 | a0001c0001t0006 a0001c0001t0021 a0001c0003t0006 |
9 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*21T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 28/28 | 21 | chr7 | 87504222 | ||||||
chr7:87600185 | T | C | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
5_prime_UTR_variant | MODIFIER | c.-1A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/28 | 1 | chr7 | 87600185 | ||||||
chr7:87600791 | T | C | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG03540.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-43A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/28 | 607 | chr7 | 87600791 | ||||||
chr7:87600877 | A | G | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(8): Show |
33 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/28 | 693 | chr7 | 87600877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87504535 | A | G | 25 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0179 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.3637-86T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504535 | |||||||
chr7:87504536 | T | C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0111 others(30): Show |
33 | HG00639.hp2 HG00738.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.3637-87A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504536 | |||||||
chr7:87504547 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3637-98C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504547 | |||||||
chr7:87504568 | G | A | 3 | a0001c0006t0001g0235 a0002c0002t0001g0006 a0002c0002t0001g0160 |
4 | NA18970.hp1 NA18982.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.3637-119C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504568 | |||||||
chr7:87504580 | G | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3637-131C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504580 | |||||||
chr7:87504584 | A | G | 4 | a0001c0001t0001g0266 a0001c0001t0009g0267 a0001c0022t0001g0268 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3637-135T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504584 | |||||||
chr7:87504601 | T | C | 4 | a0001c0001t0001g0297 a0001c0001t0001g0299 a0001c0001t0019g0311 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3637-152A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504601 | |||||||
chr7:87504601 | T | G | 2 | a0001c0001t0001g0065 a0001c0018t0017g0039 |
2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3637-152A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504601 | |||||||
chr7:87504616 | T | C | 10 | a0001c0001t0001g0084 a0001c0001t0002g0337 a0001c0001t0002g0338 others(7): Show |
10 | HG01243.hp2 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.3637-167A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504616 | |||||||
chr7:87504617 | A | G | 2 | a0001c0001t0001g0292 a0001c0003t0001g0164 |
2 | HG01928.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3637-168T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504617 | |||||||
chr7:87504631 | C | A | 31 | a0001c0001t0001g0117 a0001c0001t0001g0191 a0001c0001t0001g0193 others(28): Show |
32 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3637-182G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504631 | |||||||
chr7:87504661 | T | C | 1 | a0001c0001t0004g0329 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3637-212A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504661 | |||||||
chr7:87504666 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0002c0002t0002g0121 others(1): Show |
4 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3637-217A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504666 | |||||||
chr7:87504669 | G | T | 3 | a0001c0001t0001g0091 a0002c0002t0002g0121 a0011c0029t0002g0130 |
3 | HG00735.hp1 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3637-220C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504669 | |||||||
chr7:87504673 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0201 others(3): Show |
6 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3637-224A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504673 | |||||||
chr7:87504677 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0091 others(54): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3637-228A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504677 | |||||||
chr7:87504808 | G | GA | 19 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(16): Show |
19 | HG01175.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.3637-360dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504808 | |||||||
chr7:87504808 | GA | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0250 others(16): Show |
21 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3637-360delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504808 | |||||||
chr7:87504819 | A | AT | 11 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0068 others(8): Show |
11 | HG02258.hp1 HG02895.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.3637-371_3637-370i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504819 | |||||||
chr7:87504819 | A | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0250 others(11): Show |
16 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.3637-370T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504819 | |||||||
chr7:87504978 | T | A | 1 | a0001c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3637-529A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87504978 | |||||||
chr7:87505017 | G | A | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3637-568C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505017 | |||||||
chr7:87505219 | C | G | 34 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3636+678G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505219 | |||||||
chr7:87505243 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3636+654C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505243 | |||||||
chr7:87505504 | T | C | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3636+393A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505504 | |||||||
chr7:87505639 | T | C | 1 | a0016c0015t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3636+258A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505639 | |||||||
chr7:87505869 | T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3636+28A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 27/27 | chr7 | 87505869 | |||||||
chr7:87506164 | A | G | 5 | a0001c0001t0003g0037 a0001c0001t0008g0097 a0001c0001t0008g0098 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3490-121T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506164 | |||||||
chr7:87506550 | AT | A | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-508delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506550 | |||||||
chr7:87506553 | A | T | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-510T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506553 | |||||||
chr7:87506554 | A | T | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-511T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506554 | |||||||
chr7:87506557 | T | A | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-514A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506557 | |||||||
chr7:87506867 | C | T | 3 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0013c0026t0014g0010 |
3 | HG02280.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3490-824G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87506867 | |||||||
chr7:87507016 | T | C | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-973A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507016 | |||||||
chr7:87507261 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3490-1218G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507261 | |||||||
chr7:87507355 | T | C | 14 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0088 others(11): Show |
14 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3490-1312A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507355 | |||||||
chr7:87507392 | G | A | 8 | a0001c0001t0004g0100 a0001c0001t0005g0034 a0003c0007t0001g0102 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3490-1349C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507392 | |||||||
chr7:87507441 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3490-1398G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507441 | |||||||
chr7:87507699 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0091 others(65): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3489+1576G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507699 | |||||||
chr7:87507702 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0056 others(191): Show |
197 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.3489+1573G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507702 | |||||||
chr7:87507995 | AG | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0091 others(65): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3489+1279delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87507995 | |||||||
chr7:87508142 | T | G | 8 | a0001c0001t0001g0065 a0001c0001t0001g0250 a0001c0001t0003g0036 others(5): Show |
8 | HG01081.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3489+1133A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508142 | |||||||
chr7:87508145 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0091 others(65): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3489+1130C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508145 | |||||||
chr7:87508162 | G | A | 4 | a0001c0001t0001g0295 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG01516.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.3489+1113C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508162 | |||||||
chr7:87508446 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3489+829A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508446 | |||||||
chr7:87508734 | A | G | 1 | a0002c0002t0001g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3489+541T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508734 | |||||||
chr7:87508870 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(336): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.3489+405T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508870 | |||||||
chr7:87508911 | G | C | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3489+364C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87508911 | |||||||
chr7:87509193 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3489+82C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509193 | |||||||
chr7:87509195 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(235): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.3489+80C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509195 | |||||||
chr7:87509216 | A | C | 106 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(103): Show |
106 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3489+59T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 26/27 | chr7 | 87509216 | |||||||
chr7:87509638 | A | G | 7 | a0001c0001t0005g0034 a0003c0007t0001g0102 a0003c0007t0001g0258 others(4): Show |
7 | HG00639.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3283-157T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87509638 | |||||||
chr7:87509681 | T | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3283-200A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87509681 | |||||||
chr7:87510000 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(111): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.3283-519T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510000 | |||||||
chr7:87510141 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3283-660A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510141 | |||||||
chr7:87510737 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3283-1256A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510737 | |||||||
chr7:87510804 | A | C | 1 | a0001c0001t0002g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3283-1323T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510804 | |||||||
chr7:87510856 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3283-1375C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510856 | |||||||
chr7:87510859 | G | A | 8 | a0001c0001t0001g0065 a0001c0001t0001g0250 a0001c0001t0003g0036 others(5): Show |
8 | HG01081.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3283-1378C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87510859 | |||||||
chr7:87511027 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0190 a0001c0001t0001g0208 |
3 | HG02056.hp2 HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3283-1546G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511027 | |||||||
chr7:87511395 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3283-1914C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511395 | |||||||
chr7:87511435 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3283-1954A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511435 | |||||||
chr7:87511465 | T | C | 1 | a0002c0002t0001g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3283-1984A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511465 | |||||||
chr7:87511492 | A | G | 52 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0123 others(49): Show |
54 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.3283-2011T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511492 | |||||||
chr7:87511512 | A | T | 1 | a0016c0015t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3283-2031T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511512 | |||||||
chr7:87511823 | G | C | 2 | a0001c0003t0006g0062 a0001c0003t0009g0113 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3283-2342C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511823 | |||||||
chr7:87511858 | G | C | 113 | a0001c0001t0001g0051 a0001c0001t0001g0084 a0001c0001t0001g0087 others(110): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3283-2377C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87511858 | |||||||
chr7:87512181 | A | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(238): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.3283-2700T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512181 | |||||||
chr7:87512182 | A | C | 2 | a0001c0001t0019g0311 a0001c0004t0002g0270 |
2 | NA18964.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3283-2701T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512182 | |||||||
chr7:87512190 | A | T | 1 | a0001c0001t0008g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3283-2709T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512190 | |||||||
chr7:87512190 | AT | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(118): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.3283-2710delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512190 | |||||||
chr7:87512236 | T | G | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3283-2755A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512236 | |||||||
chr7:87512354 | G | A | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3283-2873C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512354 | |||||||
chr7:87512435 | C | T | 110 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(107): Show |
110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.3282+2796G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512435 | |||||||
chr7:87512498 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(250): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3282+2733A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512498 | |||||||
chr7:87512556 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3282+2675G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512556 | |||||||
chr7:87512636 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3282+2595T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512636 | |||||||
chr7:87512673 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0031 |
2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.3282+2558C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512673 | |||||||
chr7:87512769 | T | G | 1 | a0001c0001t0002g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3282+2462A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512769 | |||||||
chr7:87512868 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3282+2363C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512868 | |||||||
chr7:87512895 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3282+2336G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512895 | |||||||
chr7:87512939 | A | C | 1 | a0001c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3282+2292T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87512939 | |||||||
chr7:87513133 | G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3282+2098C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513133 | |||||||
chr7:87513158 | G | T | 8 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0088 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3282+2073C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513158 | |||||||
chr7:87513243 | C | CCTTTT | 254 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(251): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3282+1987_3282+198 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513243 | |||||||
chr7:87513510 | G | C | 4 | a0001c0004t0005g0013 a0001c0004t0005g0014 a0001c0004t0005g0016 others(1): Show |
4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.3282+1721C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513510 | |||||||
chr7:87513658 | G | A | 1 | a0003c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3282+1573C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513658 | |||||||
chr7:87513837 | T | C | 103 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(100): Show |
103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.3282+1394A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513837 | |||||||
chr7:87513932 | G | A | 1 | a0001c0004t0005g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3282+1299C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513932 | |||||||
chr7:87513939 | T | A | 8 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0088 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3282+1292A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513939 | |||||||
chr7:87513959 | T | C | 122 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(119): Show |
122 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.3282+1272A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87513959 | |||||||
chr7:87514006 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3282+1225T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514006 | |||||||
chr7:87514188 | C | T | 120 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(117): Show |
120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.3282+1043G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514188 | |||||||
chr7:87514225 | T | C | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3282+1006A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514225 | |||||||
chr7:87514425 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3282+806A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514425 | |||||||
chr7:87514707 | T | C | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3282+524A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514707 | |||||||
chr7:87514877 | C | G | 3 | a0001c0003t0001g0164 a0001c0003t0001g0318 a0001c0003t0002g0255 |
3 | HG00558.hp2 HG00609.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3282+354G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87514877 | |||||||
chr7:87515097 | G | C | 53 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0068 others(50): Show |
53 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.3282+134C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 25/27 | chr7 | 87515097 | |||||||
chr7:87515500 | G | C | 117 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(114): Show |
117 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.3085-72C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515500 | |||||||
chr7:87515543 | C | T | 1 | a0003c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3085-115G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515543 | |||||||
chr7:87515701 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3085-273C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515701 | |||||||
chr7:87515817 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.3085-389C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515817 | |||||||
chr7:87515831 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3085-403T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87515831 | |||||||
chr7:87516018 | C | T | 1 | a0002c0002t0001g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3084+491G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516018 | |||||||
chr7:87516108 | T | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3084+401A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516108 | |||||||
chr7:87516119 | G | A | 2 | a0001c0003t0006g0062 a0001c0003t0009g0113 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3084+390C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516119 | |||||||
chr7:87516167 | G | A | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.3084+342C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516167 | |||||||
chr7:87516231 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3084+278C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516231 | |||||||
chr7:87516493 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | NA18960.hp1 NA19011.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3084+16C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 24/27 | chr7 | 87516493 | |||||||
chr7:87516728 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2928-63G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516728 | |||||||
chr7:87516731 | C | CT | 12 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0208 others(9): Show |
12 | HG00544.hp1 HG01358.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2928-67dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTT | 31 | a0001c0003t0001g0109 a0001c0003t0001g0161 a0001c0003t0001g0164 others(28): Show |
31 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2928-70_2928-67dup others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTT | 8 | a0001c0001t0008g0098 a0001c0003t0001g0156 a0001c0003t0001g0157 others(5): Show |
8 | HG02083.hp1 HG02135.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2928-71_2928-67dup others(5): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT | 7 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(4): Show |
7 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2928-73_2928-67dup others(7): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0010g0035 a0001c0004t0002g0054 a0001c0004t0002g0134 |
3 | HG02129.hp2 HG03834.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2928-83_2928-67dup others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(11): Show |
29 | a0001c0001t0001g0056 a0001c0001t0001g0068 a0001c0001t0001g0073 others(26): Show |
29 | HG00639.hp2 HG01496.hp2 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.2928-84_2928-67dup others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(12): Show |
23 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0074 others(20): Show |
23 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.2928-85_2928-67dup others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0004t0002g0048 others(6): Show |
9 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2928-86_2928-67dup others(20): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(14): Show |
2 | a0001c0004t0005g0019 a0008c0013t0001g0262 |
2 | HG00423.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2928-87_2928-67dup others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | C | CTTTTTTT others(17): Show |
1 | a0001c0004t0005g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2928-67_2928-66ins others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516731 | CTT | C | 51 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(48): Show |
51 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2928-68_2928-67del others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516731 | |||||||
chr7:87516956 | C | T | 1 | a0001c0003t0002g0229 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2928-291G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516956 | |||||||
chr7:87516965 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2928-300C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87516965 | |||||||
chr7:87517326 | A | G | 1 | a0001c0004t0012g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2928-661T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517326 | |||||||
chr7:87517364 | T | TTC | 60 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(57): Show |
60 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2928-701_2928-700d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517364 | |||||||
chr7:87517513 | GATCCACT others(7): Show |
G | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2928-862_2928-849d others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517513 | |||||||
chr7:87517606 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2928-941C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517606 | |||||||
chr7:87517688 | G | C | 1 | a0003c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2928-1023C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517688 | |||||||
chr7:87517831 | T | A | 55 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(52): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2928-1166A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517831 | |||||||
chr7:87517832 | GT | G | 55 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(52): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2928-1168delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87517832 | |||||||
chr7:87518241 | A | G | 2 | a0002c0002t0001g0129 a0002c0002t0001g0155 |
2 | HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2927+1085T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518241 | |||||||
chr7:87518303 | T | C | 1 | a0003c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2927+1023A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518303 | |||||||
chr7:87518450 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2927+876A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518450 | |||||||
chr7:87518539 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2927+787A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518539 | |||||||
chr7:87518658 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2927+668A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518658 | |||||||
chr7:87518887 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2927+439T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518887 | |||||||
chr7:87518949 | G | T | 60 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(57): Show |
60 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.2927+377C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518949 | |||||||
chr7:87518975 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2927+351A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87518975 | |||||||
chr7:87519012 | C | T | 55 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(52): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2927+314G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519012 | |||||||
chr7:87519081 | C | T | 1 | a0002c0002t0001g0321 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2927+245G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519081 | |||||||
chr7:87519171 | T | C | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2927+155A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 23/27 | chr7 | 87519171 | |||||||
chr7:87519596 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787-130C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519596 | |||||||
chr7:87519622 | G | A | 4 | a0001c0003t0001g0222 a0001c0003t0001g0224 a0001c0003t0001g0225 others(1): Show |
4 | HG01952.hp2 HG02148.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787-156C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519622 | |||||||
chr7:87519920 | AC | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2787-455delG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519920 | |||||||
chr7:87519922 | T | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2787-456A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87519922 | |||||||
chr7:87520008 | G | A | 1 | a0001c0005t0005g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2787-542C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520008 | |||||||
chr7:87520217 | A | AT | 55 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(52): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.2786+558dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520217 | |||||||
chr7:87520606 | C | T | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.2786+170G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 22/27 | chr7 | 87520606 | |||||||
chr7:87521167 | C | T | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-291G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521167 | |||||||
chr7:87521288 | C | T | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-412G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521288 | |||||||
chr7:87521407 | G | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2686-531C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521407 | |||||||
chr7:87521417 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2686-541C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521417 | |||||||
chr7:87521458 | G | A | 115 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(112): Show |
115 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2686-582C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521458 | |||||||
chr7:87521570 | A | G | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2686-694T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521570 | |||||||
chr7:87521621 | G | A | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-745C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521621 | |||||||
chr7:87521667 | G | A | 1 | a0001c0003t0002g0255 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2686-791C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521667 | |||||||
chr7:87521774 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(151): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2686-898A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521774 | |||||||
chr7:87521901 | C | T | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-1025G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87521901 | |||||||
chr7:87522067 | G | A | 3 | a0002c0002t0001g0154 a0002c0002t0001g0163 a0002c0002t0001g0168 |
3 | HG01167.hp2 HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2686-1191C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522067 | |||||||
chr7:87522090 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2686-1214G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522090 | |||||||
chr7:87522208 | C | G | 172 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(169): Show |
172 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.2686-1332G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522208 | |||||||
chr7:87522342 | C | T | 155 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(152): Show |
155 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2686-1466G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522342 | |||||||
chr7:87522368 | G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2686-1492C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522368 | |||||||
chr7:87522477 | C | T | 6 | a0001c0001t0007g0078 a0001c0005t0001g0131 a0001c0005t0001g0276 others(3): Show |
7 | HG00280.hp2 HG00323.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2686-1601G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522477 | |||||||
chr7:87522530 | G | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-1654C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522530 | |||||||
chr7:87522729 | A | G | 53 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-1853T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522729 | |||||||
chr7:87522748 | CT | C | 5 | a0001c0001t0001g0084 a0001c0001t0004g0049 a0001c0004t0012g0132 others(2): Show |
5 | HG01243.hp2 HG03209.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-1873delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522748 | |||||||
chr7:87522756 | TA | T | 51 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0068 others(48): Show |
51 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.2686-1881delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522756 | |||||||
chr7:87522757 | A | T | 53 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0256 others(50): Show |
53 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-1881T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522757 | |||||||
chr7:87522787 | A | G | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-1911T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87522787 | |||||||
chr7:87523022 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2686-2146A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523022 | |||||||
chr7:87523127 | G | T | 1 | a0001c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2686-2251C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523127 | |||||||
chr7:87523195 | G | A | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-2319C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523195 | |||||||
chr7:87523214 | G | A | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2686-2338C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523214 | |||||||
chr7:87523258 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2686-2382T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523258 | |||||||
chr7:87523307 | T | A | 50 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2686-2431A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523307 | |||||||
chr7:87523311 | G | A | 1 | a0001c0003t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2686-2435C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523311 | |||||||
chr7:87523339 | A | G | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2686-2463T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523339 | |||||||
chr7:87523474 | C | A | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-2598G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523474 | |||||||
chr7:87523551 | G | A | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2686-2675C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523551 | |||||||
chr7:87523563 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2686-2687T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523563 | |||||||
chr7:87523570 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2686-2694G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523570 | |||||||
chr7:87523711 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2686-2835G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523711 | |||||||
chr7:87523782 | C | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2686-2906G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523782 | |||||||
chr7:87523789 | C | A | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-2913G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523789 | |||||||
chr7:87523790 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2686-2914C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523790 | |||||||
chr7:87523821 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-2945A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523821 | |||||||
chr7:87523844 | G | A | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-2968C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523844 | |||||||
chr7:87523863 | A | G | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2686-2987T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523863 | |||||||
chr7:87523900 | C | T | 53 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2686-3024G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87523900 | |||||||
chr7:87524191 | AAC | A | 5 | a0002c0002t0001g0006 a0002c0002t0001g0148 a0002c0002t0001g0160 others(2): Show |
6 | NA18970.hp1 NA18973.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.2686-3317_2686-331 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524191 | |||||||
chr7:87524269 | A | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2686-3393T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524269 | |||||||
chr7:87524379 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2686-3503A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524379 | |||||||
chr7:87524555 | AG | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(79): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2686-3680delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524555 | |||||||
chr7:87524599 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2686-3723C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524599 | |||||||
chr7:87524701 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2686-3825C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524701 | |||||||
chr7:87524819 | C | G | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2686-3943G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524819 | |||||||
chr7:87524836 | T | C | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-3960A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87524836 | |||||||
chr7:87525041 | GT | G | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2686-4166delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525041 | |||||||
chr7:87525330 | A | G | 50 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2686-4454T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525330 | |||||||
chr7:87525438 | A | G | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2686-4562T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525438 | |||||||
chr7:87525696 | G | A | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-4820C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87525696 | |||||||
chr7:87526043 | T | A | 7 | a0002c0002t0001g0147 a0002c0002t0001g0169 a0002c0002t0001g0325 others(4): Show |
7 | NA18941.hp2 NA18949.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.2686-5167A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526043 | |||||||
chr7:87526164 | C | CT | 55 | a0001c0001t0001g0087 a0001c0001t0001g0179 a0001c0001t0001g0180 others(52): Show |
55 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2685+5129dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526164 | |||||||
chr7:87526164 | CT | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0101 others(20): Show |
26 | HG00280.hp1 HG00323.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.2685+5129delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526164 | |||||||
chr7:87526240 | T | C | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2685+5054A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526240 | |||||||
chr7:87526279 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(79): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2685+5015C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526279 | |||||||
chr7:87526461 | G | A | 1 | a0001c0004t0002g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2685+4833C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526461 | |||||||
chr7:87526618 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685+4676T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526618 | |||||||
chr7:87526666 | A | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2685+4628T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526666 | |||||||
chr7:87526688 | G | A | 2 | a0001c0001t0001g0317 a0003c0007t0001g0102 |
2 | HG02647.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2685+4606C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526688 | |||||||
chr7:87526693 | T | C | 4 | a0001c0004t0005g0013 a0001c0004t0005g0014 a0001c0004t0005g0016 others(1): Show |
4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+4601A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526693 | |||||||
chr7:87526720 | C | A | 3 | a0001c0001t0001g0084 a0001c0001t0004g0049 a0001c0001t0005g0034 |
3 | HG01243.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+4574G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526720 | |||||||
chr7:87526875 | G | T | 17 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(14): Show |
17 | HG00738.hp2 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2685+4419C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526875 | |||||||
chr7:87526985 | G | A | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2685+4309C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87526985 | |||||||
chr7:87527063 | A | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2685+4231T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527063 | |||||||
chr7:87527098 | C | T | 1 | a0001c0001t0018g0281 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2685+4196G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527098 | |||||||
chr7:87527131 | T | C | 1 | a0002c0010t0003g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2685+4163A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527131 | |||||||
chr7:87527198 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+4096C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527198 | |||||||
chr7:87527215 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2685+4079A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527215 | |||||||
chr7:87527240 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2685+4054G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527240 | |||||||
chr7:87527326 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2685+3968A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527326 | |||||||
chr7:87527445 | A | G | 1 | a0002c0002t0011g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2685+3849T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527445 | |||||||
chr7:87527733 | T | C | 2 | a0001c0001t0001g0207 a0001c0005t0003g0003 |
3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2685+3561A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527733 | |||||||
chr7:87527735 | G | A | 171 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(168): Show |
171 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.2685+3559C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527735 | |||||||
chr7:87527904 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685+3390A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527904 | |||||||
chr7:87527978 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0004g0049 a0002c0002t0001g0136 |
3 | HG01243.hp2 HG02056.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2685+3316G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87527978 | |||||||
chr7:87528076 | G | C | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2685+3218C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528076 | |||||||
chr7:87528150 | C | G | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2685+3144G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528150 | |||||||
chr7:87528181 | G | C | 1 | a0001c0005t0001g0126 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2685+3113C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528181 | |||||||
chr7:87528267 | A | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(262): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2685+3027T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528267 | |||||||
chr7:87528284 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2685+3010C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528284 | |||||||
chr7:87528313 | T | C | 53 | a0001c0001t0001g0084 a0001c0001t0001g0123 a0001c0001t0001g0125 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2685+2981A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528313 | |||||||
chr7:87528328 | T | A | 56 | a0001c0001t0001g0084 a0001c0001t0001g0123 a0001c0001t0001g0125 others(53): Show |
56 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.2685+2966A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528328 | |||||||
chr7:87528390 | C | T | 100 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2685+2904G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528390 | |||||||
chr7:87528439 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2685+2855T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528439 | |||||||
chr7:87528869 | G | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(262): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2685+2425C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87528869 | |||||||
chr7:87529084 | A | T | 1 | a0001c0003t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2685+2210T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529084 | |||||||
chr7:87529596 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2685+1698A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529596 | |||||||
chr7:87529736 | T | G | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2685+1558A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529736 | |||||||
chr7:87529934 | G | A | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2685+1360C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87529934 | |||||||
chr7:87530012 | G | T | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG00408.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+1282C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530012 | |||||||
chr7:87530203 | A | C | 3 | a0001c0001t0004g0182 a0001c0001t0004g0259 a0001c0001t0004g0264 |
3 | HG02109.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2685+1091T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530203 | |||||||
chr7:87530570 | G | A | 3 | a0001c0003t0001g0164 a0001c0003t0001g0318 a0001c0003t0002g0255 |
3 | HG00558.hp2 HG00609.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2685+724C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530570 | |||||||
chr7:87530757 | A | G | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2685+537T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530757 | |||||||
chr7:87530790 | A | AAAGAAAG others(1): Show |
26 | a0001c0001t0001g0203 a0001c0001t0004g0100 a0002c0002t0001g0005 others(23): Show |
27 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.2685+496_2685+503d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530790 | A | AAAGAAAG others(9): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2685+488_2685+503d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530790 | A | C | 1 | a0002c0009t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2685+504T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530790 | AAAGAAAG others(1): Show |
A | 13 | a0001c0001t0001g0084 a0001c0001t0001g0186 a0001c0001t0019g0311 others(10): Show |
13 | HG00609.hp2 HG01243.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2685+496_2685+503d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530790 | AAAGAAAG others(9): Show |
A | 5 | a0001c0001t0001g0181 a0001c0001t0008g0055 a0001c0003t0001g0109 others(2): Show |
5 | HG01952.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685+488_2685+503d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530790 | AAAGAAAG others(17): Show |
A | 2 | a0001c0004t0002g0069 a0001c0004t0002g0072 |
2 | HG01123.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2685+480_2685+503d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530790 | |||||||
chr7:87530796 | A | AGCAAGAA others(1): Show |
5 | a0001c0001t0003g0002 a0001c0001t0003g0027 a0001c0001t0003g0029 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+497_2685+498i others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530796 | |||||||
chr7:87530804 | A | C | 3 | a0001c0001t0003g0024 a0001c0001t0003g0031 a0001c0001t0010g0026 |
3 | HG00280.hp1 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2685+490T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530804 | |||||||
chr7:87530818 | AAAGCAAG others(5): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2685+464_2685+475d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530818 | |||||||
chr7:87530818 | AAAGCAAG others(13): Show |
A | 1 | a0001c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2685+456_2685+475d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530818 | |||||||
chr7:87530822 | CAAGAAAG others(13): Show |
C | 55 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(52): Show |
55 | HG00423.hp2 HG01358.hp2 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.2685+452_2685+471d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530822 | |||||||
chr7:87530822 | CAAGAAAG others(17): Show |
C | 49 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2685+448_2685+471d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530822 | |||||||
chr7:87530826 | AAAGCAAG others(5): Show |
A | 1 | a0001c0004t0002g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2685+456_2685+467d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530826 | |||||||
chr7:87530830 | C | CAAGA | 6 | a0001c0001t0001g0065 a0001c0001t0004g0049 a0001c0001t0004g0182 others(3): Show |
6 | HG01081.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+460_2685+463d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | |||||||
chr7:87530830 | CAAGAAAG others(5): Show |
C | 27 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(24): Show |
27 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.2685+452_2685+463d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | |||||||
chr7:87530830 | CAAGAAAG others(9): Show |
C | 1 | a0002c0002t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2685+448_2685+463d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | |||||||
chr7:87530830 | CAAGAAAG others(13): Show |
C | 3 | a0006c0011t0001g0092 a0006c0011t0001g0093 a0006c0011t0001g0094 |
3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2685+444_2685+463d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | |||||||
chr7:87530830 | CAAGAAAG others(17): Show |
C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685+440_2685+463d others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530830 | |||||||
chr7:87530834 | AAAGC | A | 8 | a0001c0003t0001g0156 a0001c0003t0001g0224 a0001c0003t0001g0225 others(5): Show |
8 | HG00639.hp1 HG02083.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2685+456_2685+459d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530834 | |||||||
chr7:87530838 | C | A | 16 | a0001c0001t0001g0065 a0001c0001t0001g0193 a0001c0001t0001g0213 others(13): Show |
17 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2685+456G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGA | 12 | a0001c0001t0001g0119 a0001c0001t0001g0191 a0001c0001t0003g0024 others(9): Show |
15 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2685+452_2685+455d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(1): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0091 others(26): Show |
29 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.2685+448_2685+455d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(5): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0192 others(10): Show |
14 | HG00280.hp2 HG00738.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2685+444_2685+455d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(9): Show |
6 | a0001c0001t0001g0118 a0001c0001t0001g0214 a0001c0001t0002g0274 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2685+440_2685+455d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(13): Show |
4 | a0001c0001t0001g0108 a0001c0001t0001g0206 a0001c0001t0001g0250 others(1): Show |
4 | HG01261.hp2 HG03098.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685+436_2685+455d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(5): Show |
13 | a0002c0002t0001g0135 a0002c0002t0001g0136 a0002c0002t0001g0142 others(10): Show |
13 | HG00558.hp1 HG01257.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(9): Show |
8 | a0001c0001t0001g0112 a0001c0001t0002g0337 a0001c0005t0003g0003 others(5): Show |
10 | HG00544.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(13): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0207 a0002c0002t0001g0105 others(1): Show |
4 | HG01433.hp2 HG03490.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2685+455_2685+456i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(17): Show |
1 | a0002c0002t0001g0160 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2685+455_2685+456i others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(13): Show |
1 | a0001c0001t0001g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2685+455_2685+456i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | C | CAAGAAAG others(21): Show |
1 | a0001c0001t0002g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2685+455_2685+456i others(30): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530838 | CAAGA | C | 9 | a0001c0003t0006g0062 a0001c0003t0006g0081 a0001c0003t0009g0113 others(6): Show |
9 | HG00741.hp2 HG01167.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2685+452_2685+455d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530838 | |||||||
chr7:87530842 | A | AAAGC | 15 | a0001c0006t0004g0103 a0002c0002t0001g0147 a0002c0002t0001g0168 others(12): Show |
15 | HG01192.hp2 HG01258.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.2685+451_2685+452i others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530842 | |||||||
chr7:87530846 | A | C | 1 | a0001c0006t0004g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2685+448T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530846 | |||||||
chr7:87530850 | A | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2685+444T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530850 | |||||||
chr7:87530889 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2685+405T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87530889 | |||||||
chr7:87531245 | A | G | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2685+49T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 21/27 | chr7 | 87531245 | |||||||
chr7:87531733 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-236A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531733 | |||||||
chr7:87531983 | A | T | 1 | a0001c0003t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2482-486T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531983 | |||||||
chr7:87531992 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2482-495C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87531992 | |||||||
chr7:87532204 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-707A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532204 | |||||||
chr7:87532267 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-770A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532267 | |||||||
chr7:87532480 | C | T | 2 | a0004c0008t0001g0215 a0004c0008t0001g0217 |
2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2482-983G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532480 | |||||||
chr7:87532561 | A | T | 1 | a0002c0002t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2482-1064T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532561 | |||||||
chr7:87532716 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2482-1219G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532716 | |||||||
chr7:87532751 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2482-1254A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532751 | |||||||
chr7:87532928 | C | G | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2482-1431G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532928 | |||||||
chr7:87532967 | G | A | 8 | a0001c0004t0001g0043 a0001c0004t0002g0041 a0001c0004t0002g0044 others(5): Show |
8 | HG01358.hp2 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-1470C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532967 | |||||||
chr7:87532986 | C | A | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2482-1489G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87532986 | |||||||
chr7:87533012 | A | G | 1 | a0001c0003t0001g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2482-1515T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533012 | |||||||
chr7:87533025 | A | G | 103 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(100): Show |
103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2482-1528T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533025 | |||||||
chr7:87533514 | C | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-2017G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533514 | |||||||
chr7:87533571 | T | C | 5 | a0002c0002t0001g0127 a0002c0002t0001g0135 a0002c0002t0001g0165 others(2): Show |
5 | HG00558.hp1 HG02015.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.2482-2074A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533571 | |||||||
chr7:87533700 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2482-2203A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533700 | |||||||
chr7:87533733 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(252): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2482-2236G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533733 | |||||||
chr7:87533809 | T | C | 8 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(5): Show |
9 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-2312A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533809 | |||||||
chr7:87533847 | T | C | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-2350A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533847 | |||||||
chr7:87533964 | G | C | 1 | a0002c0002t0001g0171 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2482-2467C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87533964 | |||||||
chr7:87534004 | C | T | 3 | a0006c0011t0001g0092 a0006c0011t0001g0093 a0006c0011t0001g0094 |
3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2481+2454G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534004 | |||||||
chr7:87534007 | C | A | 1 | a0001c0003t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2481+2451G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534007 | |||||||
chr7:87534297 | T | C | 2 | a0001c0003t0001g0233 a0001c0003t0002g0227 |
2 | NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2481+2161A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534297 | |||||||
chr7:87534411 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0260 a0001c0001t0001g0305 |
3 | HG02145.hp2 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2481+2047A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534411 | |||||||
chr7:87534434 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2481+2024C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534434 | |||||||
chr7:87534913 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2481+1545A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534913 | |||||||
chr7:87534915 | T | C | 5 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+1543A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534915 | |||||||
chr7:87534917 | T | TA | 35 | a0001c0001t0001g0091 a0001c0001t0001g0118 a0001c0001t0001g0188 others(32): Show |
35 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2481+1540dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | T | TAA | 47 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0125 others(44): Show |
47 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2481+1539_2481+154 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | T | TAAA | 9 | a0001c0001t0001g0283 a0001c0001t0001g0287 a0001c0001t0001g0291 others(6): Show |
9 | HG01123.hp1 HG01346.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.2481+1538_2481+154 others(7): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | T | TAAAAA | 72 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(69): Show |
72 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2481+1536_2481+154 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | T | TAAAAAA | 20 | a0001c0001t0006g0066 a0001c0001t0008g0055 a0001c0003t0001g0156 others(17): Show |
20 | HG00423.hp2 HG01123.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.2481+1535_2481+154 others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2481+1530_2481+154 others(15): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534917 | TA | T | 9 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(6): Show |
10 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+1540delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534917 | |||||||
chr7:87534926 | A | AAC | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(3): Show |
6 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2481+1531_2481+153 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534926 | |||||||
chr7:87534945 | A | AT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(72): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2481+1512dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534945 | |||||||
chr7:87534945 | A | ATT | 7 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
7 | HG00408.hp2 HG00597.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.2481+1511_2481+151 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534945 | |||||||
chr7:87534954 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2481+1504A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87534954 | |||||||
chr7:87535015 | A | G | 5 | a0002c0002t0001g0152 a0002c0002t0001g0158 a0002c0002t0001g0275 others(2): Show |
5 | HG02071.hp2 NA18964.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2481+1443T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535015 | |||||||
chr7:87535033 | A | C | 3 | a0005c0012t0001g0271 a0005c0012t0001g0273 a0005c0017t0002g0272 |
3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2481+1425T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535033 | |||||||
chr7:87535167 | G | A | 50 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2481+1291C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535167 | |||||||
chr7:87535261 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2481+1197A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535261 | |||||||
chr7:87535312 | T | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+1146A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535312 | |||||||
chr7:87535338 | A | AT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0060 others(78): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2481+1119dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | |||||||
chr7:87535338 | A | ATT | 100 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0068 others(97): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2481+1118_2481+111 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | |||||||
chr7:87535338 | AT | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0099 others(23): Show |
29 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2481+1119delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535338 | |||||||
chr7:87535387 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2481+1071A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535387 | |||||||
chr7:87535440 | C | A | 103 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(100): Show |
103 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2481+1018G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535440 | |||||||
chr7:87535520 | G | GA | 165 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(162): Show |
165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2481+937_2481+938i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535520 | |||||||
chr7:87535539 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2481+919G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535539 | |||||||
chr7:87535576 | T | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(252): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2481+882A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535576 | |||||||
chr7:87535654 | C | T | 1 | a0005c0017t0002g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2481+804G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535654 | |||||||
chr7:87535670 | A | G | 165 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(162): Show |
165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2481+788T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535670 | |||||||
chr7:87535735 | G | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2481+723C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535735 | |||||||
chr7:87535838 | C | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2481+620G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87535838 | |||||||
chr7:87536090 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2481+368A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536090 | |||||||
chr7:87536095 | C | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2481+363G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536095 | |||||||
chr7:87536316 | G | A | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2481+142C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536316 | |||||||
chr7:87536372 | C | T | 1 | a0003c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2481+86G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536372 | |||||||
chr7:87536385 | G | T | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+73C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536385 | |||||||
chr7:87536418 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+40C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536418 | |||||||
chr7:87536434 | C | T | 50 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2481+24G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 20/27 | chr7 | 87536434 | |||||||
chr7:87536915 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2398-374C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87536915 | |||||||
chr7:87536966 | T | C | 2 | a0001c0003t0002g0244 a0001c0003t0002g0245 |
2 | HG00544.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2398-425A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87536966 | |||||||
chr7:87537031 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2398-490C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537031 | |||||||
chr7:87537133 | G | A | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2398-592C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537133 | |||||||
chr7:87537442 | G | T | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2398-901C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537442 | |||||||
chr7:87537504 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2398-963C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537504 | |||||||
chr7:87537552 | T | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2398-1011A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537552 | |||||||
chr7:87537665 | T | C | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2398-1124A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537665 | |||||||
chr7:87537688 | C | T | 62 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(59): Show |
62 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(59): Show |
intron_variant | MODIFIER | c.2398-1147G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537688 | |||||||
chr7:87537956 | T | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0027 a0001c0001t0010g0026 |
4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+1312A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537956 | |||||||
chr7:87537980 | C | T | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2397+1288G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87537980 | |||||||
chr7:87538393 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2397+875A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538393 | |||||||
chr7:87538586 | C | T | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2397+682G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538586 | |||||||
chr7:87538711 | C | T | 62 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(59): Show |
62 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(59): Show |
intron_variant | MODIFIER | c.2397+557G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538711 | |||||||
chr7:87538715 | T | C | 1 | a0001c0003t0002g0141 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2397+553A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538715 | |||||||
chr7:87538769 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2397+499A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538769 | |||||||
chr7:87538912 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2397+356G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87538912 | |||||||
chr7:87539139 | C | T | 6 | a0001c0004t0002g0047 a0001c0004t0002g0050 a0001c0004t0002g0054 others(3): Show |
6 | HG02129.hp2 NA18955.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2397+129G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539139 | |||||||
chr7:87539140 | G | A | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2397+128C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539140 | |||||||
chr7:87539212 | A | G | 4 | a0001c0001t0002g0216 a0001c0001t0002g0274 a0004c0008t0001g0187 others(1): Show |
4 | HG00738.hp1 HG01261.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+56T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 19/27 | chr7 | 87539212 | |||||||
chr7:87539433 | C | T | 334 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(331): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2320-88G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539433 | |||||||
chr7:87539721 | C | T | 64 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(61): Show |
64 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.2320-376G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539721 | |||||||
chr7:87539876 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2320-531C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87539876 | |||||||
chr7:87540040 | C | T | 32 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0283 others(29): Show |
32 | HG00140.hp1 HG00423.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.2320-695G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540040 | |||||||
chr7:87540079 | A | T | 2 | a0009c0030t0001g0242 a0009c0031t0002g0241 |
2 | NA18612.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2320-734T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540079 | |||||||
chr7:87540106 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2320-761A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540106 | |||||||
chr7:87540148 | T | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-803A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540148 | |||||||
chr7:87540353 | T | C | 52 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2319+1004A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540353 | |||||||
chr7:87540386 | A | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0173 |
3 | HG01070.hp2 HG01515.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2319+971T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540386 | |||||||
chr7:87540504 | G | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2319+853C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540504 | |||||||
chr7:87540567 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2319+790T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540567 | |||||||
chr7:87540701 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0060 others(79): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2319+656G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540701 | |||||||
chr7:87540847 | A | G | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2319+510T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87540847 | |||||||
chr7:87541189 | A | G | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2319+168T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 18/27 | chr7 | 87541189 | |||||||
chr7:87541491 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2212-27A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541491 | |||||||
chr7:87541576 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2212-112G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541576 | |||||||
chr7:87541836 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2212-372A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87541836 | |||||||
chr7:87542037 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2212-573A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542037 | |||||||
chr7:87542067 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2212-603C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542067 | |||||||
chr7:87542211 | T | C | 50 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2212-747A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542211 | |||||||
chr7:87542343 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(207): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2212-879A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542343 | |||||||
chr7:87542363 | A | G | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2212-899T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542363 | |||||||
chr7:87542387 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2212-923A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542387 | |||||||
chr7:87542544 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2212-1080G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542544 | |||||||
chr7:87542571 | C | T | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2212-1107G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542571 | |||||||
chr7:87542575 | T | C | 1 | a0002c0002t0001g0136 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2212-1111A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542575 | |||||||
chr7:87542658 | CT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(152): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2212-1195delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542658 | |||||||
chr7:87542737 | A | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(331): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2212-1273T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542737 | |||||||
chr7:87542816 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+1313A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542816 | |||||||
chr7:87542820 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2211+1309A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87542820 | |||||||
chr7:87543073 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2211+1056A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543073 | |||||||
chr7:87543105 | C | A | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02015.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.2211+1024G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543105 | |||||||
chr7:87543175 | T | A | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2211+954A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543175 | |||||||
chr7:87543180 | G | C | 1 | a0002c0002t0001g0275 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2211+949C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543180 | |||||||
chr7:87543249 | G | A | 9 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211+880C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543249 | |||||||
chr7:87543272 | C | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2211+857G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543272 | |||||||
chr7:87543282 | C | T | 67 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(64): Show |
67 | HG00423.hp2 HG01123.hp2 HG01192.hp1 others(64): Show |
intron_variant | MODIFIER | c.2211+847G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543282 | |||||||
chr7:87543340 | G | A | 1 | a0001c0004t0001g0043 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211+789C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543340 | |||||||
chr7:87543535 | C | T | 1 | a0001c0005t0001g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2211+594G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543535 | |||||||
chr7:87543565 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2211+564G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543565 | |||||||
chr7:87543583 | T | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2211+546A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543583 | |||||||
chr7:87543776 | A | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+353T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543776 | |||||||
chr7:87543786 | A | T | 5 | a0001c0001t0001g0295 a0001c0001t0001g0315 a0001c0001t0001g0316 others(2): Show |
5 | HG01123.hp1 HG01516.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+343T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543786 | |||||||
chr7:87543800 | A | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2211+329T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 17/27 | chr7 | 87543800 | |||||||
chr7:87544351 | A | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(149): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2065-76T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544351 | |||||||
chr7:87544489 | A | T | 1 | a0001c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2065-214T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544489 | |||||||
chr7:87544576 | T | G | 4 | a0001c0001t0006g0059 a0001c0001t0006g0061 a0001c0001t0006g0238 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+247A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544576 | |||||||
chr7:87544741 | C | T | 2 | a0001c0004t0005g0011 a0001c0004t0005g0012 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2064+82G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544741 | |||||||
chr7:87544750 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(212): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2064+73A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 16/27 | chr7 | 87544750 | |||||||
chr7:87545068 | A | G | 1 | a0001c0003t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1888-69T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545068 | |||||||
chr7:87545074 | G | A | 4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0004g0329 others(1): Show |
4 | HG00323.hp2 HG01106.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1888-75C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545074 | |||||||
chr7:87545094 | T | C | 1 | a0001c0004t0005g0019 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1888-95A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545094 | |||||||
chr7:87545144 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0001 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1888-155_1888-146d others(12): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545144 | |||||||
chr7:87545188 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(146): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1888-189G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545188 | |||||||
chr7:87545261 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1888-262G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545261 | |||||||
chr7:87545265 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1888-266G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545265 | |||||||
chr7:87545293 | A | G | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1888-294T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545293 | |||||||
chr7:87545477 | C | T | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1887+386G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545477 | |||||||
chr7:87545478 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1887+385C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545478 | |||||||
chr7:87545603 | A | G | 1 | a0001c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1887+260T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 15/27 | chr7 | 87545603 | |||||||
chr7:87546277 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1726-253G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546277 | |||||||
chr7:87546288 | A | G | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1726-264T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546288 | |||||||
chr7:87546303 | C | T | 2 | a0001c0001t0006g0058 a0001c0001t0006g0066 |
2 | HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1726-279G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546303 | |||||||
chr7:87546310 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(123): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1726-286G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546310 | |||||||
chr7:87546311 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1726-287C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546311 | |||||||
chr7:87546311 | G | T | 1 | a0001c0001t0011g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1726-287C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546311 | |||||||
chr7:87546474 | G | A | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(8): Show |
12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-450C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546474 | |||||||
chr7:87546488 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(138): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1726-464C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546488 | |||||||
chr7:87546562 | A | T | 2 | a0001c0001t0004g0049 a0001c0018t0017g0039 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1726-538T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546562 | |||||||
chr7:87546594 | AG | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(137): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1726-571delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546594 | |||||||
chr7:87546691 | A | G | 1 | a0002c0002t0002g0149 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1726-667T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546691 | |||||||
chr7:87546699 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-675A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546699 | |||||||
chr7:87546720 | C | G | 2 | a0002c0002t0001g0319 a0002c0002t0001g0320 |
2 | HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1726-696G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546720 | |||||||
chr7:87546765 | A | G | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1726-741T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546765 | |||||||
chr7:87546832 | A | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1726-808T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87546832 | |||||||
chr7:87547097 | T | C | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1726-1073A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547097 | |||||||
chr7:87547114 | C | T | 2 | a0001c0001t0019g0311 a0002c0010t0001g0090 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1726-1090G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547114 | |||||||
chr7:87547132 | C | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1726-1108G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547132 | |||||||
chr7:87547147 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1726-1123T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547147 | |||||||
chr7:87547155 | C | T | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1726-1131G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547155 | |||||||
chr7:87547321 | A | G | 4 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0088 others(1): Show |
4 | HG00639.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-1297T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547321 | |||||||
chr7:87547579 | A | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0239 a0001c0005t0001g0196 others(2): Show |
5 | HG01928.hp1 HG01981.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-1555T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547579 | |||||||
chr7:87547691 | G | A | 2 | a0005c0012t0001g0271 a0005c0012t0001g0273 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1725+1657C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547691 | |||||||
chr7:87547735 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1725+1613G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547735 | |||||||
chr7:87547805 | T | C | 51 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1725+1543A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547805 | |||||||
chr7:87547838 | G | A | 49 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1725+1510C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547838 | |||||||
chr7:87547850 | C | CA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(150): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1725+1497dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | |||||||
chr7:87547850 | C | CAA | 59 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0074 others(56): Show |
59 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1725+1496_1725+149 others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | |||||||
chr7:87547850 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1725+1488_1725+149 others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547850 | |||||||
chr7:87547885 | G | A | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+1463C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87547885 | |||||||
chr7:87548035 | T | A | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+1313A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548035 | |||||||
chr7:87548040 | T | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1725+1308A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548040 | |||||||
chr7:87548101 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1725+1247C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548101 | |||||||
chr7:87548117 | G | GAGGGGAG others(13): Show |
12 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(9): Show |
13 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725+1211_1725+123 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548117 | |||||||
chr7:87548137 | A | AAGGGG | 11 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(8): Show |
11 | HG01123.hp1 HG01981.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1725+1210_1725+121 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | |||||||
chr7:87548137 | A | AAGGGGAG others(18): Show |
1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1725+1210_1725+121 others(29): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | |||||||
chr7:87548137 | A | AAGGGGAG others(13): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0256 a0001c0001t0001g0257 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1725+1210_1725+121 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | |||||||
chr7:87548137 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1725+1211T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548137 | |||||||
chr7:87548142 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(157): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1725+1206T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548142 | |||||||
chr7:87548147 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(157): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1725+1201C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548147 | |||||||
chr7:87548147 | GAGGGAAG others(28): Show |
G | 1 | a0002c0002t0001g0246 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1725+1166_1725+120 others(39): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548147 | |||||||
chr7:87548152 | A | AAGGGG | 3 | a0001c0001t0002g0240 a0001c0004t0002g0045 a0001c0005t0001g0314 |
3 | HG01123.hp1 HG01981.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1725+1195_1725+119 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548152 | |||||||
chr7:87548152 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(157): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1725+1196T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548152 | |||||||
chr7:87548162 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(110): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1725+1186C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548162 | |||||||
chr7:87548162 | GAGGGAAA others(13): Show |
G | 127 | a0001c0001t0001g0051 a0001c0001t0001g0256 a0001c0001t0001g0257 others(124): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1725+1166_1725+118 others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548162 | |||||||
chr7:87548164 | GGGAAA | G | 30 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(27): Show |
30 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1725+1179_1725+118 others(9): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548164 | |||||||
chr7:87548167 | A | AAGGGAAG others(3): Show |
53 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1725+1180_1725+118 others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548167 | |||||||
chr7:87548167 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(110): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1725+1181T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548167 | |||||||
chr7:87548169 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1725+1179T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548169 | |||||||
chr7:87548182 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0056 others(193): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1725+1166T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548182 | |||||||
chr7:87548187 | A | G | 1 | a0001c0004t0012g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1725+1161T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548187 | |||||||
chr7:87548197 | A | G | 51 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1725+1151T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548197 | |||||||
chr7:87548260 | G | A | 1 | a0002c0002t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1725+1088C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548260 | |||||||
chr7:87548349 | A | G | 1 | a0001c0005t0003g0003 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1725+999T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548349 | |||||||
chr7:87548675 | G | A | 1 | a0001c0003t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1725+673C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548675 | |||||||
chr7:87548739 | C | T | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+609G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548739 | |||||||
chr7:87548740 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1725+608C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548740 | |||||||
chr7:87548827 | G | C | 1 | a0001c0004t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1725+521C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548827 | |||||||
chr7:87548899 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1725+449G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548899 | |||||||
chr7:87548900 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1725+448C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548900 | |||||||
chr7:87548927 | A | C | 1 | a0001c0003t0002g0141 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1725+421T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548927 | |||||||
chr7:87548963 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1725+385A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87548963 | |||||||
chr7:87549212 | C | A | 5 | a0001c0001t0019g0311 a0002c0010t0001g0090 a0003c0007t0008g0333 others(2): Show |
5 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+136G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87549212 | |||||||
chr7:87549310 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1725+38G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 14/27 | chr7 | 87549310 | |||||||
chr7:87549571 | A | C | 2 | a0002c0002t0002g0121 a0011c0029t0002g0130 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1555-53T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549571 | |||||||
chr7:87549761 | C | T | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1554+90G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549761 | |||||||
chr7:87549770 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1554+81C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549770 | |||||||
chr7:87549827 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1554+24T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 13/27 | chr7 | 87549827 | |||||||
chr7:87550127 | G | A | 21 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(18): Show |
21 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1350+44C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550127 | |||||||
chr7:87550130 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1350+41A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550130 | |||||||
chr7:87550154 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0004g0049 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1350+17G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 12/27 | chr7 | 87550154 | |||||||
chr7:87550300 | C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1225-4G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550300 | |||||||
chr7:87550358 | A | T | 1 | a0001c0003t0002g0252 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1225-62T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550358 | |||||||
chr7:87550379 | T | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1225-83A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 11/27 | chr7 | 87550379 | |||||||
chr7:87550619 | A | C | 3 | a0001c0003t0001g0109 a0001c0003t0001g0223 a0001c0003t0002g0228 |
3 | HG01934.hp1 HG02071.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1114-41T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 10/27 | chr7 | 87550619 | |||||||
chr7:87550882 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1000-44G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87550882 | |||||||
chr7:87550976 | A | G | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1000-138T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87550976 | |||||||
chr7:87551000 | A | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000-162T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551000 | |||||||
chr7:87551189 | T | A | 4 | a0002c0002t0001g0321 a0002c0002t0001g0322 a0002c0002t0001g0324 others(1): Show |
4 | NA19001.hp2 NA19074.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-351A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551189 | |||||||
chr7:87551244 | T | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1000-406A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551244 | |||||||
chr7:87551313 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1000-475T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551313 | |||||||
chr7:87551356 | G | A | 1 | a0003c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000-518C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551356 | |||||||
chr7:87551362 | A | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(218): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1000-524T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551362 | |||||||
chr7:87551422 | T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000-584A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551422 | |||||||
chr7:87551499 | A | T | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-661T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551499 | |||||||
chr7:87551650 | C | T | 3 | a0002c0002t0001g0142 a0002c0002t0001g0246 a0002c0002t0002g0139 |
3 | HG03704.hp2 NA18946.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1000-812G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551650 | |||||||
chr7:87551659 | T | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1000-821A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551659 | |||||||
chr7:87551659 | TA | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1000-822delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551659 | |||||||
chr7:87551716 | T | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000-878A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551716 | |||||||
chr7:87551859 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1000-1021G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551859 | |||||||
chr7:87551895 | G | A | 1 | a0001c0001t0002g0303 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1000-1057C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87551895 | |||||||
chr7:87552102 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1000-1264G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552102 | |||||||
chr7:87552329 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0005t0005g0021 |
3 | NA18998.hp1 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.999+1432A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552329 | |||||||
chr7:87552332 | A | G | 1 | a0001c0003t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.999+1429T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552332 | |||||||
chr7:87552382 | C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.999+1379G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552382 | |||||||
chr7:87552492 | C | T | 4 | a0001c0003t0006g0062 a0001c0003t0006g0081 a0001c0003t0009g0113 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+1269G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552492 | |||||||
chr7:87552533 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.999+1228C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552533 | |||||||
chr7:87552629 | C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.999+1132G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552629 | |||||||
chr7:87552647 | T | TA | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(8): Show |
12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+1113dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552647 | |||||||
chr7:87552653 | A | T | 5 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+1108T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552653 | |||||||
chr7:87552711 | G | GA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(133): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.999+1049dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552711 | |||||||
chr7:87552711 | G | GAA | 79 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(76): Show |
80 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.999+1048_999+1049d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552711 | |||||||
chr7:87552721 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.999+1040C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552721 | |||||||
chr7:87552941 | G | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999+820C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552941 | |||||||
chr7:87552976 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.999+785G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87552976 | |||||||
chr7:87553056 | A | G | 2 | a0001c0006t0001g0104 a0001c0006t0004g0103 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.999+705T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553056 | |||||||
chr7:87553108 | AT | A | 9 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(6): Show |
10 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+652delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553108 | |||||||
chr7:87553151 | G | A | 2 | a0001c0003t0001g0222 a0001c0003t0001g0230 |
2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.999+610C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553151 | |||||||
chr7:87553202 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.999+559C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553202 | |||||||
chr7:87553211 | C | T | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.999+550G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553211 | |||||||
chr7:87553212 | G | A | 2 | a0009c0030t0001g0242 a0009c0031t0002g0241 |
2 | NA18612.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.999+549C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553212 | |||||||
chr7:87553247 | A | C | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(8): Show |
12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+514T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553247 | |||||||
chr7:87553317 | C | CT | 51 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(48): Show |
52 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.999+443dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | |||||||
chr7:87553317 | C | CTT | 8 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0032 others(5): Show |
8 | HG02055.hp1 HG02886.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+442_999+443dup others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | |||||||
chr7:87553317 | CT | C | 9 | a0001c0001t0001g0084 a0001c0001t0004g0049 a0001c0001t0005g0034 others(6): Show |
9 | HG01243.hp2 HG01517.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+443delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553317 | |||||||
chr7:87553339 | T | TTTTGAGA others(3): Show |
1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.999+421_999+422ins others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553339 | |||||||
chr7:87553381 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.999+380G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553381 | |||||||
chr7:87553407 | G | A | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.999+354C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553407 | |||||||
chr7:87553413 | C | T | 1 | a0001c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.999+348G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553413 | |||||||
chr7:87553463 | G | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(189): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.999+298C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553463 | |||||||
chr7:87553482 | G | A | 1 | a0001c0003t0001g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.999+279C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553482 | |||||||
chr7:87553524 | G | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+237C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553524 | |||||||
chr7:87553555 | C | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.999+206G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553555 | |||||||
chr7:87553566 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.999+195A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553566 | |||||||
chr7:87553571 | C | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.999+190G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553571 | |||||||
chr7:87553599 | T | G | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(8): Show |
12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.999+162A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553599 | |||||||
chr7:87553626 | T | C | 1 | a0002c0002t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.999+135A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 9/27 | chr7 | 87553626 | |||||||
chr7:87554038 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.828-106A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554038 | |||||||
chr7:87554085 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.828-153A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554085 | |||||||
chr7:87554090 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.828-158G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554090 | |||||||
chr7:87554152 | T | C | 4 | a0002c0002t0001g0321 a0002c0002t0001g0322 a0002c0002t0001g0324 others(1): Show |
4 | NA19001.hp2 NA19074.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.828-220A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554152 | |||||||
chr7:87554304 | T | C | 2 | a0001c0004t0002g0107 a0001c0004t0020g0057 |
2 | HG02155.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.828-372A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554304 | |||||||
chr7:87554336 | T | TA | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(237): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.828-405dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554336 | |||||||
chr7:87554336 | T | TAA | 8 | a0001c0001t0001g0084 a0001c0001t0001g0282 a0001c0001t0004g0049 others(5): Show |
8 | HG00140.hp2 HG01243.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.828-406_828-405dup others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554336 | |||||||
chr7:87554467 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.828-535A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554467 | |||||||
chr7:87554526 | A | T | 1 | a0001c0003t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.828-594T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554526 | |||||||
chr7:87554547 | A | G | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0002 others(8): Show |
12 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.828-615T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554547 | |||||||
chr7:87554682 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.828-750G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554682 | |||||||
chr7:87554685 | C | T | 2 | a0001c0001t0019g0311 a0002c0010t0001g0090 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.828-753G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554685 | |||||||
chr7:87554866 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.828-934G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554866 | |||||||
chr7:87554921 | C | A | 1 | a0006c0011t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.828-989G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87554921 | |||||||
chr7:87555055 | C | T | 1 | a0002c0002t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.828-1123G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555055 | |||||||
chr7:87555107 | C | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.828-1175G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555107 | |||||||
chr7:87555263 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.828-1331C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555263 | |||||||
chr7:87555333 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.828-1401G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555333 | |||||||
chr7:87555408 | T | G | 2 | a0001c0004t0002g0053 a0001c0004t0002g0067 |
2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.828-1476A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555408 | |||||||
chr7:87555559 | A | G | 1 | a0001c0001t0006g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.828-1627T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555559 | |||||||
chr7:87555602 | A | G | 19 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(16): Show |
19 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.828-1670T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87555602 | |||||||
chr7:87556257 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.828-2325A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556257 | |||||||
chr7:87556382 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.828-2450A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556382 | |||||||
chr7:87556578 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(117): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.828-2646C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556578 | |||||||
chr7:87556663 | G | A | 27 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.828-2731C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556663 | |||||||
chr7:87556702 | C | G | 51 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.828-2770G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556702 | |||||||
chr7:87556836 | T | C | 28 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.828-2904A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556836 | |||||||
chr7:87556977 | A | G | 1 | a0002c0002t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828-3045T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87556977 | |||||||
chr7:87557350 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.828-3418G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557350 | |||||||
chr7:87557432 | A | G | 2 | a0002c0009t0001g0128 a0010c0028t0001g0146 |
2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.828-3500T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557432 | |||||||
chr7:87557873 | T | A | 3 | a0005c0012t0001g0271 a0005c0012t0001g0273 a0005c0017t0002g0272 |
3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.827+3390A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87557873 | |||||||
chr7:87558180 | C | T | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG00408.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+3083G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558180 | |||||||
chr7:87558225 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.827+3038A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558225 | |||||||
chr7:87558406 | G | A | 3 | a0006c0011t0001g0092 a0006c0011t0001g0093 a0006c0011t0001g0094 |
3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.827+2857C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558406 | |||||||
chr7:87558443 | T | C | 1 | a0001c0004t0012g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.827+2820A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558443 | |||||||
chr7:87558449 | C | T | 1 | a0004c0008t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.827+2814G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558449 | |||||||
chr7:87558467 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.827+2796T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558467 | |||||||
chr7:87558497 | A | C | 28 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+2766T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558497 | |||||||
chr7:87558651 | A | G | 1 | a0001c0005t0001g0293 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.827+2612T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558651 | |||||||
chr7:87558679 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.827+2584A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558679 | |||||||
chr7:87558682 | T | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.827+2581A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558682 | |||||||
chr7:87558731 | G | A | 9 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(6): Show |
10 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.827+2532C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558731 | |||||||
chr7:87558776 | C | T | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.827+2487G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87558776 | |||||||
chr7:87559093 | T | G | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.827+2170A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559093 | |||||||
chr7:87559151 | T | G | 52 | a0001c0001t0001g0084 a0001c0001t0001g0123 a0001c0001t0001g0125 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.827+2112A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559151 | |||||||
chr7:87559195 | A | G | 1 | a0001c0001t0011g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.827+2068T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559195 | |||||||
chr7:87559241 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0031 |
2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.827+2022C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559241 | |||||||
chr7:87559282 | G | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG00738.hp1 HG01261.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.827+1981C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559282 | |||||||
chr7:87559294 | C | T | 28 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+1969G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559294 | |||||||
chr7:87559408 | C | T | 6 | a0001c0001t0019g0311 a0001c0018t0017g0039 a0002c0010t0001g0090 others(3): Show |
6 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+1855G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559408 | |||||||
chr7:87559423 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0208 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.827+1840G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559423 | |||||||
chr7:87559542 | A | T | 2 | a0002c0002t0001g0142 a0002c0002t0002g0139 |
2 | HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.827+1721T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559542 | |||||||
chr7:87559588 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.827+1675A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559588 | |||||||
chr7:87559622 | T | C | 1 | a0001c0001t0007g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.827+1641A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559622 | |||||||
chr7:87559733 | C | G | 28 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.827+1530G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559733 | |||||||
chr7:87559868 | C | T | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.827+1395G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87559868 | |||||||
chr7:87560157 | T | C | 2 | a0001c0001t0001g0207 a0001c0005t0003g0003 |
3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.827+1106A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560157 | |||||||
chr7:87560170 | C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.827+1093G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560170 | |||||||
chr7:87560371 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827+892G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560371 | |||||||
chr7:87560401 | T | C | 1 | a0001c0004t0002g0064 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.827+862A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560401 | |||||||
chr7:87560464 | T | C | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.827+799A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560464 | |||||||
chr7:87560489 | A | G | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+774T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560489 | |||||||
chr7:87560522 | T | C | 2 | a0001c0004t0002g0107 a0001c0004t0020g0057 |
2 | HG02155.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.827+741A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560522 | |||||||
chr7:87560552 | T | C | 3 | a0002c0002t0001g0165 a0002c0002t0001g0178 a0002c0002t0001g0210 |
3 | HG00558.hp1 NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.827+711A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560552 | |||||||
chr7:87560614 | T | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(263): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.827+649A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560614 | |||||||
chr7:87560770 | A | G | 49 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.827+493T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87560770 | |||||||
chr7:87561136 | C | T | 27 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.827+127G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 8/27 | chr7 | 87561136 | |||||||
chr7:87561637 | A | G | 45 | a0001c0003t0001g0109 a0001c0003t0001g0161 a0001c0003t0001g0164 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.703-250T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561637 | |||||||
chr7:87561782 | T | G | 2 | a0001c0005t0001g0131 a0001c0005t0001g0276 |
2 | HG01169.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.703-395A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561782 | |||||||
chr7:87561838 | T | C | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-451A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561838 | |||||||
chr7:87561928 | G | A | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-541C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561928 | |||||||
chr7:87561930 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(188): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.703-543C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561930 | |||||||
chr7:87561963 | G | A | 5 | a0001c0003t0006g0081 a0001c0003t0009g0113 a0001c0006t0003g0023 others(2): Show |
6 | HG02622.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-576C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87561963 | |||||||
chr7:87562298 | C | T | 1 | a0001c0003t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.703-911G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562298 | |||||||
chr7:87562343 | A | G | 1 | a0001c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.703-956T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562343 | |||||||
chr7:87562353 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(124): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.703-966G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562353 | |||||||
chr7:87562406 | T | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703-1019A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562406 | |||||||
chr7:87562463 | A | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703-1076T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562463 | |||||||
chr7:87562532 | A | G | 27 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.703-1145T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562532 | |||||||
chr7:87562570 | TA | T | 4 | a0001c0001t0019g0311 a0002c0010t0001g0090 a0003c0007t0008g0333 others(1): Show |
4 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1184delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562570 | |||||||
chr7:87562630 | A | G | 5 | a0001c0001t0019g0311 a0001c0018t0017g0039 a0002c0010t0001g0090 others(2): Show |
5 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-1243T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562630 | |||||||
chr7:87562763 | G | GA | 28 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.703-1377dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562763 | |||||||
chr7:87562763 | GA | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0001g0101 others(19): Show |
22 | HG01243.hp2 HG01255.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.703-1377delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562763 | |||||||
chr7:87562930 | C | G | 27 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.703-1543G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562930 | |||||||
chr7:87562941 | A | G | 49 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0179 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.703-1554T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562941 | |||||||
chr7:87562959 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(119): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.703-1572G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562959 | |||||||
chr7:87562999 | G | T | 4 | a0001c0001t0019g0311 a0002c0010t0001g0090 a0003c0007t0008g0333 others(1): Show |
4 | HG01261.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1612C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87562999 | |||||||
chr7:87563205 | T | G | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-1818A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563205 | |||||||
chr7:87563415 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(217): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.703-2028C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563415 | |||||||
chr7:87563420 | A | G | 2 | a0004c0008t0001g0215 a0004c0008t0001g0217 |
2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.703-2033T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563420 | |||||||
chr7:87563665 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.703-2278G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563665 | |||||||
chr7:87563885 | C | T | 26 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(23): Show |
26 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.702+2185G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563885 | |||||||
chr7:87563984 | AG | A | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+2085delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87563984 | |||||||
chr7:87564144 | C | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.702+1926G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564144 | |||||||
chr7:87564281 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(56): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.702+1789C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564281 | |||||||
chr7:87564286 | A | G | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.702+1784T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564286 | |||||||
chr7:87564346 | C | T | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.702+1724G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564346 | |||||||
chr7:87564484 | A | G | 5 | a0001c0001t0005g0034 a0001c0018t0017g0039 a0002c0010t0001g0090 others(2): Show |
5 | HG01261.hp1 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+1586T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564484 | |||||||
chr7:87564720 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+1350C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564720 | |||||||
chr7:87564789 | G | A | 3 | a0002c0010t0001g0090 a0003c0007t0008g0333 a0003c0007t0008g0334 |
3 | HG01261.hp1 HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.702+1281C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564789 | |||||||
chr7:87564913 | T | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.702+1157A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564913 | |||||||
chr7:87564923 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+1147T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87564923 | |||||||
chr7:87565014 | T | G | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.702+1056A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565014 | |||||||
chr7:87565078 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+992G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565078 | |||||||
chr7:87565494 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.702+576C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565494 | |||||||
chr7:87565567 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+503C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565567 | |||||||
chr7:87565640 | T | TA | 22 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+429dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565640 | |||||||
chr7:87565657 | T | G | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+413A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565657 | |||||||
chr7:87565730 | G | T | 1 | a0002c0002t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.702+340C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565730 | |||||||
chr7:87565759 | T | G | 2 | a0001c0001t0004g0100 a0001c0001t0008g0098 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.702+311A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565759 | |||||||
chr7:87565790 | C | T | 150 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0084 others(147): Show |
153 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.702+280G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87565790 | |||||||
chr7:87566016 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+54C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87566016 | |||||||
chr7:87566026 | G | A | 1 | a0003c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.702+44C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 7/27 | chr7 | 87566026 | |||||||
chr7:87566433 | C | T | 1 | a0001c0005t0001g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531-192G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566433 | |||||||
chr7:87566534 | T | C | 124 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(121): Show |
127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.530+251A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566534 | |||||||
chr7:87566572 | T | C | 13 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0111 others(10): Show |
13 | HG00323.hp2 HG01081.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+213A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566572 | |||||||
chr7:87566580 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.530+205A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566580 | |||||||
chr7:87566646 | G | A | 124 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(121): Show |
127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.530+139C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 6/27 | chr7 | 87566646 | |||||||
chr7:87567297 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-321A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567297 | |||||||
chr7:87567743 | C | T | 124 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(121): Show |
127 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.339-767G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567743 | |||||||
chr7:87567789 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-813A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567789 | |||||||
chr7:87567821 | G | A | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.339-845C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567821 | |||||||
chr7:87567875 | A | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.339-899T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567875 | |||||||
chr7:87567899 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339-923G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567899 | |||||||
chr7:87567904 | C | T | 1 | a0001c0004t0002g0174 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.339-928G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567904 | |||||||
chr7:87567913 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.339-937A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567913 | |||||||
chr7:87567968 | G | A | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.339-992C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87567968 | |||||||
chr7:87568035 | A | G | 196 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0084 others(193): Show |
199 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.339-1059T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568035 | |||||||
chr7:87568221 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.339-1245G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568221 | |||||||
chr7:87568240 | G | GACAATAA others(14): Show |
1 | a0002c0002t0001g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.339-1285_339-1265d others(23): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568240 | |||||||
chr7:87568242 | C | CAAT | 59 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(56): Show |
61 | HG00423.hp2 HG01123.hp2 HG01175.hp1 others(58): Show |
intron_variant | MODIFIER | c.339-1269_339-1267d others(5): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | |||||||
chr7:87568242 | C | CAATAAT | 3 | a0001c0001t0006g0061 a0001c0018t0017g0039 a0002c0010t0002g0070 |
3 | HG02258.hp1 HG02723.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.339-1272_339-1267d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | |||||||
chr7:87568242 | C | CAATAATA others(17): Show |
114 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(111): Show |
117 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.339-1267_339-1266i others(26): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | |||||||
chr7:87568242 | C | CAATAATA others(20): Show |
6 | a0001c0003t0001g0222 a0001c0006t0001g0104 a0001c0006t0004g0103 others(3): Show |
6 | HG01358.hp1 HG01952.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-1267_339-1266i others(29): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568242 | |||||||
chr7:87568266 | T | TAATAATA others(4): Show |
51 | a0001c0001t0001g0065 a0001c0001t0001g0111 a0001c0001t0001g0112 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(13): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568266 | T | TAATAATA others(7): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0308 a0001c0001t0002g0083 others(1): Show |
4 | HG01106.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568266 | T | TAATAATA others(10): Show |
5 | a0001c0001t0001g0060 a0001c0001t0001g0260 a0001c0001t0001g0288 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568266 | T | TAATAATA others(13): Show |
5 | a0001c0001t0001g0087 a0001c0001t0003g0037 a0001c0001t0004g0085 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-1291_339-1290i others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568266 | T | TAATAATA others(16): Show |
2 | a0001c0001t0004g0086 a0001c0001t0008g0097 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.339-1291_339-1290i others(25): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568266 | T | TAATAATA others(19): Show |
1 | a0003c0007t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.339-1291_339-1290i others(28): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568266 | |||||||
chr7:87568267 | A | AATAATAA others(7): Show |
1 | a0001c0001t0004g0329 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.339-1292_339-1291i others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568267 | |||||||
chr7:87568278 | G | A | 121 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(118): Show |
124 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.339-1302C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568278 | |||||||
chr7:87568413 | C | CA | 72 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(69): Show |
72 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.339-1438dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568413 | |||||||
chr7:87568433 | A | C | 1 | a0001c0003t0001g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.339-1457T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568433 | |||||||
chr7:87568457 | T | A | 2 | a0001c0001t0001g0008 a0001c0001t0004g0007 |
4 | HG01175.hp1 HG01255.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-1481A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568457 | |||||||
chr7:87568695 | A | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0005t0001g0126 |
3 | HG00621.hp1 NA18959.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.338+1477T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568695 | |||||||
chr7:87568913 | T | C | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338+1259A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87568913 | |||||||
chr7:87569030 | T | G | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.338+1142A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569030 | |||||||
chr7:87569051 | G | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(40): Show |
43 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.338+1121C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569051 | |||||||
chr7:87569063 | C | T | 1 | a0002c0002t0002g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.338+1109G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569063 | |||||||
chr7:87569143 | G | A | 122 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(119): Show |
125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.338+1029C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569143 | |||||||
chr7:87569293 | A | G | 1 | a0001c0003t0001g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.338+879T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569293 | |||||||
chr7:87569332 | CA | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(76): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.338+839delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | |||||||
chr7:87569332 | CAA | C | 78 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(75): Show |
79 | HG00280.hp1 HG00639.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.338+838_338+839del others(2): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | |||||||
chr7:87569332 | CAAA | C | 177 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0084 others(174): Show |
180 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.338+837_338+839del others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569332 | |||||||
chr7:87569580 | T | TA | 10 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(7): Show |
11 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+591dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569580 | |||||||
chr7:87569728 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338+444G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569728 | |||||||
chr7:87569866 | G | A | 73 | a0001c0001t0002g0137 a0001c0003t0001g0156 a0001c0003t0001g0157 others(70): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.338+306C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569866 | |||||||
chr7:87569948 | C | A | 120 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(117): Show |
123 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338+224G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569948 | |||||||
chr7:87569949 | T | A | 120 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(117): Show |
123 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338+223A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569949 | |||||||
chr7:87569986 | A | C | 2 | a0001c0006t0001g0104 a0001c0006t0004g0103 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.338+186T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569986 | |||||||
chr7:87569987 | C | A | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.338+185G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87569987 | |||||||
chr7:87570049 | T | C | 32 | a0001c0003t0001g0109 a0001c0003t0001g0161 a0001c0003t0001g0164 others(29): Show |
32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.338+123A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87570049 | |||||||
chr7:87570096 | A | C | 13 | a0001c0001t0004g0049 a0001c0004t0002g0048 a0001c0004t0002g0052 others(10): Show |
13 | HG00423.hp2 HG03209.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+76T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 5/27 | chr7 | 87570096 | |||||||
chr7:87570248 | C | A | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-25G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570248 | |||||||
chr7:87570299 | A | G | 6 | a0001c0003t0002g0243 a0001c0003t0002g0244 a0001c0003t0002g0245 others(3): Show |
6 | HG00544.hp2 HG00609.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-76T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570299 | |||||||
chr7:87570362 | T | C | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287-139A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570362 | |||||||
chr7:87570648 | A | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-425T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570648 | |||||||
chr7:87570899 | A | G | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.287-676T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87570899 | |||||||
chr7:87571016 | G | T | 2 | a0001c0001t0001g0207 a0001c0005t0003g0003 |
3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.287-793C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571016 | |||||||
chr7:87571060 | T | C | 1 | a0002c0009t0013g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.287-837A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571060 | |||||||
chr7:87571151 | T | A | 271 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(268): Show |
275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-928A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571151 | |||||||
chr7:87571176 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-953T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571176 | |||||||
chr7:87571213 | G | A | 123 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0003g0037 others(120): Show |
126 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.287-990C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571213 | |||||||
chr7:87571322 | A | G | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0306 others(4): Show |
7 | HG01243.hp1 HG02486.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-1099T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571322 | |||||||
chr7:87571323 | T | C | 122 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(119): Show |
125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-1100A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571323 | |||||||
chr7:87571418 | G | C | 2 | a0001c0001t0001g0207 a0001c0005t0003g0003 |
3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.287-1195C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571418 | |||||||
chr7:87571457 | C | G | 271 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(268): Show |
275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-1234G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571457 | |||||||
chr7:87571499 | T | C | 2 | a0001c0006t0001g0104 a0001c0006t0004g0103 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.287-1276A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571499 | |||||||
chr7:87571526 | C | T | 271 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(268): Show |
275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.287-1303G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571526 | |||||||
chr7:87571620 | A | G | 6 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(3): Show |
6 | HG00438.hp1 HG02135.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-1397T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571620 | |||||||
chr7:87571645 | G | A | 1 | a0001c0001t0006g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-1422C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571645 | |||||||
chr7:87571675 | C | G | 1 | a0017c0032t0001g0110 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.287-1452G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571675 | |||||||
chr7:87571742 | A | G | 13 | a0001c0001t0004g0049 a0001c0004t0002g0048 a0001c0004t0002g0052 others(10): Show |
13 | HG00423.hp2 HG03209.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-1519T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571742 | |||||||
chr7:87571753 | C | T | 4 | a0001c0001t0003g0002 a0001c0001t0003g0027 a0001c0001t0010g0026 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-1530G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571753 | |||||||
chr7:87571769 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287-1546G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571769 | |||||||
chr7:87571770 | C | T | 122 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0004g0100 others(119): Show |
125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-1547G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571770 | |||||||
chr7:87571871 | C | G | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287-1648G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87571871 | |||||||
chr7:87572064 | T | C | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1841A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572064 | |||||||
chr7:87572166 | G | C | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1943C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572166 | |||||||
chr7:87572178 | T | TAG | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1956_287-1955i others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572178 | |||||||
chr7:87572179 | T | A | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1956A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572179 | |||||||
chr7:87572180 | T | G | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-1957A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572180 | |||||||
chr7:87572410 | G | A | 69 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0087 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-2187C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572410 | |||||||
chr7:87572436 | T | C | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2213A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572436 | |||||||
chr7:87572554 | T | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG00738.hp1 HG01261.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-2331A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572554 | |||||||
chr7:87572582 | A | G | 43 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(40): Show |
43 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.287-2359T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572582 | |||||||
chr7:87572771 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.287-2548T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87572771 | |||||||
chr7:87573086 | G | A | 190 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0084 others(187): Show |
193 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.287-2863C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573086 | |||||||
chr7:87573228 | T | C | 62 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0111 others(59): Show |
62 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.287-3005A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573228 | |||||||
chr7:87573236 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.287-3013C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573236 | |||||||
chr7:87573299 | C | T | 260 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(257): Show |
262 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.287-3076G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573299 | |||||||
chr7:87573308 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-3085C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573308 | |||||||
chr7:87573345 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.287-3122C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573345 | |||||||
chr7:87573484 | T | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.287-3261A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573484 | |||||||
chr7:87573758 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.287-3535T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573758 | |||||||
chr7:87573890 | C | CAA | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3668_287-3667i others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573890 | |||||||
chr7:87573891 | G | T | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3668C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87573891 | |||||||
chr7:87574188 | A | G | 2 | a0001c0003t0006g0081 a0001c0003t0009g0113 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.287-3965T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574188 | |||||||
chr7:87574289 | T | C | 3 | a0001c0001t0001g0195 a0003c0007t0008g0333 a0003c0007t0008g0334 |
3 | HG02109.hp1 HG02886.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.287-4066A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574289 | |||||||
chr7:87574500 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.287-4277T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574500 | |||||||
chr7:87574524 | C | T | 276 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(273): Show |
283 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(280): Show |
intron_variant | MODIFIER | c.287-4301G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574524 | |||||||
chr7:87574773 | C | T | 1 | a0001c0006t0004g0009 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.287-4550G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574773 | |||||||
chr7:87574867 | G | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.287-4644C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574867 | |||||||
chr7:87574963 | C | T | 255 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(252): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.287-4740G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87574963 | |||||||
chr7:87575221 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0002g0082 |
3 | HG02040.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.287-4998T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575221 | |||||||
chr7:87575294 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.287-5071G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575294 | |||||||
chr7:87575340 | G | A | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.287-5117C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575340 | |||||||
chr7:87575513 | T | C | 1 | a0001c0005t0001g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.287-5290A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575513 | |||||||
chr7:87575556 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-5333T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575556 | |||||||
chr7:87575589 | C | T | 22 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0036 others(19): Show |
22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.287-5366G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575589 | |||||||
chr7:87575743 | T | C | 1 | a0007c0014t0001g0340 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.287-5520A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575743 | |||||||
chr7:87575879 | C | T | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5656G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575879 | |||||||
chr7:87575881 | A | T | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5658T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87575881 | |||||||
chr7:87576158 | C | CT | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-5936dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576158 | |||||||
chr7:87576163 | T | A | 255 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(252): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.287-5940A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576163 | |||||||
chr7:87576347 | A | G | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.287-6124T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576347 | |||||||
chr7:87576361 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.287-6138A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576361 | |||||||
chr7:87576391 | T | C | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.287-6168A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576391 | |||||||
chr7:87576410 | AGT | A | 3 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 |
3 | HG01069.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.287-6189_287-6188d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576410 | |||||||
chr7:87576502 | A | G | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-6279T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576502 | |||||||
chr7:87576947 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.287-6724C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576947 | |||||||
chr7:87576972 | G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287-6749C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87576972 | |||||||
chr7:87577123 | A | G | 1 | a0002c0002t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-6900T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577123 | |||||||
chr7:87577299 | C | T | 2 | a0007c0014t0001g0339 a0007c0014t0001g0340 |
2 | HG01255.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.287-7076G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577299 | |||||||
chr7:87577573 | T | A | 2 | a0001c0004t0002g0044 a0001c0004t0002g0046 |
2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.287-7350A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577573 | |||||||
chr7:87577592 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0124 others(41): Show |
46 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-7369A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577592 | |||||||
chr7:87577639 | C | T | 3 | a0005c0012t0001g0271 a0005c0012t0001g0273 a0005c0017t0002g0272 |
3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.287-7416G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577639 | |||||||
chr7:87577812 | G | A | 183 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(180): Show |
187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.287-7589C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577812 | |||||||
chr7:87577821 | C | A | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287-7598G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577821 | |||||||
chr7:87577892 | T | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.286+7620A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577892 | |||||||
chr7:87577930 | C | A | 1 | a0001c0001t0004g0329 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.286+7582G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87577930 | |||||||
chr7:87578051 | A | C | 1 | a0002c0002t0001g0136 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.286+7461T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578051 | |||||||
chr7:87578132 | G | T | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.286+7380C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578132 | |||||||
chr7:87578222 | T | A | 1 | a0001c0003t0009g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+7290A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578222 | |||||||
chr7:87578297 | C | T | 16 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(13): Show |
16 | HG00738.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+7215G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578297 | |||||||
chr7:87578455 | G | A | 22 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0036 others(19): Show |
22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+7057C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578455 | |||||||
chr7:87578598 | C | T | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6914G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578598 | |||||||
chr7:87578659 | T | C | 1 | a0001c0006t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.286+6853A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578659 | |||||||
chr7:87578692 | CT | C | 257 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(254): Show |
264 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.286+6819delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578692 | |||||||
chr7:87578724 | C | T | 1 | a0002c0002t0002g0175 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.286+6788G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578724 | |||||||
chr7:87578909 | A | G | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6603T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578909 | |||||||
chr7:87578939 | T | C | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+6573A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87578939 | |||||||
chr7:87579061 | TA | T | 5 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+6450delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579061 | |||||||
chr7:87579065 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0124 others(41): Show |
46 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.286+6447A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579065 | |||||||
chr7:87579172 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6340C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579172 | |||||||
chr7:87579239 | C | T | 1 | a0001c0004t0002g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.286+6273G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579239 | |||||||
chr7:87579363 | T | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6149A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579363 | |||||||
chr7:87579390 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6122C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579390 | |||||||
chr7:87579488 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0330 |
2 | HG00408.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.286+6024A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579488 | |||||||
chr7:87579671 | G | A | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+5841C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579671 | |||||||
chr7:87579759 | G | A | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286+5753C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579759 | |||||||
chr7:87579766 | T | A | 22 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0036 others(19): Show |
22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+5746A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579766 | |||||||
chr7:87579790 | G | C | 1 | a0001c0001t0002g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.286+5722C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579790 | |||||||
chr7:87579834 | G | A | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+5678C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87579834 | |||||||
chr7:87580056 | T | C | 255 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(252): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.286+5456A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580056 | |||||||
chr7:87580067 | T | C | 1 | a0002c0002t0011g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.286+5445A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580067 | |||||||
chr7:87580103 | A | C | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+5409T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580103 | |||||||
chr7:87580276 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.286+5236C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580276 | |||||||
chr7:87580299 | G | T | 1 | a0001c0004t0002g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.286+5213C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580299 | |||||||
chr7:87580440 | A | G | 2 | a0002c0002t0001g0006 a0002c0002t0001g0166 |
3 | NA18970.hp1 NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.286+5072T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580440 | |||||||
chr7:87580609 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.286+4903T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580609 | |||||||
chr7:87580674 | G | A | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+4838C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580674 | |||||||
chr7:87580685 | C | T | 2 | a0001c0004t0005g0011 a0001c0004t0005g0012 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.286+4827G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580685 | |||||||
chr7:87580820 | A | G | 1 | a0002c0009t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.286+4692T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580820 | |||||||
chr7:87580863 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.286+4649C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580863 | |||||||
chr7:87580943 | A | G | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+4569T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87580943 | |||||||
chr7:87581271 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0004g0100 others(1): Show |
4 | HG02280.hp2 HG03579.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+4241A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581271 | |||||||
chr7:87581381 | G | C | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+4131C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581381 | |||||||
chr7:87581541 | C | T | 4 | a0001c0005t0001g0209 a0001c0005t0001g0284 a0001c0005t0001g0285 others(1): Show |
4 | NA18948.hp2 NA18979.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3971G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581541 | |||||||
chr7:87581658 | C | A | 255 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(252): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.286+3854G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581658 | |||||||
chr7:87581729 | T | A | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+3783A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581729 | |||||||
chr7:87581750 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0250 a0001c0001t0004g0329 others(1): Show |
4 | HG00323.hp2 HG01081.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+3762A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581750 | |||||||
chr7:87581844 | C | T | 4 | a0001c0001t0003g0002 a0001c0001t0003g0027 a0001c0001t0010g0026 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+3668G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581844 | |||||||
chr7:87581866 | G | C | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.286+3646C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87581866 | |||||||
chr7:87582004 | G | A | 1 | a0001c0001t0006g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.286+3508C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582004 | |||||||
chr7:87582091 | G | A | 1 | a0001c0005t0002g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+3421C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582091 | |||||||
chr7:87582170 | G | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0111 others(61): Show |
67 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+3342C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582170 | |||||||
chr7:87582171 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0031 |
2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.286+3341C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582171 | |||||||
chr7:87582277 | T | C | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+3235A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582277 | |||||||
chr7:87582512 | C | T | 4 | a0001c0005t0001g0131 a0002c0002t0001g0331 a0002c0002t0002g0121 others(1): Show |
4 | HG01496.hp1 HG02280.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+3000G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582512 | |||||||
chr7:87582598 | T | C | 6 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0004g0182 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+2914A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582598 | |||||||
chr7:87582612 | G | C | 1 | a0002c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.286+2900C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582612 | |||||||
chr7:87582619 | T | C | 1 | a0001c0001t0008g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.286+2893A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582619 | |||||||
chr7:87582672 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.286+2840C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582672 | |||||||
chr7:87582948 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0004g0100 |
3 | HG02280.hp2 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.286+2564T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87582948 | |||||||
chr7:87583068 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.286+2444C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583068 | |||||||
chr7:87583088 | G | A | 3 | a0005c0012t0001g0271 a0005c0012t0001g0273 a0005c0017t0002g0272 |
3 | HG00741.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.286+2424C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583088 | |||||||
chr7:87583145 | G | A | 22 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0036 others(19): Show |
22 | HG00423.hp2 HG02109.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.286+2367C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583145 | |||||||
chr7:87583273 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+2239T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583273 | |||||||
chr7:87583674 | T | A | 71 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0108 others(68): Show |
74 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.286+1838A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583674 | |||||||
chr7:87583710 | AGTTTACT others(8): Show |
A | 15 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0002g0048 others(12): Show |
15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1787_286+1801d others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583710 | |||||||
chr7:87583728 | G | T | 15 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0002g0048 others(12): Show |
15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1784C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583728 | |||||||
chr7:87583729 | T | C | 15 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0002g0048 others(12): Show |
15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1783A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583729 | |||||||
chr7:87583813 | G | C | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+1699C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583813 | |||||||
chr7:87583916 | A | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0111 others(61): Show |
67 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+1596T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583916 | |||||||
chr7:87583937 | C | T | 1 | a0001c0005t0005g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.286+1575G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583937 | |||||||
chr7:87583942 | C | T | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+1570G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87583942 | |||||||
chr7:87584048 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0250 |
2 | HG01081.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.286+1464C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584048 | |||||||
chr7:87584068 | C | T | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.286+1444G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584068 | |||||||
chr7:87584562 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.286+950C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584562 | |||||||
chr7:87584585 | C | T | 128 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(125): Show |
132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.286+927G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584585 | |||||||
chr7:87584936 | A | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0005t0001g0314 |
3 | HG01123.hp1 HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.286+576T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584936 | |||||||
chr7:87584951 | A | AC | 52 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(49): Show |
52 | HG01192.hp1 HG01358.hp2 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.286+560dupG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584951 | |||||||
chr7:87584959 | A | C | 127 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(124): Show |
128 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.286+553T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584959 | |||||||
chr7:87584961 | A | C | 13 | a0001c0001t0001g0108 a0001c0001t0001g0191 a0001c0001t0001g0192 others(10): Show |
13 | HG01978.hp2 HG02027.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.286+551T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87584961 | |||||||
chr7:87585076 | C | T | 47 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0063 others(44): Show |
47 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.286+436G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585076 | |||||||
chr7:87585192 | T | C | 15 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0002g0048 others(12): Show |
15 | HG00423.hp2 NA18948.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+320A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585192 | |||||||
chr7:87585215 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+297G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585215 | |||||||
chr7:87585373 | T | C | 10 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0003t0006g0081 others(7): Show |
11 | HG01261.hp1 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+139A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 4/27 | chr7 | 87585373 | |||||||
chr7:87585786 | C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.118-106G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585786 | |||||||
chr7:87585798 | A | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0051 others(333): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.118-118T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585798 | |||||||
chr7:87585988 | G | A | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.118-308C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87585988 | |||||||
chr7:87586279 | G | A | 4 | a0001c0001t0002g0240 a0001c0001t0002g0301 a0001c0001t0002g0302 others(1): Show |
4 | HG00423.hp1 NA18949.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-599C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586279 | |||||||
chr7:87586372 | A | T | 1 | a0002c0024t0001g0184 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118-692T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586372 | |||||||
chr7:87586425 | C | G | 1 | a0006c0011t0001g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.118-745G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586425 | |||||||
chr7:87586449 | G | A | 3 | a0001c0003t0006g0081 a0001c0003t0009g0113 a0001c0006t0003g0023 |
3 | HG02622.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.118-769C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586449 | |||||||
chr7:87586834 | G | A | 277 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(274): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.118-1154C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586834 | |||||||
chr7:87586900 | AAG | A | 253 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0056 others(250): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.118-1222_118-1221d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87586900 | |||||||
chr7:87587106 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.118-1426G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587106 | |||||||
chr7:87587108 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-1428C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587108 | |||||||
chr7:87587249 | T | C | 1 | a0001c0001t0019g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118-1569A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587249 | |||||||
chr7:87587279 | C | T | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.118-1599G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587279 | |||||||
chr7:87587351 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-1671G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587351 | |||||||
chr7:87587375 | A | G | 4 | a0001c0004t0005g0013 a0001c0004t0005g0014 a0001c0004t0005g0016 others(1): Show |
4 | NA18988.hp2 NA18990.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1695T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587375 | |||||||
chr7:87587431 | A | C | 2 | a0001c0006t0001g0104 a0001c0006t0004g0103 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.118-1751T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587431 | |||||||
chr7:87587471 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0208 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.118-1791G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587471 | |||||||
chr7:87587488 | T | C | 1 | a0001c0003t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.118-1808A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587488 | |||||||
chr7:87587501 | G | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0111 others(58): Show |
64 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.118-1821C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587501 | |||||||
chr7:87587507 | A | G | 1 | a0002c0002t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.118-1827T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587507 | |||||||
chr7:87587597 | T | C | 1 | a0001c0003t0001g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.118-1917A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587597 | |||||||
chr7:87587600 | A | G | 3 | a0001c0003t0001g0231 a0013c0026t0014g0010 a0014c0019t0009g0237 |
3 | HG00438.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.118-1920T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587600 | |||||||
chr7:87587610 | A | G | 4 | a0001c0003t0001g0231 a0002c0002t0001g0129 a0013c0026t0014g0010 others(1): Show |
4 | HG00438.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1930T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587610 | |||||||
chr7:87587647 | A | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0309 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-1967T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587647 | |||||||
chr7:87587744 | A | G | 10 | a0001c0001t0001g0188 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
11 | HG00140.hp2 HG00621.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-2064T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587744 | |||||||
chr7:87587755 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-2075T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587755 | |||||||
chr7:87587770 | G | A | 2 | a0001c0001t0004g0100 a0001c0018t0017g0039 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.118-2090C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587770 | |||||||
chr7:87587832 | A | G | 1 | a0002c0002t0001g0319 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-2152T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587832 | |||||||
chr7:87587845 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2165T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587845 | |||||||
chr7:87587849 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2169A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587849 | |||||||
chr7:87587854 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-2174C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587854 | |||||||
chr7:87587857 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2177T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587857 | |||||||
chr7:87587861 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-2181A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587861 | |||||||
chr7:87587861 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118-2181A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587861 | |||||||
chr7:87587874 | C | CA | 45 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(42): Show |
45 | HG01123.hp2 HG01192.hp1 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.118-2195dupT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | |||||||
chr7:87587874 | C | CAA | 8 | a0001c0001t0006g0059 a0001c0001t0008g0097 a0001c0004t0002g0050 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-2196_118-2195d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | |||||||
chr7:87587874 | CA | C | 153 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0101 others(150): Show |
157 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-2195delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587874 | |||||||
chr7:87587899 | T | C | 137 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(134): Show |
141 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.118-2219A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587899 | |||||||
chr7:87587929 | A | T | 1 | a0002c0002t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.118-2249T>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587929 | |||||||
chr7:87587947 | CT | C | 132 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(129): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.118-2268delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87587947 | |||||||
chr7:87588156 | G | GT | 16 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0010g0035 others(13): Show |
16 | HG00423.hp2 HG02572.hp1 NA18952.hp2 others(13): Show |
intron_variant | MODIFIER | c.118-2477dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588156 | |||||||
chr7:87588156 | GT | G | 106 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0116 others(103): Show |
110 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.118-2477delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588156 | |||||||
chr7:87588255 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.118-2575A>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588255 | |||||||
chr7:87588340 | C | T | 1 | a0015c0027t0001g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.118-2660G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588340 | |||||||
chr7:87588348 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-2668C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588348 | |||||||
chr7:87588431 | G | T | 2 | a0001c0004t0002g0053 a0001c0004t0002g0067 |
2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.118-2751C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588431 | |||||||
chr7:87588514 | G | A | 2 | a0006c0011t0001g0093 a0006c0011t0001g0094 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.118-2834C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588514 | |||||||
chr7:87588646 | A | G | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.118-2966T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588646 | |||||||
chr7:87588704 | G | A | 1 | a0001c0006t0003g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-3024C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588704 | |||||||
chr7:87588807 | A | G | 1 | a0004c0008t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118-3127T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588807 | |||||||
chr7:87588886 | C | T | 14 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0002g0048 others(11): Show |
14 | HG00423.hp2 NA18952.hp2 NA18963.hp2 others(11): Show |
intron_variant | MODIFIER | c.118-3206G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87588886 | |||||||
chr7:87589031 | A | G | 181 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(178): Show |
185 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.118-3351T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589031 | |||||||
chr7:87589059 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.118-3379G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589059 | |||||||
chr7:87589161 | T | A | 1 | a0001c0004t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.118-3481A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589161 | |||||||
chr7:87589191 | G | A | 1 | a0001c0004t0002g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.118-3511C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589191 | |||||||
chr7:87589315 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.118-3635A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589315 | |||||||
chr7:87589423 | C | T | 1 | a0002c0002t0002g0121 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.118-3743G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589423 | |||||||
chr7:87589491 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.118-3811T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589491 | |||||||
chr7:87589701 | C | A | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0009g0267 others(2): Show |
5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-4021G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589701 | |||||||
chr7:87589761 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG01515.hp1 HG01517.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.118-4081C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589761 | |||||||
chr7:87589805 | G | GAGAGAGA others(12): Show |
1 | a0001c0001t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-4126_118-4125i others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGA | 28 | a0001c0001t0001g0119 a0001c0001t0001g0180 a0001c0001t0001g0239 others(25): Show |
28 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.118-4127_118-4126d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGA | 21 | a0001c0001t0001g0250 a0001c0001t0001g0305 a0001c0001t0001g0306 others(18): Show |
21 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.118-4129_118-4126d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGA | 16 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0260 others(13): Show |
16 | HG00323.hp2 HG00639.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.118-4131_118-4126d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(1): Show |
12 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0313 others(9): Show |
13 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-4133_118-4126d others(10): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(3): Show |
6 | a0001c0001t0003g0018 a0001c0004t0002g0047 a0001c0004t0002g0069 others(3): Show |
6 | HG01123.hp2 HG02717.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-4135_118-4126d others(12): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(5): Show |
15 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0003g0020 others(12): Show |
15 | HG00423.hp2 HG01192.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.118-4137_118-4126d others(14): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(7): Show |
4 | a0001c0001t0001g0051 a0001c0001t0003g0036 a0001c0004t0002g0075 others(1): Show |
4 | HG02897.hp2 NA18952.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4139_118-4126d others(16): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(9): Show |
15 | a0001c0001t0001g0056 a0001c0001t0001g0181 a0001c0001t0006g0058 others(12): Show |
15 | HG01496.hp2 HG01952.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-4141_118-4126d others(18): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(11): Show |
13 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0073 others(10): Show |
13 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-4143_118-4126d others(20): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(13): Show |
1 | a0001c0001t0004g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-4145_118-4126d others(22): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(15): Show |
2 | a0001c0001t0005g0034 a0013c0026t0014g0010 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.118-4147_118-4126d others(24): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(19): Show |
2 | a0001c0001t0004g0089 a0001c0001t0004g0100 |
2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.118-4151_118-4126d others(28): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | G | GGAGAGAG others(23): Show |
1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.118-4155_118-4126d others(32): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | GGA | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0185 others(1): Show |
4 | HG03041.hp2 HG03225.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4127_118-4126d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589805 | GGAGA | G | 5 | a0001c0001t0001g0278 a0001c0001t0001g0317 a0001c0001t0004g0007 others(2): Show |
6 | HG00735.hp2 HG01175.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-4129_118-4126d others(6): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589805 | |||||||
chr7:87589836 | G | GA | 9 | a0001c0001t0001g0269 a0001c0004t0002g0174 a0001c0004t0002g0270 others(6): Show |
9 | HG01358.hp1 HG03831.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-4157_118-4156i others(3): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589836 | G | GAGAGAGA others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-4157_118-4156i others(13): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589836 | G | GAGAGAGA others(6): Show |
1 | a0001c0001t0003g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-4157_118-4156i others(15): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589836 | G | GAGAGAGA others(8): Show |
5 | a0001c0001t0001g0065 a0001c0001t0001g0087 a0001c0001t0006g0066 others(2): Show |
5 | HG01081.hp1 HG01358.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4157_118-4156i others(17): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589836 | G | GAGAGAGA others(10): Show |
2 | a0001c0001t0001g0068 a0001c0004t0002g0067 |
2 | NA18906.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.118-4157_118-4156i others(19): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589836 | G | GAGAGAGA others(12): Show |
1 | a0001c0001t0004g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.118-4157_118-4156i others(21): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589836 | |||||||
chr7:87589837 | G | A | 1 | a0001c0001t0004g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118-4157C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589837 | |||||||
chr7:87589849 | G | GGA | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0004t0001g0071 others(4): Show |
7 | HG01123.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4171_118-4170d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589849 | |||||||
chr7:87589849 | G | GGAGAGA | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(1): Show |
4 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-4175_118-4170d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589849 | |||||||
chr7:87589853 | A | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
6 | HG00408.hp2 HG00597.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-4173T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589853 | |||||||
chr7:87589860 | G | A | 2 | a0001c0001t0010g0035 a0003c0007t0003g0033 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-4180C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87589860 | |||||||
chr7:87590165 | G | C | 108 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(105): Show |
112 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.118-4485C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590165 | |||||||
chr7:87590519 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-4839T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590519 | |||||||
chr7:87590633 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118-4953G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87590633 | |||||||
chr7:87591018 | T | C | 89 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(86): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.117+4748A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591018 | |||||||
chr7:87591246 | C | T | 105 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(102): Show |
109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.117+4520G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591246 | |||||||
chr7:87591255 | A | G | 1 | a0001c0001t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+4511T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591255 | |||||||
chr7:87591390 | C | T | 1 | a0003c0007t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117+4376G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591390 | |||||||
chr7:87591398 | A | C | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+4368T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591398 | |||||||
chr7:87591466 | C | T | 2 | a0001c0001t0010g0035 a0003c0007t0003g0033 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.117+4300G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591466 | |||||||
chr7:87591499 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.117+4267C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591499 | |||||||
chr7:87591570 | A | G | 178 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(175): Show |
182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.117+4196T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591570 | |||||||
chr7:87591575 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0278 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+4191G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591575 | |||||||
chr7:87591770 | G | T | 1 | a0013c0026t0014g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.117+3996C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591770 | |||||||
chr7:87591900 | A | G | 105 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(102): Show |
109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.117+3866T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591900 | |||||||
chr7:87591902 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.117+3864C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87591902 | |||||||
chr7:87592306 | T | C | 1 | a0003c0007t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117+3460A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592306 | |||||||
chr7:87592362 | C | T | 9 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0036 others(6): Show |
9 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+3404G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592362 | |||||||
chr7:87592482 | C | A | 23 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0018 others(20): Show |
23 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.117+3284G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592482 | |||||||
chr7:87592859 | CCTAAGA | C | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+2901_117+2906d others(8): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592859 | |||||||
chr7:87592928 | C | CT | 7 | a0001c0001t0001g0073 a0001c0001t0001g0108 a0001c0003t0001g0109 others(4): Show |
7 | HG02572.hp2 HG02717.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+2837dupA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | |||||||
chr7:87592928 | C | CTT | 35 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(32): Show |
35 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.117+2836_117+2837d others(4): Show |
ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | |||||||
chr7:87592928 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0087 others(83): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.117+2837delA | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592928 | |||||||
chr7:87592962 | C | G | 24 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0018 others(21): Show |
24 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+2804G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87592962 | |||||||
chr7:87593161 | T | A | 35 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0002 others(32): Show |
37 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.117+2605A>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593161 | |||||||
chr7:87593232 | T | C | 1 | a0001c0003t0001g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.117+2534A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593232 | |||||||
chr7:87593365 | TA | T | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+2400delT | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593365 | |||||||
chr7:87593440 | T | C | 2 | a0001c0006t0001g0104 a0001c0006t0004g0103 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.117+2326A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593440 | |||||||
chr7:87593557 | T | C | 8 | a0002c0002t0001g0319 a0002c0002t0001g0320 a0002c0002t0001g0321 others(5): Show |
8 | HG01975.hp1 NA18941.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+2209A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87593557 | |||||||
chr7:87594212 | C | A | 2 | a0001c0006t0004g0009 a0001c0006t0004g0327 |
3 | HG02965.hp2 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+1554G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594212 | |||||||
chr7:87594312 | G | C | 12 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0005g0011 others(9): Show |
12 | HG00423.hp2 NA18952.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+1454C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594312 | |||||||
chr7:87594383 | A | G | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1383T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594383 | |||||||
chr7:87594423 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+1343G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594423 | |||||||
chr7:87594647 | C | T | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1119G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594647 | |||||||
chr7:87594715 | G | T | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+1051C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594715 | |||||||
chr7:87594864 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.117+902G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594864 | |||||||
chr7:87594935 | C | T | 46 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(43): Show |
46 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.117+831G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87594935 | |||||||
chr7:87595112 | C | T | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+654G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595112 | |||||||
chr7:87595113 | A | G | 36 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0002 others(33): Show |
38 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.117+653T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595113 | |||||||
chr7:87595264 | T | C | 2 | a0001c0001t0004g0329 a0001c0005t0001g0328 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.117+502A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595264 | |||||||
chr7:87595348 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.117+418G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595348 | |||||||
chr7:87595367 | G | A | 9 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0036 others(6): Show |
9 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+399C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595367 | |||||||
chr7:87595385 | C | T | 1 | a0001c0005t0016g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+381G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595385 | |||||||
chr7:87595456 | C | A | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+310G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595456 | |||||||
chr7:87595632 | C | G | 11 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+134G>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595632 | |||||||
chr7:87595730 | G | A | 35 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0003g0002 others(32): Show |
37 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.117+36C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 3/27 | chr7 | 87595730 | |||||||
chr7:87595857 | A | G | 1 | a0001c0005t0007g0076 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69-43T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595857 | |||||||
chr7:87595965 | C | A | 1 | a0001c0001t0010g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-151G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595965 | |||||||
chr7:87595996 | A | G | 1 | a0002c0002t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.69-182T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87595996 | |||||||
chr7:87596610 | TG | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0004g0085 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-797delC | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596610 | |||||||
chr7:87596847 | G | C | 1 | a0001c0004t0002g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.69-1033C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596847 | |||||||
chr7:87596992 | A | C | 3 | a0006c0011t0001g0092 a0006c0011t0001g0093 a0006c0011t0001g0094 |
3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.69-1178T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87596992 | |||||||
chr7:87597348 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69-1534T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87597348 | |||||||
chr7:87597374 | A | G | 1 | a0002c0010t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-1560T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87597374 | |||||||
chr7:87598040 | C | A | 1 | a0001c0001t0002g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.68+2077G>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598040 | |||||||
chr7:87598217 | T | C | 1 | a0002c0002t0001g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68+1900A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598217 | |||||||
chr7:87598327 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0004g0085 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+1790G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598327 | |||||||
chr7:87598428 | A | G | 7 | a0001c0004t0001g0043 a0001c0004t0002g0041 a0001c0004t0002g0044 others(4): Show |
7 | HG01358.hp2 HG01496.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1689T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598428 | |||||||
chr7:87598544 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.68+1573T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598544 | |||||||
chr7:87598589 | A | C | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68+1528T>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598589 | |||||||
chr7:87598605 | T | C | 1 | a0002c0002t0001g0332 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.68+1512A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598605 | |||||||
chr7:87598744 | T | C | 2 | a0003c0007t0008g0333 a0003c0007t0008g0334 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.68+1373A>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598744 | |||||||
chr7:87598951 | G | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.68+1166C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87598951 | |||||||
chr7:87599243 | G | C | 2 | a0001c0001t0002g0337 a0001c0001t0002g0338 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+874C>G | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599243 | |||||||
chr7:87599700 | G | A | 3 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.68+417C>T | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599700 | |||||||
chr7:87599709 | C | T | 12 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0027 others(9): Show |
14 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.68+408G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599709 | |||||||
chr7:87599743 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.68+374T>C | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599743 | |||||||
chr7:87599944 | C | T | 1 | a0001c0003t0006g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+173G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 2/27 | chr7 | 87599944 | |||||||
chr7:87600263 | TC | T | 36 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(33): Show |
36 | HG01081.hp1 HG01123.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-74delG | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600263 | |||||||
chr7:87600518 | C | T | 1 | a0001c0018t0017g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+237G>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600518 | |||||||
chr7:87600615 | G | T | 13 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0004t0005g0011 others(10): Show |
13 | HG00423.hp2 HG03098.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+140C>A | ABCB1 | ENSG00000085563.15 | transcript | ENST00000622132.5 | protein_coding | 1/27 | chr7 | 87600615 |