Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10060 |
|---|---|
| ensemblid | ENSG00000069431.14 |
| hgncid | 60 |
| symbol | ABCC9 |
| name | ATP binding cassette subfamily C member 9 |
| refseq_nuc | NM_020297.4 |
| refseq_prot | NP_064693.2 |
| ensembl_nuc | ENST00000261200.9 |
| ensembl_prot | ENSP00000261200.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 21797389 |
| end | 21941426 |
| strand | - |
| ver | v1.2 |
| region | chr12:21797389-21941426 |
| region5000 | chr12:21792389-21946426 |
| regionname0 | ABCC9_chr12_21797389_21941426 |
| regionname5000 | ABCC9_chr12_21792389_21946426 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1549 | 208 | 77 | 33 | 68 | 10 | 18 | 46 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0002 | 0/0 | 1549 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0003 | 0/0 | 1549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0004 | 0/0 | 1549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4650 | 187 | 64 | 33 | 60 | 10 | 18 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0002 | 0/0 | 4650 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0003 | 0/0 | 4650 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0004 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0005 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0006 | 0/0 | 4650 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0007 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0008 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0009 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0010 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0011 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| c0012 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4019 | 167 | 52 | 27 | 63 | 7 | 16 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0002 | 0/0 | 4017 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0003 | 0/0 | 4019 | 5 | 0 | 3 | 0 | 2 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0004 | 0/0 | 4018 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0005 | 0/0 | 4015 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0006 | 0/0 | 4013 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0007 | 0/0 | 4019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0008 | 0/0 | 4019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0009 | 0/0 | 4019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0010 | 0/0 | 4019 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0011 | 0/0 | 4019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0012 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0013 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0014 | 0/0 | 4018 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0015 | 0/0 | 4019 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0016 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0017 | 0/0 | 4019 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0018 | 0/0 | 4019 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0019 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0020 | 0/0 | 4019 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0021 | 0/0 | 4019 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0022 | 0/0 | 4019 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0023 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| t0024 | 0/0 | 4019 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4650 | 187 | 64 | 33 | 60 | 10 | 18 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0002 | 0/0 | 4650 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0003 | 0/0 | 4650 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0004 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0005 | 0/0 | 4650 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0006 | 0/0 | 4650 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0008 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0009 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0010 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0002c0007 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0003c0012 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0004c0011 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8668 | 150 | 44 | 26 | 55 | 7 | 16 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0002 | 0/0 | 8666 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0003 | 0/0 | 8668 | 5 | 0 | 3 | 0 | 2 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0004 | 0/0 | 8667 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0005 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0006 | 0/0 | 8662 | 3 | 0 | 3 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0008 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0009 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0010 | 0/0 | 8668 | 2 | 0 | 0 | 2 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0011 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0013 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0014 | 0/0 | 8667 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0015 | 0/0 | 8668 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0017 | 0/0 | 8668 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0018 | 0/0 | 8668 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0019 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0020 | 0/0 | 8668 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0021 | 0/0 | 8668 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0022 | 0/0 | 8668 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0001t0024 | 0/0 | 8668 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0002t0001 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0002t0004 | 0/0 | 8667 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0002t0012 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0002t0023 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0003t0007 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0003t0009 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0003t0016 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0004t0001 | 0/0 | 8668 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0005t0001 | 0/0 | 8668 | 3 | 0 | 0 | 3 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0006t0001 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0006t0005 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0008t0001 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0009t0001 | 0/0 | 8668 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0001c0010t0001 | 0/0 | 8668 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0002c0007t0001 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0003c0012t0001 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| a0004c0011t0001 | 0/0 | 8668 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | copy fasta | chr12 | 21792389 | 21946426 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0018g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0020g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0021g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0022g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0002t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0002t0023g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0003t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0003t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0003t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0003t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0005t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0006t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0006t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0008t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0001c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0002c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0002c0007t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0003c0012t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| a0004c0011t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0147 | EUR | GBR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00280 | hp1 | a0001 | c0001 | t0022 | g0018 | EUR | FIN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0062 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0143 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01261 | hp1 | a0004 | c0011 | t0001 | g0149 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01993 | hp1 | a0001 | c0001 | t0020 | g0140 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02074 | hp1 | a0001 | c0001 | t0024 | g0211 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02074 | hp2 | a0001 | c0001 | t0015 | g0170 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02572 | hp2 | a0001 | c0003 | t0016 | g0173 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0092 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02647 | hp2 | a0001 | c0006 | t0005 | g0192 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02698 | hp1 | a0001 | c0001 | t0021 | g0122 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0188 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0189 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0120 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02965 | hp1 | a0001 | c0002 | t0023 | g0182 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0183 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02976 | hp2 | a0001 | c0003 | t0007 | g0180 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03041 | hp1 | a0002 | c0007 | t0001 | g0039 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03098 | hp1 | a0001 | c0002 | t0012 | g0002 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03098 | hp2 | a0001 | c0003 | t0009 | g0209 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0204 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0042 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0191 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0196 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03669 | hp1 | a0001 | c0001 | t0018 | g0003 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18906 | hp1 | a0003 | c0012 | t0001 | g0195 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18962 | hp2 | a0001 | c0010 | t0001 | g0054 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18981 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19063 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19090 | hp1 | a0001 | c0009 | t0001 | g0101 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19091 | hp1 | a0001 | c0001 | t0010 | g0064 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0071 | AFR | YRI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0141 | EUR | TSI | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG02559 | hp2 | a0002 | c0007 | t0001 | g0049 | AFR | ACB | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | USA | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| NA21309 | hp2 | a0001 | c0008 | t0001 | g0179 | AFR | LWK | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | ABCC9_chr12_21792389_21946426 | ABCC9 | chr12 | 21792389 | 21946426 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21842378
|
C | T | 1 | a0002 | 2 | HG02559.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.3409G>A | p.Val1137Ile | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/40 | 3772/8668 | 3409/4650 | 1137/1549 | chr12 | 21842378 | ||
| chr12:21875660
|
G | A | 1 | a0004 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.2086C>T | p.Pro696Ser | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/40 | 2449/8668 | 2086/4650 | 696/1549 | chr12 | 21875660 | ||
| chr12:21912885
|
T | A | 1 | a0003 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.998A>T | p.Asn333Ile | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/40 | 1361/8668 | 998/4650 | 333/1549 | chr12 | 21912885 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21801158
|
C | T | 1 | a0001c0010 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.4536G>A | p.Thr1512Thr | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 4899/8668 | 4536/4650 | 1512/1549 | chr12 | 21801158 | ||
| chr12:21842430
|
C | T | 1 | a0001c0004 | 3 | NA18977.hp2 NA18992.hp2 NA19063.hp2 |
synonymous_variant | LOW | c.3357G>A | p.Leu1119Leu | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/40 | 3720/8668 | 3357/4650 | 1119/1549 | chr12 | 21842430 | ||
| chr12:21842466
|
G | A | 1 | a0001c0003 | 4 | HG02572.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.3321C>T | p.Ile1107Ile | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/40 | 3684/8668 | 3321/4650 | 1107/1549 | chr12 | 21842466 | ||
| chr12:21848154
|
G | A | 1 | a0001c0005 | 3 | NA18981.hp1 NA19063.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.2862C>T | p.Asp954Asp | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/40 | 3225/8668 | 2862/4650 | 954/1549 | chr12 | 21848154 | ||
| chr12:21852380
|
C | T | 1 | a0001c0009 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.2631G>A | p.Thr877Thr | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/40 | 2994/8668 | 2631/4650 | 877/1549 | chr12 | 21852380 | ||
| chr12:21887889
|
G | A | 2 | a0001c0002a0003c0012 | 6 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1848C>T | p.Asp616Asp | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/40 | 2211/8668 | 1848/4650 | 616/1549 | chr12 | 21887889 | ||
| chr12:21913031
|
A | T | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.852T>A | p.Ser284Ser | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/40 | 1215/8668 | 852/4650 | 284/1549 | chr12 | 21913031 | ||
| chr12:21915695
|
G | A | 1 | a0001c0006 | 3 | HG02647.hp2 HG03195.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.789C>T | p.Cys263Cys | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/40 | 1152/8668 | 789/4650 | 263/1549 | chr12 | 21915695 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21797499
|
G | A | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3545C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 3545 | chr12 | 21797499 | |||||
| chr12:21797555
|
TATAGGC | T | 1 | a0001c0001t0006 | 3 | HG00639.hp1 HG00738.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3483_*3488delGCCT others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 3483 | chr12 | 21797555 | |||||
| chr12:21797764
|
T | C | 5 | a0001c0001t0005a0001c0001t0009a0001c0003t0009others(2): Show | 6 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3280A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 3280 | chr12 | 21797764 | |||||
| chr12:21797781
|
T | C | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3263A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 3263 | chr12 | 21797781 | |||||
| chr12:21798119
|
T | G | 1 | a0001c0001t0019 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2925 | chr12 | 21798119 | |||||
| chr12:21798173
|
A | G | 1 | a0001c0001t0018 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2871T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2871 | chr12 | 21798173 | |||||
| chr12:21798243
|
C | T | 2 | a0001c0001t0005a0001c0006t0005 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2801G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2801 | chr12 | 21798243 | |||||
| chr12:21798504
|
G | A | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2540C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2540 | chr12 | 21798504 | |||||
| chr12:21798507
|
GTTGT | G | 2 | a0001c0001t0005a0001c0006t0005 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2533_*2536delACAA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2533 | chr12 | 21798507 | |||||
| chr12:21798583
|
G | T | 2 | a0001c0001t0005a0001c0006t0005 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2461C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2461 | chr12 | 21798583 | |||||
| chr12:21798604
|
G | T | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(2): Show | 13 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2440 | chr12 | 21798604 | |||||
| chr12:21798797
|
C | T | 1 | a0001c0001t0017 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2247G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2247 | chr12 | 21798797 | |||||
| chr12:21798851
|
T | A | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2193A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2193 | chr12 | 21798851 | |||||
| chr12:21798871
|
G | A | 1 | a0001c0001t0020 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2173 | chr12 | 21798871 | |||||
| chr12:21798897
|
C | G | 1 | a0001c0001t0003 | 5 | HG00140.hp2 HG01169.hp1 HG01934.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2147G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 2147 | chr12 | 21798897 | |||||
| chr12:21799066
|
G | A | 1 | a0001c0001t0021 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1978C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1978 | chr12 | 21799066 | |||||
| chr12:21799117
|
G | C | 1 | a0001c0003t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1927 | chr12 | 21799117 | |||||
| chr12:21799194
|
A | G | 3 | a0001c0001t0005a0001c0001t0011a0001c0006t0005 | 5 | HG02109.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1850T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1850 | chr12 | 21799194 | |||||
| chr12:21799247
|
TA | T | 3 | a0001c0001t0004a0001c0001t0014a0001c0002t0004 | 5 | HG02145.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1796delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1796 | chr12 | 21799247 | |||||
| chr12:21799247
|
TAA | T | 2 | a0001c0001t0002a0001c0002t0012 | 8 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1795_*1796delTT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1795 | chr12 | 21799247 | |||||
| chr12:21799260
|
A | T | 1 | a0001c0001t0010 | 2 | HG00408.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1784T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1784 | chr12 | 21799260 | |||||
| chr12:21799601
|
G | A | 1 | a0001c0003t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1443 | chr12 | 21799601 | |||||
| chr12:21799727
|
T | A | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1317A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1317 | chr12 | 21799727 | |||||
| chr12:21799826
|
C | T | 3 | a0001c0001t0009a0001c0003t0009a0001c0003t0016 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1218G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1218 | chr12 | 21799826 | |||||
| chr12:21800003
|
A | T | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(2): Show | 13 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1041T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 1041 | chr12 | 21800003 | |||||
| chr12:21800162
|
A | C | 1 | a0001c0001t0015 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 882 | chr12 | 21800162 | |||||
| chr12:21800193
|
C | G | 1 | a0001c0001t0008 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*851G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 851 | chr12 | 21800193 | |||||
| chr12:21800268
|
T | C | 1 | a0001c0001t0022 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 776 | chr12 | 21800268 | |||||
| chr12:21800373
|
C | A | 1 | a0001c0002t0023 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 671 | chr12 | 21800373 | |||||
| chr12:21800525
|
C | G | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(2): Show | 13 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 519 | chr12 | 21800525 | |||||
| chr12:21800568
|
A | G | 1 | a0001c0001t0014 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 476 | chr12 | 21800568 | |||||
| chr12:21800719
|
A | G | 1 | a0001c0001t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 325 | chr12 | 21800719 | |||||
| chr12:21801025
|
A | G | 1 | a0001c0003t0007 | 2 | HG02976.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 40/40 | 19 | chr12 | 21801025 | |||||
| chr12:21941251
|
A | T | 1 | a0001c0002t0012 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-188T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 1/40 | 4577 | chr12 | 21941251 | |||||
| chr12:21941322
|
G | A | 1 | a0001c0001t0024 | 1 | HG02074.hp1 | 5_prime_UTR_variant | MODIFIER | c.-259C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 1/40 | 4648 | chr12 | 21941322 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21801344
|
A | T | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4513-163T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801344 | ||||||
| chr12:21801421
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4513-240T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801421 | ||||||
| chr12:21801432
|
G | A | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4513-251C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801432 | ||||||
| chr12:21801484
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4513-303C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801484 | ||||||
| chr12:21801814
|
G | A | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4513-633C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801814 | ||||||
| chr12:21801893
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4513-712G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801893 | ||||||
| chr12:21801896
|
T | A | 2 | a0001c0001t0009g0129a0001c0003t0016g0173 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.4513-715A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21801896 | ||||||
| chr12:21802139
|
TC | T | 3 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0006t0005g0192 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4513-959delG | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802139 | ||||||
| chr12:21802358
|
C | G | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4513-1177G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802358 | ||||||
| chr12:21802395
|
T | C | 3 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0006t0005g0192 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4513-1214A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802395 | ||||||
| chr12:21802402
|
C | CACAAG | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 38 | HG00621.hp1 HG00639.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.4513-1226_4513-122 others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802402 | ||||||
| chr12:21802692
|
A | C | 2 | a0001c0001t0001g0044a0002c0007t0001g0039 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4513-1511T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802692 | ||||||
| chr12:21802860
|
G | T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4513-1679C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802860 | ||||||
| chr12:21802900
|
T | C | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4513-1719A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802900 | ||||||
| chr12:21802905
|
G | T | 3 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0006t0005g0192 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4513-1724C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802905 | ||||||
| chr12:21802972
|
T | C | 3 | a0001c0001t0009g0129a0001c0003t0009g0209a0001c0003t0016g0173 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4513-1791A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21802972 | ||||||
| chr12:21803066
|
C | T | 1 | a0001c0001t0018g0003 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4513-1885G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803066 | ||||||
| chr12:21803069
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4513-1888G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803069 | ||||||
| chr12:21803130
|
T | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4513-1949A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803130 | ||||||
| chr12:21803203
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4513-2022G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803203 | ||||||
| chr12:21803256
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4513-2075G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803256 | ||||||
| chr12:21803314
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4513-2133A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803314 | ||||||
| chr12:21803319
|
A | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4513-2138T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803319 | ||||||
| chr12:21803421
|
G | A | 3 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0006t0005g0192 | 3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4513-2240C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803421 | ||||||
| chr12:21803433
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4513-2252C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803433 | ||||||
| chr12:21803443
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4513-2262C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803443 | ||||||
| chr12:21803449
|
G | A | 3 | a0001c0001t0009g0129a0001c0003t0009g0209a0001c0003t0016g0173 | 3 | HG02572.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4513-2268C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803449 | ||||||
| chr12:21803450
|
G | C | 4 | a0001c0001t0024g0211a0001c0004t0001g0135a0001c0005t0001g0006others(1): Show | 4 | HG02074.hp1 NA18981.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.4513-2269C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803450 | ||||||
| chr12:21803591
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4512+2407C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803591 | ||||||
| chr12:21803656
|
C | CA | 11 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0117others(8): Show | 11 | HG00140.hp1 HG01891.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.4512+2341dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803656 | ||||||
| chr12:21803656
|
CA | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.4512+2341delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803656 | ||||||
| chr12:21803656
|
CAAA | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(33): Show | 37 | HG00621.hp1 HG01255.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.4512+2339_4512+234 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803656 | ||||||
| chr12:21803675
|
AC | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4512+2322delG | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803675 | ||||||
| chr12:21803782
|
A | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4512+2216T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803782 | ||||||
| chr12:21803858
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4512+2140C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803858 | ||||||
| chr12:21803921
|
G | T | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4512+2077C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21803921 | ||||||
| chr12:21804004
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0038 | 3 | HG02257.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4512+1994A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21804004 | ||||||
| chr12:21804258
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0133 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4512+1740C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21804258 | ||||||
| chr12:21804744
|
A | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0031others(4): Show | 7 | NA18747.hp1 NA18959.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.4512+1254T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21804744 | ||||||
| chr12:21804753
|
G | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4512+1245C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21804753 | ||||||
| chr12:21804904
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0193 | 2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4512+1094A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21804904 | ||||||
| chr12:21805396
|
T | C | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4512+602A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21805396 | ||||||
| chr12:21805465
|
G | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(68): Show | 71 | HG00621.hp1 HG00639.hp2 HG01261.hp2 others(68): Show |
intron_variant | MODIFIER | c.4512+533C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21805465 | ||||||
| chr12:21805668
|
T | G | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4512+330A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 39/39 | chr12 | 21805668 | ||||||
| chr12:21806064
|
CA | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.4450-5delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21806064 | ||||||
| chr12:21806420
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4450-360T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21806420 | ||||||
| chr12:21806454
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4450-394A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21806454 | ||||||
| chr12:21806560
|
A | G | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4450-500T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21806560 | ||||||
| chr12:21806968
|
T | C | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4449+378A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21806968 | ||||||
| chr12:21807035
|
G | A | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4449+311C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21807035 | ||||||
| chr12:21807142
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4449+204C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21807142 | ||||||
| chr12:21807200
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4449+146T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 38/39 | chr12 | 21807200 | ||||||
| chr12:21807695
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0153 | 2 | HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4316-216A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21807695 | ||||||
| chr12:21807946
|
AT | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4316-468delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21807946 | ||||||
| chr12:21808222
|
G | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4316-743C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808222 | ||||||
| chr12:21808422
|
A | C | 3 | a0001c0001t0005g0175a0001c0001t0011g0068a0001c0001t0011g0120 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4316-943T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808422 | ||||||
| chr12:21808575
|
G | C | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4316-1096C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808575 | ||||||
| chr12:21808765
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4315+1087G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808765 | ||||||
| chr12:21808778
|
C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG00621.hp2 HG01106.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.4315+1073dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808778 | ||||||
| chr12:21808778
|
CA | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(12): Show | 15 | HG01516.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.4315+1073delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808778 | ||||||
| chr12:21808778
|
CAAA | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4315+1071_4315+107 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808778 | ||||||
| chr12:21808792
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 38 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.4315+1060T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808792 | ||||||
| chr12:21808794
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4315+1058T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808794 | ||||||
| chr12:21808796
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4315+1056T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808796 | ||||||
| chr12:21808820
|
T | G | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4315+1032A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808820 | ||||||
| chr12:21808865
|
G | A | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4315+987C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808865 | ||||||
| chr12:21808916
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4315+936A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21808916 | ||||||
| chr12:21809163
|
CA | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4315+688delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21809163 | ||||||
| chr12:21809391
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4315+461T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21809391 | ||||||
| chr12:21809435
|
G | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4315+417C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21809435 | ||||||
| chr12:21809522
|
A | T | 3 | a0001c0001t0006g0027a0001c0001t0006g0142a0001c0001t0006g0210 | 3 | HG00639.hp1 HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.4315+330T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 37/39 | chr12 | 21809522 | ||||||
| chr12:21810084
|
C | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4212-129G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810084 | ||||||
| chr12:21810240
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4212-285T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810240 | ||||||
| chr12:21810332
|
T | C | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4212-377A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810332 | ||||||
| chr12:21810411
|
G | T | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4212-456C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810411 | ||||||
| chr12:21810439
|
T | C | 17 | a0001c0001t0001g0019a0001c0001t0002g0033a0001c0001t0002g0043others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.4212-484A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810439 | ||||||
| chr12:21810816
|
A | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4212-861T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810816 | ||||||
| chr12:21810962
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4212-1007T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21810962 | ||||||
| chr12:21811114
|
T | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4211+935A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811114 | ||||||
| chr12:21811166
|
G | A | 2 | a0001c0001t0001g0044a0002c0007t0001g0039 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4211+883C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811166 | ||||||
| chr12:21811215
|
G | A | 9 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0078others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.4211+834C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811215 | ||||||
| chr12:21811237
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4211+812G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811237 | ||||||
| chr12:21811284
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(67): Show |
intron_variant | MODIFIER | c.4211+765C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811284 | ||||||
| chr12:21811315
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4211+734A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811315 | ||||||
| chr12:21811508
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4211+541G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811508 | ||||||
| chr12:21811642
|
A | G | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4211+407T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811642 | ||||||
| chr12:21811727
|
G | A | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4211+322C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811727 | ||||||
| chr12:21811797
|
G | A | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4211+252C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811797 | ||||||
| chr12:21811926
|
T | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4211+123A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811926 | ||||||
| chr12:21811941
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4211+108G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 36/39 | chr12 | 21811941 | ||||||
| chr12:21812236
|
T | C | 14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4103-79A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812236 | ||||||
| chr12:21812239
|
CTTAG | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG01981.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4103-86_4103-83del others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812239 | ||||||
| chr12:21812321
|
C | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4103-164G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812321 | ||||||
| chr12:21812503
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.4103-346C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812503 | ||||||
| chr12:21812633
|
A | G | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4103-476T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812633 | ||||||
| chr12:21812667
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4103-510C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812667 | ||||||
| chr12:21812824
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4103-667A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21812824 | ||||||
| chr12:21813097
|
T | C | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4103-940A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813097 | ||||||
| chr12:21813428
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.4102+1216C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813428 | ||||||
| chr12:21813575
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4102+1069T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813575 | ||||||
| chr12:21813596
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4102+1048C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813596 | ||||||
| chr12:21813767
|
T | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(70): Show | 73 | HG00621.hp1 HG00639.hp2 HG01261.hp2 others(70): Show |
intron_variant | MODIFIER | c.4102+877A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813767 | ||||||
| chr12:21813842
|
A | C | 1 | a0001c0001t0004g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4102+802T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813842 | ||||||
| chr12:21813891
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4102+753G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21813891 | ||||||
| chr12:21814042
|
T | A | 5 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0001t0019g0196others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.4102+602A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814042 | ||||||
| chr12:21814123
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4102+521A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814123 | ||||||
| chr12:21814177
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4102+467C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814177 | ||||||
| chr12:21814221
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4102+423C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814221 | ||||||
| chr12:21814278
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4102+366A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814278 | ||||||
| chr12:21814467
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4102+177T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814467 | ||||||
| chr12:21814588
|
GT | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4102+55delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814588 | ||||||
| chr12:21814617
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4102+27T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 35/39 | chr12 | 21814617 | ||||||
| chr12:21814912
|
A | AT | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4024-191dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 34/39 | chr12 | 21814912 | ||||||
| chr12:21815097
|
G | A | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4024-375C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 34/39 | chr12 | 21815097 | ||||||
| chr12:21815286
|
G | GT | 11 | a0001c0001t0001g0044a0001c0001t0001g0107a0001c0001t0001g0109others(8): Show | 11 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4023+476dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 34/39 | chr12 | 21815286 | ||||||
| chr12:21815286
|
GT | G | 30 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(27): Show | 30 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4023+476delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 34/39 | chr12 | 21815286 | ||||||
| chr12:21815436
|
T | C | 3 | a0001c0003t0007g0180a0001c0003t0007g0204a0001c0003t0009g0209 | 3 | HG02976.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4023+327A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 34/39 | chr12 | 21815436 | ||||||
| chr12:21816026
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3893-133G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816026 | ||||||
| chr12:21816036
|
G | GT | 7 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0177others(4): Show | 7 | HG00408.hp1 HG01346.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3893-144dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTT | 11 | a0001c0001t0001g0024a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 11 | HG00621.hp2 HG01884.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.3893-145_3893-144d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTTT | 5 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0069others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3893-146_3893-144d others(5): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTTTT | 6 | a0001c0001t0001g0085a0001c0001t0001g0097a0001c0005t0001g0016others(3): Show | 6 | HG01496.hp2 HG01516.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3893-147_3893-144d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTTTTTTT | 5 | a0001c0001t0001g0050a0001c0001t0001g0103a0001c0001t0001g0166others(2): Show | 5 | HG00738.hp1 HG01433.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3893-150_3893-144d others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0086 | 2 | HG01168.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3893-153_3893-144d others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0133a0001c0006t0001g0042 | 2 | HG01169.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3893-154_3893-144d others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0111others(6): Show | 9 | HG00558.hp2 HG01074.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.3893-150_3893-144d others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(1): Show |
G | 17 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0047others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.3893-151_3893-144d others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(2): Show |
G | 21 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.3893-152_3893-144d others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(3): Show |
G | 13 | a0001c0001t0001g0026a0001c0001t0001g0058a0001c0001t0001g0099others(10): Show | 13 | HG00738.hp2 HG01175.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.3893-153_3893-144d others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(4): Show |
G | 9 | a0001c0001t0001g0061a0001c0001t0001g0082a0001c0001t0001g0093others(6): Show | 9 | HG01175.hp1 HG01255.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.3893-154_3893-144d others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3893-156_3893-144d others(15): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(7): Show |
G | 7 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0059others(4): Show | 7 | HG00621.hp1 HG00639.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.3893-157_3893-144d others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(8): Show |
G | 29 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 30 | HG01255.hp2 HG01346.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.3893-158_3893-144d others(17): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(9): Show |
G | 7 | a0001c0001t0001g0004a0001c0001t0001g0083a0001c0001t0001g0134others(4): Show | 7 | HG01106.hp2 HG01993.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3893-159_3893-144d others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(10): Show |
G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0034others(5): Show | 8 | HG02572.hp2 HG02723.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.3893-160_3893-144d others(19): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(11): Show |
G | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3893-161_3893-144d others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(13): Show |
G | 3 | a0001c0003t0007g0180a0001c0003t0007g0204a0001c0006t0005g0192 | 3 | HG02647.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3893-163_3893-144d others(22): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(16): Show |
G | 3 | a0001c0001t0004g0023a0001c0001t0005g0067a0001c0001t0005g0175 | 3 | HG02109.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3893-166_3893-144d others(25): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(18): Show |
G | 13 | a0001c0001t0001g0019a0001c0001t0002g0033a0001c0001t0002g0043others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3893-168_3893-144d others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(19): Show |
G | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3893-169_3893-144d others(28): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816036
|
GTTTTTTT others(21): Show |
G | 2 | a0001c0001t0019g0196a0001c0002t0023g0182 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3893-171_3893-144d others(30): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816036 | ||||||
| chr12:21816055
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3893-162A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816055 | ||||||
| chr12:21816056
|
T | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0059others(4): Show | 7 | HG00621.hp1 HG00639.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.3893-163A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816056 | ||||||
| chr12:21816057
|
T | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(25): Show | 29 | HG01255.hp2 HG01346.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.3893-164A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816057 | ||||||
| chr12:21816058
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3893-165A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816058 | ||||||
| chr12:21816063
|
T | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG01981.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3893-170A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816063 | ||||||
| chr12:21816080
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3893-187A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816080 | ||||||
| chr12:21816138
|
T | C | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3893-245A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816138 | ||||||
| chr12:21816188
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3893-295G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816188 | ||||||
| chr12:21816196
|
A | G | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3893-303T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816196 | ||||||
| chr12:21816502
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(65): Show | 69 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3893-609A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816502 | ||||||
| chr12:21816841
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0133 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3892+346G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816841 | ||||||
| chr12:21816842
|
G | A | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0006t0005g0192 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3892+345C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816842 | ||||||
| chr12:21816963
|
G | A | 8 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0001t0019g0196others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3892+224C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21816963 | ||||||
| chr12:21817085
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(67): Show |
intron_variant | MODIFIER | c.3892+102G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 33/39 | chr12 | 21817085 | ||||||
| chr12:21817372
|
G | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3772-65C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817372 | ||||||
| chr12:21817439
|
G | T | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3772-132C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817439 | ||||||
| chr12:21817510
|
A | G | 1 | a0001c0001t0006g0027 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3772-203T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817510 | ||||||
| chr12:21817546
|
C | G | 4 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0001t0011g0068others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-239G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817546 | ||||||
| chr12:21817557
|
A | G | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3772-250T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817557 | ||||||
| chr12:21817649
|
C | T | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3772-342G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817649 | ||||||
| chr12:21817814
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3771+336G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817814 | ||||||
| chr12:21817922
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3771+228G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21817922 | ||||||
| chr12:21818005
|
C | T | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3771+145G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21818005 | ||||||
| chr12:21818045
|
T | G | 1 | a0001c0010t0001g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3771+105A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 32/39 | chr12 | 21818045 | ||||||
| chr12:21818311
|
A | G | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3670-60T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818311 | ||||||
| chr12:21818345
|
C | A | 7 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3670-94G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818345 | ||||||
| chr12:21818458
|
A | ATATATC | 4 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0001t0011g0068others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3670-213_3670-208d others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818458 | ||||||
| chr12:21818458
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3670-207T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818458 | ||||||
| chr12:21818458
|
ATATATC | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(36): Show | 40 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.3670-213_3670-208d others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818458 | ||||||
| chr12:21818472
|
ATATCTAT others(3): Show |
A | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3670-231_3670-222d others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818472 | ||||||
| chr12:21818478
|
ATATC | A | 13 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0078others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3670-231_3670-228d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818478 | ||||||
| chr12:21818490
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3670-239T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818490 | ||||||
| chr12:21818492
|
A | C | 1 | a0001c0001t0015g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3670-241T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818492 | ||||||
| chr12:21818524
|
A | ATG | 5 | a0001c0001t0005g0175a0001c0001t0011g0068a0001c0001t0011g0120others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3670-274_3670-273i others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818524 | ||||||
| chr12:21818526
|
A | ATG | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(36): Show | 40 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.3670-277_3670-276d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
A | ATGTG | 4 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0057others(1): Show | 4 | HG02040.hp2 HG02293.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.3670-279_3670-276d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
A | ATGTGTG | 10 | a0001c0001t0002g0033a0001c0001t0002g0126a0001c0001t0002g0202others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3670-281_3670-276d others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0002g0078a0001c0001t0002g0128a0001c0002t0012g0002 | 3 | HG02723.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3670-283_3670-276d others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3670-287_3670-276d others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
A | G | 6 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0001t0011g0068others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3670-275T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
ATG | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0032others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.3670-277_3670-276d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
ATGTG | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0047others(15): Show | 18 | HG00558.hp2 HG00621.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3670-279_3670-276d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
ATGTGTG | A | 2 | a0001c0001t0001g0020a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3670-281_3670-276d others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818526
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0019g0196a0001c0002t0023g0182 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3670-285_3670-276d others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818526 | ||||||
| chr12:21818528
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3670-277C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818528 | ||||||
| chr12:21818532
|
G | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3670-281C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818532 | ||||||
| chr12:21818534
|
G | A | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3670-283C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818534 | ||||||
| chr12:21818536
|
G | A | 2 | a0001c0003t0009g0209a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3670-285C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818536 | ||||||
| chr12:21818538
|
G | A | 2 | a0001c0001t0019g0196a0001c0002t0023g0182 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3670-287C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818538 | ||||||
| chr12:21818644
|
CT | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0031others(33): Show | 36 | HG01169.hp1 HG01516.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.3670-394delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818644 | ||||||
| chr12:21818644
|
CTT | C | 7 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(4): Show | 7 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.3670-395_3670-394d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818644 | ||||||
| chr12:21818666
|
G | T | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3670-415C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818666 | ||||||
| chr12:21818679
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3670-428T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818679 | ||||||
| chr12:21818714
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3670-463C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818714 | ||||||
| chr12:21818755
|
A | G | 6 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3670-504T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818755 | ||||||
| chr12:21818778
|
T | C | 4 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0001t0011g0068others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3670-527A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21818778 | ||||||
| chr12:21819105
|
C | T | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3670-854G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819105 | ||||||
| chr12:21819190
|
A | T | 7 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3670-939T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819190 | ||||||
| chr12:21819221
|
A | C | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3670-970T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819221 | ||||||
| chr12:21819349
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3670-1098G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819349 | ||||||
| chr12:21819355
|
T | C | 1 | a0001c0002t0004g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3670-1104A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819355 | ||||||
| chr12:21819371
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.3670-1120A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819371 | ||||||
| chr12:21819630
|
A | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0031 | 2 | NA18959.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3670-1379T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819630 | ||||||
| chr12:21819688
|
C | CT | 6 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0113others(3): Show | 6 | HG00408.hp1 HG02129.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.3670-1438dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819688 | ||||||
| chr12:21819741
|
T | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02129.hp2 NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.3670-1490A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819741 | ||||||
| chr12:21819885
|
T | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3670-1634A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819885 | ||||||
| chr12:21819910
|
G | A | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3670-1659C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21819910 | ||||||
| chr12:21820022
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3670-1771A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820022 | ||||||
| chr12:21820077
|
A | G | 7 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3670-1826T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820077 | ||||||
| chr12:21820081
|
A | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0040others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.3670-1830T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820081 | ||||||
| chr12:21820141
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3670-1890C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820141 | ||||||
| chr12:21820142
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3670-1891C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820142 | ||||||
| chr12:21820504
|
C | CTA | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0151 | 3 | HG01074.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3670-2255_3670-225 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820504 | ||||||
| chr12:21820757
|
T | G | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3670-2506A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820757 | ||||||
| chr12:21820914
|
G | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3670-2663C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820914 | ||||||
| chr12:21820918
|
A | G | 7 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0003t0007g0180others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3670-2667T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820918 | ||||||
| chr12:21820990
|
T | C | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3670-2739A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21820990 | ||||||
| chr12:21821084
|
G | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0028others(8): Show | 11 | HG01993.hp2 HG02040.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.3670-2833C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821084 | ||||||
| chr12:21821130
|
ACTTTT | A | 2 | a0001c0001t0019g0196a0001c0002t0023g0182 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3670-2884_3670-288 others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821130 | ||||||
| chr12:21821236
|
A | C | 1 | a0001c0001t0024g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3670-2985T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821236 | ||||||
| chr12:21821254
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02809.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3670-3003G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821254 | ||||||
| chr12:21821294
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0040others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.3670-3043A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821294 | ||||||
| chr12:21821326
|
A | G | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3670-3075T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821326 | ||||||
| chr12:21821481
|
T | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3670-3230A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821481 | ||||||
| chr12:21821677
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3670-3426T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821677 | ||||||
| chr12:21821767
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3670-3516C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821767 | ||||||
| chr12:21821903
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3670-3652C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821903 | ||||||
| chr12:21821949
|
C | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3670-3698G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21821949 | ||||||
| chr12:21822064
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3670-3813A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822064 | ||||||
| chr12:21822069
|
T | C | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0008t0001g0179 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3670-3818A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822069 | ||||||
| chr12:21822172
|
T | C | 2 | a0001c0001t0019g0196a0001c0002t0023g0182 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3670-3921A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822172 | ||||||
| chr12:21822249
|
G | A | 14 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0078others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3670-3998C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822249 | ||||||
| chr12:21822330
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0159 | 2 | HG01175.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.3670-4079T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822330 | ||||||
| chr12:21822355
|
T | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3670-4104A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822355 | ||||||
| chr12:21822389
|
G | A | 1 | a0001c0001t0021g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3670-4138C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822389 | ||||||
| chr12:21822428
|
T | A | 10 | a0001c0001t0005g0067a0001c0001t0005g0175a0001c0001t0009g0129others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.3670-4177A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822428 | ||||||
| chr12:21822486
|
G | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 66 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(63): Show |
intron_variant | MODIFIER | c.3670-4235C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822486 | ||||||
| chr12:21822581
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3670-4330G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822581 | ||||||
| chr12:21822596
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3670-4345C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822596 | ||||||
| chr12:21822632
|
T | TACTAAAA others(2): Show |
65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 66 | HG00621.hp1 HG00639.hp2 HG01255.hp2 others(63): Show |
intron_variant | MODIFIER | c.3670-4382_3670-438 others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822632 | ||||||
| chr12:21822769
|
C | T | 1 | a0001c0001t0006g0027 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3670-4518G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822769 | ||||||
| chr12:21822790
|
C | CA | 23 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 23 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.3670-4540dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822790 | ||||||
| chr12:21822790
|
C | CAA | 14 | a0001c0001t0002g0033a0001c0001t0002g0078a0001c0001t0002g0126others(11): Show | 14 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.3670-4541_3670-454 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822790 | ||||||
| chr12:21822790
|
CAA | C | 10 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0157others(7): Show | 10 | HG01496.hp1 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.3670-4541_3670-454 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822790 | ||||||
| chr12:21822790
|
CAAA | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 38 | HG00408.hp1 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.3670-4542_3670-454 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21822790 | ||||||
| chr12:21823494
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.3670-5243G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21823494 | ||||||
| chr12:21823573
|
A | T | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3670-5322T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21823573 | ||||||
| chr12:21823870
|
C | A | 3 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0006t0005g0192 | 3 | HG02647.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3669+5088G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21823870 | ||||||
| chr12:21823954
|
G | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.3669+5004C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21823954 | ||||||
| chr12:21823965
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0205others(3): Show | 6 | HG02809.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3669+4993C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21823965 | ||||||
| chr12:21824001
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 77 | HG00408.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3669+4957A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824001 | ||||||
| chr12:21824122
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3669+4836C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824122 | ||||||
| chr12:21824203
|
G | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(24): Show | 28 | HG00621.hp1 HG00639.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.3669+4755C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824203 | ||||||
| chr12:21824238
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3669+4720T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824238 | ||||||
| chr12:21824390
|
T | G | 14 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0078others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3669+4568A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824390 | ||||||
| chr12:21824835
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(26): Show | 30 | HG00621.hp1 HG00639.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.3669+4123T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824835 | ||||||
| chr12:21824875
|
TTTCTC | T | 3 | a0001c0001t0005g0067a0001c0001t0011g0068a0001c0001t0011g0120 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3669+4078_3669+408 others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824875 | ||||||
| chr12:21824916
|
ATTTTGTT others(6): Show |
A | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(26): Show | 30 | HG00621.hp1 HG00639.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.3669+4029_3669+404 others(17): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824916 | ||||||
| chr12:21824945
|
T | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.3669+4013A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21824945 | ||||||
| chr12:21825066
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3669+3892T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825066 | ||||||
| chr12:21825164
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3669+3794C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825164 | ||||||
| chr12:21825176
|
C | T | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 25 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.3669+3782G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825176 | ||||||
| chr12:21825300
|
C | T | 2 | a0001c0001t0004g0127a0001c0001t0014g0071 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3669+3658G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825300 | ||||||
| chr12:21825304
|
A | G | 4 | a0001c0001t0005g0067a0001c0001t0011g0068a0001c0001t0011g0120others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3669+3654T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825304 | ||||||
| chr12:21825400
|
C | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3669+3558G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825400 | ||||||
| chr12:21825445
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.3669+3513T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825445 | ||||||
| chr12:21825519
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0090 | 2 | NA18612.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.3669+3439G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825519 | ||||||
| chr12:21825643
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3669+3315C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825643 | ||||||
| chr12:21825645
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3669+3313C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825645 | ||||||
| chr12:21825839
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3669+3119G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825839 | ||||||
| chr12:21825999
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(48): Show | 52 | HG00408.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.3669+2959T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21825999 | ||||||
| chr12:21826004
|
C | T | 1 | a0001c0004t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3669+2954G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826004 | ||||||
| chr12:21826266
|
A | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0102 | 2 | HG01261.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3669+2692T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826266 | ||||||
| chr12:21826280
|
T | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3669+2678A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826280 | ||||||
| chr12:21826352
|
C | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3669+2606G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826352 | ||||||
| chr12:21826573
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3669+2385G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826573 | ||||||
| chr12:21826889
|
T | G | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3669+2069A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21826889 | ||||||
| chr12:21827054
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3669+1904C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827054 | ||||||
| chr12:21827108
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3669+1850C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827108 | ||||||
| chr12:21827257
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3669+1701A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827257 | ||||||
| chr12:21827285
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3669+1673G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827285 | ||||||
| chr12:21827527
|
A | AAC | 50 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 50 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.3669+1429_3669+143 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
A | AACAC | 22 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0019others(19): Show | 22 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.3669+1427_3669+143 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
A | AACACAC | 14 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0045others(11): Show | 14 | HG00621.hp2 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3669+1425_3669+143 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
A | AACACACA others(1): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0201 | 2 | HG01891.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3669+1423_3669+143 others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0055 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3669+1419_3669+143 others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AAC | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0060others(15): Show | 18 | HG01175.hp2 HG01516.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3669+1429_3669+143 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACAC | A | 10 | a0001c0001t0001g0052a0001c0001t0001g0084a0001c0001t0001g0085others(7): Show | 10 | HG00140.hp1 HG01074.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3669+1427_3669+143 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACAC | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3669+1425_3669+143 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACACA others(1): Show |
A | 5 | a0001c0001t0001g0130a0001c0001t0001g0200a0001c0001t0002g0202others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3669+1423_3669+143 others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACACA others(3): Show |
A | 15 | a0001c0001t0002g0033a0001c0001t0002g0078a0001c0001t0002g0126others(12): Show | 15 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.3669+1421_3669+143 others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACACA others(5): Show |
A | 3 | a0001c0001t0002g0043a0001c0003t0016g0173a0001c0006t0005g0192 | 3 | HG02572.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3669+1419_3669+143 others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACACA others(7): Show |
A | 25 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(22): Show | 26 | HG00621.hp1 HG00639.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.3669+1417_3669+143 others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827527
|
AACACACA others(11): Show |
A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3669+1413_3669+143 others(22): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827527 | ||||||
| chr12:21827558
|
ACACACAC others(7): Show |
A | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3669+1386_3669+139 others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827558 | ||||||
| chr12:21827572
|
T | G | 8 | a0001c0001t0002g0033a0001c0001t0002g0078a0001c0001t0002g0126others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3669+1386A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827572 | ||||||
| chr12:21827602
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.3669+1356C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827602 | ||||||
| chr12:21827684
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(40): Show | 44 | HG00621.hp1 HG00639.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.3669+1274A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827684 | ||||||
| chr12:21827886
|
T | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(65): Show | 69 | HG00408.hp1 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3669+1072A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21827886 | ||||||
| chr12:21828186
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3669+772C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21828186 | ||||||
| chr12:21828189
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3669+769G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21828189 | ||||||
| chr12:21828291
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(76): Show | 80 | HG00408.hp1 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.3669+667T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21828291 | ||||||
| chr12:21828433
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3669+525G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21828433 | ||||||
| chr12:21828918
|
T | C | 3 | a0001c0001t0019g0196a0001c0002t0023g0182a0001c0006t0005g0192 | 3 | HG02647.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3669+40A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 31/39 | chr12 | 21828918 | ||||||
| chr12:21829191
|
C | CT | 82 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0014others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.3567-132dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829191 | ||||||
| chr12:21829191
|
C | CTT | 22 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0088others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(19): Show |
intron_variant | MODIFIER | c.3567-133_3567-132d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829191 | ||||||
| chr12:21829191
|
CTTTT | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 18 | HG00408.hp1 HG01993.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.3567-135_3567-132d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829191 | ||||||
| chr12:21829191
|
CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0002g0033a0001c0001t0002g0078a0001c0001t0002g0126others(10): Show | 13 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.3567-140_3567-132d others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829191 | ||||||
| chr12:21829191
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3567-143_3567-132d others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829191 | ||||||
| chr12:21829196
|
T | C | 1 | a0001c0009t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3567-136A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829196 | ||||||
| chr12:21829219
|
T | TC | 3 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0004t0001g0119 | 3 | HG01891.hp1 HG02486.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3567-160dupG | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829219 | ||||||
| chr12:21829240
|
T | C | 2 | a0001c0001t0001g0041a0001c0006t0001g0191 | 2 | HG01346.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3567-180A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829240 | ||||||
| chr12:21829241
|
G | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3567-181C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829241 | ||||||
| chr12:21829257
|
A | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0115 | 2 | HG01175.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.3567-197T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829257 | ||||||
| chr12:21829263
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3567-203C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829263 | ||||||
| chr12:21829270
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02129.hp2 NA18960.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.3567-210G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829270 | ||||||
| chr12:21829324
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3567-264G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829324 | ||||||
| chr12:21829346
|
C | T | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3567-286G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829346 | ||||||
| chr12:21829347
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(53): Show | 57 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.3567-287T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829347 | ||||||
| chr12:21829392
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0153 | 2 | HG03209.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3567-332C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829392 | ||||||
| chr12:21829393
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3567-333T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829393 | ||||||
| chr12:21829415
|
A | G | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3567-355T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829415 | ||||||
| chr12:21829418
|
G | A | 11 | a0001c0001t0001g0174a0001c0001t0002g0033a0001c0001t0002g0078others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3567-358C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829418 | ||||||
| chr12:21829423
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0080 | 2 | HG02976.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3567-363C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829423 | ||||||
| chr12:21829423
|
G | C | 3 | a0001c0001t0005g0067a0001c0001t0011g0068a0001c0001t0011g0120 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3567-363C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829423 | ||||||
| chr12:21829426
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0159 | 2 | HG01175.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.3567-366G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829426 | ||||||
| chr12:21829436
|
T | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0123a0001c0001t0001g0148others(1): Show | 4 | HG00280.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.3567-376A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829436 | ||||||
| chr12:21829444
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3567-384C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829444 | ||||||
| chr12:21829448
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0123a0001c0001t0001g0148others(1): Show | 4 | HG00280.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.3567-388T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829448 | ||||||
| chr12:21829452
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0123a0001c0001t0001g0148 | 3 | HG03491.hp1 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3567-392A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829452 | ||||||
| chr12:21829484
|
T | A | 29 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(26): Show | 29 | HG00323.hp2 HG01175.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.3567-424A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829484 | ||||||
| chr12:21829490
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0005g0067 | 2 | HG03209.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3567-430G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829490 | ||||||
| chr12:21829491
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3567-431C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829491 | ||||||
| chr12:21829493
|
A | G | 11 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0099others(8): Show | 11 | HG00323.hp2 HG01346.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.3567-433T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829493 | ||||||
| chr12:21829493
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3567-433T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829493 | ||||||
| chr12:21829497
|
G | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3567-437C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829497 | ||||||
| chr12:21829509
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.3567-449T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829509 | ||||||
| chr12:21829656
|
T | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0048others(14): Show | 18 | HG00639.hp2 HG01106.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.3567-596A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829656 | ||||||
| chr12:21829663
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3567-603G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829663 | ||||||
| chr12:21829665
|
A | T | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3567-605T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829665 | ||||||
| chr12:21829666
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3567-606G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829666 | ||||||
| chr12:21829760
|
C | T | 1 | a0001c0001t0024g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3567-700G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829760 | ||||||
| chr12:21829893
|
T | G | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3567-833A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829893 | ||||||
| chr12:21829971
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3567-911C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829971 | ||||||
| chr12:21829986
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 40 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.3567-926G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21829986 | ||||||
| chr12:21830004
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3567-944A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830004 | ||||||
| chr12:21830051
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3567-991G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830051 | ||||||
| chr12:21830181
|
C | T | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567-1121G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830181 | ||||||
| chr12:21830240
|
T | C | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3567-1180A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830240 | ||||||
| chr12:21830635
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3567-1575G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830635 | ||||||
| chr12:21830699
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3567-1639C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830699 | ||||||
| chr12:21830727
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3567-1667T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830727 | ||||||
| chr12:21830763
|
C | T | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3567-1703G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830763 | ||||||
| chr12:21830906
|
C | G | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3567-1846G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830906 | ||||||
| chr12:21830974
|
T | TTATC | 47 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(44): Show | 47 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.3567-1918_3567-191 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21830974
|
T | TTATCTAT others(1): Show |
67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 68 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.3567-1922_3567-191 others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21830974
|
T | TTATCTAT others(5): Show |
34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0041others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3567-1926_3567-191 others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21830974
|
T | TTATCTAT others(9): Show |
8 | a0001c0001t0001g0045a0001c0001t0001g0102a0001c0001t0001g0112others(5): Show | 8 | HG00323.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.3567-1930_3567-191 others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21830974
|
TTATC | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.3567-1918_3567-191 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21830974
|
TTATCTAT others(5): Show |
T | 14 | a0001c0001t0001g0174a0001c0001t0002g0033a0001c0001t0002g0078others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3567-1926_3567-191 others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21830974 | ||||||
| chr12:21831055
|
A | AT | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.3567-1996dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831055 | ||||||
| chr12:21831137
|
T | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.3567-2077A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831137 | ||||||
| chr12:21831362
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 16 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.3567-2302G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831362 | ||||||
| chr12:21831549
|
C | T | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3567-2489G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831549 | ||||||
| chr12:21831716
|
G | T | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3567-2656C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831716 | ||||||
| chr12:21831767
|
G | A | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3567-2707C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831767 | ||||||
| chr12:21831777
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3567-2717G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831777 | ||||||
| chr12:21831837
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3567-2777C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21831837 | ||||||
| chr12:21832036
|
A | C | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.3567-2976T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832036 | ||||||
| chr12:21832072
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.3567-3012G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832072 | ||||||
| chr12:21832159
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0079 | 3 | HG01884.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3567-3099A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832159 | ||||||
| chr12:21832288
|
G | A | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567-3228C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832288 | ||||||
| chr12:21832289
|
C | T | 1 | a0001c0001t0024g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3567-3229G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832289 | ||||||
| chr12:21832359
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.3567-3299A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832359 | ||||||
| chr12:21832359
|
T | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0147 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3567-3299A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832359 | ||||||
| chr12:21832464
|
A | G | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567-3404T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832464 | ||||||
| chr12:21832479
|
C | A | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567-3419G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832479 | ||||||
| chr12:21832682
|
A | T | 1 | a0001c0001t0005g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3567-3622T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832682 | ||||||
| chr12:21832746
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3567-3686T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832746 | ||||||
| chr12:21832821
|
A | C | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3567-3761T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832821 | ||||||
| chr12:21832953
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG02027.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3567-3893G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21832953 | ||||||
| chr12:21833144
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3567-4084C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21833144 | ||||||
| chr12:21833432
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3567-4372C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21833432 | ||||||
| chr12:21833517
|
A | T | 1 | a0001c0001t0005g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3567-4457T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21833517 | ||||||
| chr12:21833794
|
T | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0070others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3566+4284A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21833794 | ||||||
| chr12:21834102
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3566+3976T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834102 | ||||||
| chr12:21834190
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3566+3888T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834190 | ||||||
| chr12:21834313
|
G | T | 1 | a0001c0001t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3566+3765C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834313 | ||||||
| chr12:21834498
|
A | G | 1 | a0004c0011t0001g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3566+3580T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834498 | ||||||
| chr12:21834588
|
G | A | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3566+3490C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834588 | ||||||
| chr12:21834670
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3566+3408G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834670 | ||||||
| chr12:21834687
|
A | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG01175.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3566+3391T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834687 | ||||||
| chr12:21834744
|
G | GAT | 5 | a0001c0001t0001g0093a0001c0001t0001g0130a0001c0001t0001g0200others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3566+3332_3566+333 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834744 | ||||||
| chr12:21834783
|
T | TTA | 38 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0024others(35): Show | 38 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.3566+3293_3566+329 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834783 | ||||||
| chr12:21834784
|
T | TACACAC | 2 | a0001c0001t0001g0108a0001c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3566+3293_3566+329 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834784 | ||||||
| chr12:21834784
|
TATACACA others(7): Show |
T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3566+3280_3566+329 others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834784 | ||||||
| chr12:21834786
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3566+3292A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TAC | 4 | a0001c0001t0001g0048a0001c0001t0001g0174a0001c0001t0004g0127others(1): Show | 4 | HG02145.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3566+3290_3566+329 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TACAC | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(29): Show | 33 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.3566+3288_3566+329 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TACACAC | 3 | a0001c0001t0001g0098a0001c0001t0001g0116a0001c0001t0001g0118 | 3 | HG01981.hp2 HG02027.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3566+3286_3566+329 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3566+3282_3566+329 others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TATAC | 16 | a0001c0001t0001g0014a0001c0001t0001g0058a0001c0001t0001g0061others(13): Show | 16 | HG00280.hp1 HG00738.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.3566+3291_3566+329 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TATACAC | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.3566+3291_3566+329 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TATACACA others(1): Show |
9 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0080others(6): Show | 9 | HG01346.hp2 HG01433.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.3566+3291_3566+329 others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TATACACA others(3): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0083a0001c0001t0001g0103others(2): Show | 5 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3566+3291_3566+329 others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
T | TATACACA others(5): Show |
1 | a0001c0001t0001g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3566+3291_3566+329 others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
TAC | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.3566+3290_3566+329 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
TACAC | T | 18 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0082others(15): Show | 18 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.3566+3288_3566+329 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
TACACAC | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG00408.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3566+3286_3566+329 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3566+3282_3566+329 others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834786
|
TACACACA others(7): Show |
T | 2 | a0001c0003t0007g0180a0001c0003t0007g0204 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3566+3278_3566+329 others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834786 | ||||||
| chr12:21834788
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0155a0001c0001t0020g0140 | 3 | HG01993.hp1 HG02293.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3566+3290G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834788 | ||||||
| chr12:21834790
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0130others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3566+3288G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834790 | ||||||
| chr12:21834792
|
C | T | 15 | a0001c0001t0001g0057a0001c0001t0001g0082a0001c0001t0001g0084others(12): Show | 15 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.3566+3286G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834792 | ||||||
| chr12:21834794
|
C | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG00408.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3566+3284G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834794 | ||||||
| chr12:21834798
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3566+3280G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834798 | ||||||
| chr12:21834956
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3566+3122C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21834956 | ||||||
| chr12:21835007
|
G | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3566+3071C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835007 | ||||||
| chr12:21835013
|
C | A | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.3566+3065G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835013 | ||||||
| chr12:21835153
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3566+2925T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835153 | ||||||
| chr12:21835154
|
T | G | 19 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0082others(16): Show | 19 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3566+2924A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835154 | ||||||
| chr12:21835237
|
T | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3566+2841A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835237 | ||||||
| chr12:21835274
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3566+2804T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835274 | ||||||
| chr12:21835292
|
A | G | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3566+2786T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835292 | ||||||
| chr12:21835329
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3566+2749G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835329 | ||||||
| chr12:21835452
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2626G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835452 | ||||||
| chr12:21835471
|
C | T | 1 | a0002c0007t0001g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3566+2607G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835471 | ||||||
| chr12:21835482
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3566+2596C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835482 | ||||||
| chr12:21835536
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2542G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835536 | ||||||
| chr12:21835553
|
C | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2525G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835553 | ||||||
| chr12:21835560
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2518G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835560 | ||||||
| chr12:21835599
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2479G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835599 | ||||||
| chr12:21835646
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2432G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835646 | ||||||
| chr12:21835648
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3566+2430G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835648 | ||||||
| chr12:21835730
|
G | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3566+2348C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835730 | ||||||
| chr12:21835732
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3566+2346T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835732 | ||||||
| chr12:21835735
|
C | G | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.3566+2343G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835735 | ||||||
| chr12:21835854
|
C | A | 1 | a0002c0007t0001g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3566+2224G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835854 | ||||||
| chr12:21835866
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3566+2212G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835866 | ||||||
| chr12:21835919
|
C | G | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3566+2159G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21835919 | ||||||
| chr12:21836059
|
C | G | 1 | a0001c0002t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3566+2019G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836059 | ||||||
| chr12:21836168
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0103 | 2 | HG01516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3566+1910G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836168 | ||||||
| chr12:21836328
|
C | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.3566+1750G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836328 | ||||||
| chr12:21836387
|
G | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.3566+1691C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836387 | ||||||
| chr12:21836420
|
C | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3566+1658G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836420 | ||||||
| chr12:21836596
|
T | A | 3 | a0001c0001t0005g0067a0001c0001t0011g0068a0001c0001t0011g0120 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3566+1482A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836596 | ||||||
| chr12:21836685
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0168 | 2 | HG02486.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3566+1393C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836685 | ||||||
| chr12:21836723
|
C | T | 2 | a0001c0005t0001g0006a0001c0005t0001g0016 | 2 | NA18981.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3566+1355G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836723 | ||||||
| chr12:21836754
|
T | C | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3566+1324A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21836754 | ||||||
| chr12:21837033
|
G | A | 1 | a0002c0007t0001g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3566+1045C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837033 | ||||||
| chr12:21837177
|
C | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3566+901G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837177 | ||||||
| chr12:21837269
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0005g0067a0001c0001t0019g0196others(3): Show | 6 | HG01496.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3566+809G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837269 | ||||||
| chr12:21837431
|
C | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.3566+647G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837431 | ||||||
| chr12:21837449
|
T | A | 3 | a0001c0001t0005g0067a0001c0001t0011g0068a0001c0001t0011g0120 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3566+629A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837449 | ||||||
| chr12:21837467
|
T | C | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3566+611A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837467 | ||||||
| chr12:21837588
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3566+490G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837588 | ||||||
| chr12:21837734
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0019g0196a0002c0007t0001g0039 | 3 | HG01496.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3566+344G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837734 | ||||||
| chr12:21837779
|
AT | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3566+298delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837779 | ||||||
| chr12:21837811
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3566+267C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 30/39 | chr12 | 21837811 | ||||||
| chr12:21838241
|
A | G | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3474-71T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21838241 | ||||||
| chr12:21838263
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0019g0196 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3474-93A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21838263 | ||||||
| chr12:21838686
|
A | G | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.3474-516T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21838686 | ||||||
| chr12:21838819
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3474-649T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21838819 | ||||||
| chr12:21838966
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 40 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.3474-796T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21838966 | ||||||
| chr12:21839018
|
G | A | 1 | a0001c0003t0007g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3474-848C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839018 | ||||||
| chr12:21839061
|
G | A | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3474-891C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839061 | ||||||
| chr12:21839190
|
C | G | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.3474-1020G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839190 | ||||||
| chr12:21839245
|
A | G | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3474-1075T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839245 | ||||||
| chr12:21839363
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3474-1193C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839363 | ||||||
| chr12:21839381
|
T | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3474-1211A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839381 | ||||||
| chr12:21839392
|
G | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(44): Show | 47 | HG00280.hp2 HG00408.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.3474-1222C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839392 | ||||||
| chr12:21839621
|
A | G | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3474-1451T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839621 | ||||||
| chr12:21839784
|
C | A | 1 | a0001c0001t0003g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3474-1614G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839784 | ||||||
| chr12:21839810
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3474-1640G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839810 | ||||||
| chr12:21839876
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3474-1706C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839876 | ||||||
| chr12:21839887
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3474-1717T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21839887 | ||||||
| chr12:21840046
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3474-1876C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840046 | ||||||
| chr12:21840056
|
T | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3474-1886A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840056 | ||||||
| chr12:21840206
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3474-2036G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840206 | ||||||
| chr12:21840307
|
C | G | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3473+2007G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840307 | ||||||
| chr12:21840338
|
T | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3473+1976A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840338 | ||||||
| chr12:21840376
|
G | A | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3473+1938C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840376 | ||||||
| chr12:21840448
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3473+1866G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840448 | ||||||
| chr12:21840544
|
G | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3473+1770C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840544 | ||||||
| chr12:21840598
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3473+1716C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840598 | ||||||
| chr12:21840686
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 58 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.3473+1628C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840686 | ||||||
| chr12:21840755
|
A | G | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0006t0001g0191 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3473+1559T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840755 | ||||||
| chr12:21840987
|
C | T | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3473+1327G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21840987 | ||||||
| chr12:21841104
|
A | C | 2 | a0001c0001t0001g0024a0001c0003t0016g0173 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3473+1210T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841104 | ||||||
| chr12:21841177
|
A | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3473+1137T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841177 | ||||||
| chr12:21841342
|
GTTTCC | G | 5 | a0001c0001t0001g0157a0001c0003t0007g0180a0001c0003t0007g0204others(2): Show | 5 | HG01496.hp1 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3473+967_3473+971d others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841342
|
GTTTCCT | G | 8 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0132others(5): Show | 8 | HG01168.hp1 HG01261.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.3473+966_3473+971d others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841342
|
GTTTCCTT | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.3473+965_3473+971d others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841342
|
GTTTCCTT others(1): Show |
G | 5 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0138others(2): Show | 5 | HG02132.hp1 HG03041.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.3473+964_3473+971d others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841342
|
GTTTCCTT others(2): Show |
G | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(23): Show | 26 | HG00408.hp1 HG01884.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.3473+963_3473+971d others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841342
|
GTTTCCTT others(3): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3473+962_3473+971d others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841342 | ||||||
| chr12:21841347
|
C | CT | 9 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0118others(6): Show | 9 | HG01106.hp1 HG01106.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.3473+966dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841347 | ||||||
| chr12:21841347
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3473+967G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841347 | ||||||
| chr12:21841347
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0006t0001g0191 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3473+956_3473+966d others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841347 | ||||||
| chr12:21841347
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0079a0001c0001t0005g0067 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3473+955_3473+966d others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841347 | ||||||
| chr12:21841347
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3473+954_3473+966d others(15): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841347 | ||||||
| chr12:21841352
|
T | C | 5 | a0001c0001t0001g0157a0001c0003t0007g0180a0001c0003t0007g0204others(2): Show | 5 | HG01496.hp1 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3473+962A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841352 | ||||||
| chr12:21841353
|
T | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0132others(5): Show | 8 | HG01168.hp1 HG01261.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.3473+961A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841353 | ||||||
| chr12:21841354
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.3473+960A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841354 | ||||||
| chr12:21841355
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0138others(2): Show | 5 | HG02132.hp1 HG03041.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.3473+959A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841355 | ||||||
| chr12:21841356
|
T | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(23): Show | 26 | HG00408.hp1 HG01884.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.3473+958A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841356 | ||||||
| chr12:21841357
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3473+957A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841357 | ||||||
| chr12:21841360
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3473+954A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841360 | ||||||
| chr12:21841397
|
C | G | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.3473+917G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841397 | ||||||
| chr12:21841451
|
C | T | 1 | a0001c0002t0004g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3473+863G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841451 | ||||||
| chr12:21841600
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3473+714C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841600 | ||||||
| chr12:21841749
|
G | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3473+565C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841749 | ||||||
| chr12:21841860
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3473+454T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841860 | ||||||
| chr12:21841972
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3473+342A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21841972 | ||||||
| chr12:21842021
|
G | C | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3473+293C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21842021 | ||||||
| chr12:21842098
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3473+216T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21842098 | ||||||
| chr12:21842132
|
C | T | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3473+182G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21842132 | ||||||
| chr12:21842202
|
G | A | 3 | a0001c0001t0001g0157a0001c0003t0009g0209a0001c0003t0016g0173 | 3 | HG01496.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3473+112C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21842202 | ||||||
| chr12:21842218
|
C | T | 1 | a0001c0001t0003g0147 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3473+96G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 29/39 | chr12 | 21842218 | ||||||
| chr12:21842621
|
C | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.3316-150G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21842621 | ||||||
| chr12:21842872
|
A | C | 1 | a0001c0001t0001g0010 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3316-401T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21842872 | ||||||
| chr12:21843111
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3316-640A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843111 | ||||||
| chr12:21843317
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3316-846G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843317 | ||||||
| chr12:21843475
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3316-1004T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843475 | ||||||
| chr12:21843512
|
T | C | 1 | a0001c0002t0004g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3315+971A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843512 | ||||||
| chr12:21843552
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3315+931A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843552 | ||||||
| chr12:21843600
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3315+883T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843600 | ||||||
| chr12:21843703
|
A | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 33 | HG00408.hp1 HG01496.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.3315+780T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843703 | ||||||
| chr12:21843814
|
T | G | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3315+669A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21843814 | ||||||
| chr12:21844032
|
A | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3315+451T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21844032 | ||||||
| chr12:21844187
|
G | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.3315+296C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21844187 | ||||||
| chr12:21844293
|
CTGAGT | C | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3315+185_3315+189d others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21844293 | ||||||
| chr12:21844391
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0005g0067 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3315+92T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 28/39 | chr12 | 21844391 | ||||||
| chr12:21844648
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3246-96A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 27/39 | chr12 | 21844648 | ||||||
| chr12:21844742
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3245+25C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 27/39 | chr12 | 21844742 | ||||||
| chr12:21844744
|
G | T | 1 | a0001c0001t0003g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3245+23C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 27/39 | chr12 | 21844744 | ||||||
| chr12:21844940
|
C | T | 14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3097-25G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21844940 | ||||||
| chr12:21844998
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3097-83T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21844998 | ||||||
| chr12:21845008
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01993.hp1 HG02293.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.3097-93A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845008 | ||||||
| chr12:21845078
|
C | T | 14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3097-163G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845078 | ||||||
| chr12:21845137
|
C | CT | 121 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3097-223dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845137 | ||||||
| chr12:21845140
|
A | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3097-225T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845140 | ||||||
| chr12:21845211
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3097-296G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845211 | ||||||
| chr12:21845297
|
A | C | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3096+306T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845297 | ||||||
| chr12:21845348
|
ACT | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0022g0018 | 3 | HG00280.hp1 HG01516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3096+253_3096+254d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845348 | ||||||
| chr12:21845503
|
T | A | 2 | a0001c0001t0001g0200a0001c0001t0009g0129 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3096+100A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845503 | ||||||
| chr12:21845504
|
A | G | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3096+99T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845504 | ||||||
| chr12:21845559
|
A | C | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3096+44T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845559 | ||||||
| chr12:21845563
|
T | G | 1 | a0003c0012t0001g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3096+40A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 26/39 | chr12 | 21845563 | ||||||
| chr12:21846174
|
T | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2867-342A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846174 | ||||||
| chr12:21846361
|
G | C | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2867-529C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846361 | ||||||
| chr12:21846473
|
T | C | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2867-641A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846473 | ||||||
| chr12:21846540
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2867-708T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846540 | ||||||
| chr12:21846685
|
G | C | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2867-853C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846685 | ||||||
| chr12:21846929
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2867-1097G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846929 | ||||||
| chr12:21846944
|
C | G | 10 | a0001c0001t0001g0079a0001c0001t0005g0067a0001c0001t0008g0188others(7): Show | 10 | HG01884.hp1 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.2867-1112G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21846944 | ||||||
| chr12:21847066
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2866+1084G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847066 | ||||||
| chr12:21847083
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2866+1067A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847083 | ||||||
| chr12:21847122
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2866+1028T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847122 | ||||||
| chr12:21847336
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2866+814A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847336 | ||||||
| chr12:21847369
|
T | C | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2866+781A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847369 | ||||||
| chr12:21847444
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2866+706T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847444 | ||||||
| chr12:21847459
|
G | GT | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2866+690dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847459 | ||||||
| chr12:21847675
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2866+475T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847675 | ||||||
| chr12:21847687
|
ATTCTAAT others(1): Show |
A | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2866+455_2866+462d others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847687 | ||||||
| chr12:21847707
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2866+443G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847707 | ||||||
| chr12:21847856
|
A | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2866+294T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847856 | ||||||
| chr12:21847979
|
A | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0041 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2866+171T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21847979 | ||||||
| chr12:21848088
|
T | TA | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2866+61dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 25/39 | chr12 | 21848088 | ||||||
| chr12:21848338
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0073a0001c0001t0001g0102 | 3 | HG00639.hp2 HG01261.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2770-92G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848338 | ||||||
| chr12:21848356
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2770-110C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848356 | ||||||
| chr12:21848438
|
G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(5): Show | 8 | HG02258.hp2 HG02630.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2770-192C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848438 | ||||||
| chr12:21848496
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2770-250T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848496 | ||||||
| chr12:21848835
|
A | AGGAGGGA others(17): Show |
1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2770-590_2770-589i others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848835 | ||||||
| chr12:21848949
|
C | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2770-703G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21848949 | ||||||
| chr12:21849176
|
T | C | 2 | a0001c0001t0004g0127a0001c0002t0004g0183 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2770-930A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849176 | ||||||
| chr12:21849182
|
G | GA | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2770-937dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849182 | ||||||
| chr12:21849218
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2770-972T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849218 | ||||||
| chr12:21849235
|
T | C | 1 | a0001c0002t0004g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2770-989A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849235 | ||||||
| chr12:21849254
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2770-1008C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849254 | ||||||
| chr12:21849277
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2770-1031C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849277 | ||||||
| chr12:21849312
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2770-1066T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849312 | ||||||
| chr12:21849608
|
TAAAC | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0060a0001c0001t0001g0066others(1): Show | 4 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-1366_2770-136 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849608 | ||||||
| chr12:21849634
|
C | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2770-1388G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21849634 | ||||||
| chr12:21850106
|
C | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770-1860G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850106 | ||||||
| chr12:21850259
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2769+1838G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850259 | ||||||
| chr12:21850610
|
G | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.2769+1487C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850610 | ||||||
| chr12:21850663
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2769+1434A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850663 | ||||||
| chr12:21850727
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.2769+1370C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850727 | ||||||
| chr12:21850788
|
C | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.2769+1309G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850788 | ||||||
| chr12:21850793
|
C | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2769+1304G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21850793 | ||||||
| chr12:21851053
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2769+1044G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851053 | ||||||
| chr12:21851264
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.2769+833C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851264 | ||||||
| chr12:21851347
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0053others(13): Show | 17 | HG00639.hp2 HG01106.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.2769+750G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851347 | ||||||
| chr12:21851501
|
G | A | 7 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0001g0184others(4): Show | 7 | HG02055.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2769+596C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851501 | ||||||
| chr12:21851652
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2769+445G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851652 | ||||||
| chr12:21851696
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2769+401A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851696 | ||||||
| chr12:21851721
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2769+376C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851721 | ||||||
| chr12:21851902
|
GC | G | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2769+194delG | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851902 | ||||||
| chr12:21851932
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2769+165A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21851932 | ||||||
| chr12:21852051
|
C | T | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2769+46G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21852051 | ||||||
| chr12:21852069
|
T | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.2769+28A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 24/39 | chr12 | 21852069 | ||||||
| chr12:21852233
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0168 | 2 | HG02486.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2644-11G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/39 | chr12 | 21852233 | ||||||
| chr12:21852241
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2644-19G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/39 | chr12 | 21852241 | ||||||
| chr12:21852260
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2644-38C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/39 | chr12 | 21852260 | ||||||
| chr12:21852324
|
G | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0193 | 3 | HG00140.hp1 HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2643+44C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/39 | chr12 | 21852324 | ||||||
| chr12:21852351
|
C | G | 1 | a0003c0012t0001g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2643+17G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 23/39 | chr12 | 21852351 | ||||||
| chr12:21852536
|
C | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2506-31G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852536 | ||||||
| chr12:21852576
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2506-71T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852576 | ||||||
| chr12:21852837
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2506-332T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852837 | ||||||
| chr12:21852847
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.2506-342T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852847 | ||||||
| chr12:21852885
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0043 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2506-380T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852885 | ||||||
| chr12:21852931
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2506-426C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21852931 | ||||||
| chr12:21853042
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2506-537A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853042 | ||||||
| chr12:21853140
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2506-635G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853140 | ||||||
| chr12:21853167
|
A | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2506-662T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853167 | ||||||
| chr12:21853182
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 52 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2506-677G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853182 | ||||||
| chr12:21853230
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0080others(5): Show | 8 | HG02258.hp2 HG02630.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2506-725G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853230 | ||||||
| chr12:21853336
|
A | T | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2506-831T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853336 | ||||||
| chr12:21853434
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2506-929T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853434 | ||||||
| chr12:21853435
|
G | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.2506-930C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853435 | ||||||
| chr12:21853460
|
C | CTAT | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2506-958_2506-956d others(5): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853460 | ||||||
| chr12:21853562
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2506-1057T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853562 | ||||||
| chr12:21853729
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2506-1224C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853729 | ||||||
| chr12:21853912
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2506-1407A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21853912 | ||||||
| chr12:21854184
|
T | G | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2506-1679A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854184 | ||||||
| chr12:21854333
|
G | T | 1 | a0001c0001t0009g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2506-1828C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854333 | ||||||
| chr12:21854653
|
A | G | 1 | a0001c0005t0001g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2506-2148T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854653 | ||||||
| chr12:21854748
|
T | C | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2506-2243A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854748 | ||||||
| chr12:21854969
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2506-2464G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854969 | ||||||
| chr12:21854978
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2506-2473T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21854978 | ||||||
| chr12:21855010
|
A | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 22 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.2506-2505T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855010 | ||||||
| chr12:21855093
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0047 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2506-2588G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855093 | ||||||
| chr12:21855225
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2506-2720T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855225 | ||||||
| chr12:21855368
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2506-2863G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855368 | ||||||
| chr12:21855377
|
G | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2506-2872C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855377 | ||||||
| chr12:21855416
|
T | A | 1 | a0001c0001t0024g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2506-2911A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855416 | ||||||
| chr12:21855433
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2506-2928C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855433 | ||||||
| chr12:21855464
|
T | G | 12 | a0001c0001t0001g0079a0001c0001t0001g0157a0001c0001t0004g0023others(9): Show | 12 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2506-2959A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855464 | ||||||
| chr12:21855556
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0114 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2506-3051C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855556 | ||||||
| chr12:21855802
|
A | G | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.2506-3297T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21855802 | ||||||
| chr12:21856007
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2506-3502T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856007 | ||||||
| chr12:21856043
|
A | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0004g0183 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2506-3538T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856043 | ||||||
| chr12:21856128
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2505+3458T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856128 | ||||||
| chr12:21856397
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0004g0183 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2505+3189A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856397 | ||||||
| chr12:21856461
|
A | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(24): Show | 27 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.2505+3125T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856461 | ||||||
| chr12:21856513
|
A | AT | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2505+3072dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856513 | ||||||
| chr12:21856773
|
A | C | 15 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0174others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2505+2813T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856773 | ||||||
| chr12:21856882
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2505+2704A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856882 | ||||||
| chr12:21856892
|
T | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2505+2694A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856892 | ||||||
| chr12:21856948
|
C | T | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2505+2638G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21856948 | ||||||
| chr12:21857039
|
T | C | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0006t0001g0191 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2505+2547A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857039 | ||||||
| chr12:21857247
|
G | A | 8 | a0001c0001t0001g0079a0001c0001t0004g0023a0001c0001t0004g0127others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2505+2339C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857247 | ||||||
| chr12:21857498
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2505+2088C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857498 | ||||||
| chr12:21857716
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2505+1870C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857716 | ||||||
| chr12:21857731
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2505+1855C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857731 | ||||||
| chr12:21857899
|
C | T | 1 | a0004c0011t0001g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2505+1687G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21857899 | ||||||
| chr12:21858262
|
G | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2505+1324C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21858262 | ||||||
| chr12:21858298
|
G | T | 1 | a0001c0009t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2505+1288C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21858298 | ||||||
| chr12:21858578
|
CA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2505+1007delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21858578 | ||||||
| chr12:21858739
|
C | T | 141 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2505+847G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21858739 | ||||||
| chr12:21859015
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2505+571C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859015 | ||||||
| chr12:21859134
|
A | G | 3 | a0001c0001t0004g0199a0002c0007t0001g0039a0002c0007t0001g0049 | 3 | HG02145.hp2 HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2505+452T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859134 | ||||||
| chr12:21859262
|
T | A | 1 | a0001c0003t0016g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2505+324A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859262 | ||||||
| chr12:21859413
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.2505+173C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859413 | ||||||
| chr12:21859488
|
C | T | 6 | a0001c0001t0001g0051a0001c0001t0001g0117a0001c0001t0001g0136others(3): Show | 6 | HG00323.hp2 NA18947.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2505+98G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859488 | ||||||
| chr12:21859489
|
C | T | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2505+97G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 22/39 | chr12 | 21859489 | ||||||
| chr12:21860091
|
T | TA | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.2425-426dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860091 | ||||||
| chr12:21860279
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0053others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2425-613T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860279 | ||||||
| chr12:21860339
|
A | T | 1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2424+632T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860339 | ||||||
| chr12:21860407
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0160 | 2 | HG02132.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2424+564G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860407 | ||||||
| chr12:21860468
|
A | G | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2424+503T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860468 | ||||||
| chr12:21860561
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2424+410A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860561 | ||||||
| chr12:21860962
|
A | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2424+9T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 21/39 | chr12 | 21860962 | ||||||
| chr12:21861223
|
T | C | 2 | a0001c0002t0023g0182a0001c0006t0005g0192 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2340-168A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861223 | ||||||
| chr12:21861226
|
C | CA | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2340-172_2340-171i others(3): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861226 | ||||||
| chr12:21861227
|
C | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2340-172G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861227 | ||||||
| chr12:21861228
|
C | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2340-173G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861228 | ||||||
| chr12:21861229
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2340-174G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861229 | ||||||
| chr12:21861230
|
C | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2340-175G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861230 | ||||||
| chr12:21861230
|
C | CAT | 14 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0066others(11): Show | 14 | HG01346.hp2 HG02132.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2340-176_2340-175i others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861230 | ||||||
| chr12:21861231
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2340-176G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861231 | ||||||
| chr12:21861231
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2340-176G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861231 | ||||||
| chr12:21861241
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2340-186A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861241 | ||||||
| chr12:21861288
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2340-233A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861288 | ||||||
| chr12:21861437
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2340-382C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861437 | ||||||
| chr12:21861539
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.2340-484C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861539 | ||||||
| chr12:21861946
|
A | T | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2340-891T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21861946 | ||||||
| chr12:21862088
|
T | C | 141 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2339+865A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862088 | ||||||
| chr12:21862140
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG00408.hp1 HG02129.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2339+813G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862140 | ||||||
| chr12:21862141
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0019g0196a0001c0003t0009g0209 | 3 | HG01884.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2339+812C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862141 | ||||||
| chr12:21862180
|
A | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.2339+773T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862180 | ||||||
| chr12:21862580
|
ATTC | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2339+370_2339+372d others(5): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862580 | ||||||
| chr12:21862834
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2339+119C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 20/39 | chr12 | 21862834 | ||||||
| chr12:21863070
|
GA | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2238-17delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863070 | ||||||
| chr12:21863282
|
AAGTTTGG others(39): Show |
A | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2238-274_2238-229d others(48): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863282 | ||||||
| chr12:21863284
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(87): Show | 90 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2238-230C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863284 | ||||||
| chr12:21863454
|
GA | G | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2238-401delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863454 | ||||||
| chr12:21863469
|
T | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2238-415A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863469 | ||||||
| chr12:21863581
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2238-527T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863581 | ||||||
| chr12:21863707
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2238-653T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863707 | ||||||
| chr12:21863813
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2237+626C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863813 | ||||||
| chr12:21863903
|
A | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2237+536T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863903 | ||||||
| chr12:21863925
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2237+514T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21863925 | ||||||
| chr12:21864013
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2237+426T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21864013 | ||||||
| chr12:21864110
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2237+329G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21864110 | ||||||
| chr12:21864223
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2237+216C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21864223 | ||||||
| chr12:21864394
|
A | T | 1 | a0001c0001t0014g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2237+45T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 19/39 | chr12 | 21864394 | ||||||
| chr12:21864924
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2199-447T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21864924 | ||||||
| chr12:21864932
|
C | T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2199-455G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21864932 | ||||||
| chr12:21865218
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0205others(2): Show | 5 | HG01993.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199-741T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865218 | ||||||
| chr12:21865230
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2199-753A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865230 | ||||||
| chr12:21865251
|
G | T | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2199-774C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865251 | ||||||
| chr12:21865282
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0047 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2199-805T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865282 | ||||||
| chr12:21865483
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2199-1006C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865483 | ||||||
| chr12:21865746
|
G | T | 4 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199-1269C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865746 | ||||||
| chr12:21865814
|
C | T | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2199-1337G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865814 | ||||||
| chr12:21865963
|
CAAA | C | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2199-1489_2199-148 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865963 | ||||||
| chr12:21865964
|
A | G | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2199-1487T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865964 | ||||||
| chr12:21865967
|
G | C | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2199-1490C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21865967 | ||||||
| chr12:21866058
|
G | GA | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 58 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.2199-1582dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866058 | ||||||
| chr12:21866184
|
T | C | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2199-1707A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866184 | ||||||
| chr12:21866224
|
CAT | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0044others(66): Show | 70 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2199-1749_2199-174 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866224 | ||||||
| chr12:21866354
|
TAGAGGGA others(20): Show |
T | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2199-1904_2199-187 others(31): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866354 | ||||||
| chr12:21866459
|
C | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2199-1982G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866459 | ||||||
| chr12:21866669
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0053 | 3 | HG01346.hp2 HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2199-2192G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21866669 | ||||||
| chr12:21867132
|
A | G | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2199-2655T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867132 | ||||||
| chr12:21867149
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2199-2672A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867149 | ||||||
| chr12:21867239
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2199-2762A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867239 | ||||||
| chr12:21867268
|
A | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2199-2791T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867268 | ||||||
| chr12:21867345
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2199-2868A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867345 | ||||||
| chr12:21867453
|
T | C | 1 | a0001c0001t0005g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2199-2976A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867453 | ||||||
| chr12:21867485
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2199-3008C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867485 | ||||||
| chr12:21867575
|
T | C | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2199-3098A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867575 | ||||||
| chr12:21867586
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2199-3109C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867586 | ||||||
| chr12:21867822
|
G | GA | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2199-3346dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21867822 | ||||||
| chr12:21868044
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2199-3567T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868044 | ||||||
| chr12:21868127
|
T | C | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2199-3650A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868127 | ||||||
| chr12:21868261
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2199-3784C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868261 | ||||||
| chr12:21868362
|
G | A | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2199-3885C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868362 | ||||||
| chr12:21868405
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2199-3928G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868405 | ||||||
| chr12:21868406
|
G | A | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2199-3929C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868406 | ||||||
| chr12:21868414
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0083 | 3 | HG02258.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2199-3937G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868414 | ||||||
| chr12:21868435
|
C | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2199-3958G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868435 | ||||||
| chr12:21868455
|
C | T | 5 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(2): Show | 5 | HG02572.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199-3978G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868455 | ||||||
| chr12:21868529
|
C | T | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2199-4052G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868529 | ||||||
| chr12:21868621
|
A | G | 4 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2198+4004T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868621 | ||||||
| chr12:21868768
|
C | T | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2198+3857G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868768 | ||||||
| chr12:21868836
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2198+3789A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868836 | ||||||
| chr12:21868878
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0205others(1): Show | 4 | HG02809.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2198+3747T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21868878 | ||||||
| chr12:21869152
|
G | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2198+3473C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869152 | ||||||
| chr12:21869264
|
TCCTGCTG others(4): Show |
T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2198+3350_2198+336 others(15): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869264 | ||||||
| chr12:21869347
|
C | T | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2198+3278G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869347 | ||||||
| chr12:21869351
|
T | C | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2198+3274A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869351 | ||||||
| chr12:21869441
|
A | G | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2198+3184T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869441 | ||||||
| chr12:21869570
|
C | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2198+3055G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869570 | ||||||
| chr12:21869765
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2198+2860T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869765 | ||||||
| chr12:21869804
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2198+2821A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869804 | ||||||
| chr12:21869946
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2198+2679A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21869946 | ||||||
| chr12:21870091
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2198+2534T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870091 | ||||||
| chr12:21870109
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2198+2516A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870109 | ||||||
| chr12:21870203
|
G | T | 1 | a0001c0004t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2198+2422C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870203 | ||||||
| chr12:21870262
|
T | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2198+2363A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870262 | ||||||
| chr12:21870478
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2198+2147C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870478 | ||||||
| chr12:21870479
|
AACTGCTG others(12): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2198+2127_2198+214 others(23): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870479 | ||||||
| chr12:21870570
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2198+2055G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870570 | ||||||
| chr12:21870625
|
C | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2198+2000G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870625 | ||||||
| chr12:21870747
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2198+1878G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870747 | ||||||
| chr12:21870779
|
TCTA | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(33): Show | 37 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.2198+1843_2198+184 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870779 | ||||||
| chr12:21870803
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2198+1822G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870803 | ||||||
| chr12:21870982
|
G | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00408.hp1 HG01993.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.2198+1643C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21870982 | ||||||
| chr12:21871159
|
T | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2198+1466A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871159 | ||||||
| chr12:21871208
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2198+1417T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871208 | ||||||
| chr12:21871512
|
G | A | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2198+1113C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871512 | ||||||
| chr12:21871775
|
A | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2198+850T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871775 | ||||||
| chr12:21871792
|
C | G | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2198+833G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871792 | ||||||
| chr12:21871805
|
A | C | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2198+820T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871805 | ||||||
| chr12:21871844
|
G | T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2198+781C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871844 | ||||||
| chr12:21871864
|
T | C | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2198+761A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871864 | ||||||
| chr12:21871877
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2198+748A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871877 | ||||||
| chr12:21871914
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0166a0001c0001t0001g0198others(1): Show | 4 | HG02976.hp1 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2198+711G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21871914 | ||||||
| chr12:21872121
|
A | G | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2198+504T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21872121 | ||||||
| chr12:21872122
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2198+503C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21872122 | ||||||
| chr12:21872345
|
T | G | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2198+280A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21872345 | ||||||
| chr12:21872407
|
T | C | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2198+218A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21872407 | ||||||
| chr12:21872432
|
C | A | 2 | a0001c0006t0001g0191a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2198+193G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 18/39 | chr12 | 21872432 | ||||||
| chr12:21872766
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0009t0001g0101 | 3 | NA18959.hp2 NA19065.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2093-36C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21872766 | ||||||
| chr12:21872905
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2093-175T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21872905 | ||||||
| chr12:21872968
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2093-238T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21872968 | ||||||
| chr12:21873292
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 22 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.2093-562A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873292 | ||||||
| chr12:21873443
|
T | C | 1 | a0001c0001t0013g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2093-713A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873443 | ||||||
| chr12:21873453
|
G | T | 4 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093-723C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873453 | ||||||
| chr12:21873490
|
C | A | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2093-760G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873490 | ||||||
| chr12:21873496
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2093-766C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873496 | ||||||
| chr12:21873707
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2093-977T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873707 | ||||||
| chr12:21873896
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2093-1166T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873896 | ||||||
| chr12:21873939
|
T | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2093-1209A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21873939 | ||||||
| chr12:21874071
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2093-1341G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874071 | ||||||
| chr12:21874137
|
C | CA | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2093-1408dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874137 | ||||||
| chr12:21874248
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0003g0141others(1): Show | 4 | HG00140.hp2 HG01496.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092+1406A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874248 | ||||||
| chr12:21874305
|
C | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.2092+1349G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874305 | ||||||
| chr12:21874306
|
T | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.2092+1348A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874306 | ||||||
| chr12:21874508
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2092+1146C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874508 | ||||||
| chr12:21874515
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0041 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2092+1139A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874515 | ||||||
| chr12:21874522
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2092+1132C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874522 | ||||||
| chr12:21874868
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2092+786C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874868 | ||||||
| chr12:21874985
|
T | A | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2092+669A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874985 | ||||||
| chr12:21874990
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2092+664T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21874990 | ||||||
| chr12:21875074
|
AAAAAT | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2092+575_2092+579d others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21875074 | ||||||
| chr12:21875230
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2092+424G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21875230 | ||||||
| chr12:21875321
|
G | A | 5 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(2): Show | 5 | HG02572.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2092+333C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 17/39 | chr12 | 21875321 | ||||||
| chr12:21875966
|
C | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2020-240G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21875966 | ||||||
| chr12:21876033
|
C | T | 2 | a0001c0002t0001g0184a0001c0002t0004g0183 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2020-307G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21876033 | ||||||
| chr12:21876159
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2020-433C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21876159 | ||||||
| chr12:21876194
|
G | A | 4 | a0001c0001t0004g0023a0001c0001t0004g0127a0001c0002t0023g0182others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020-468C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21876194 | ||||||
| chr12:21876749
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2020-1023T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21876749 | ||||||
| chr12:21877052
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2020-1326C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877052 | ||||||
| chr12:21877124
|
G | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2020-1398C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877124 | ||||||
| chr12:21877231
|
C | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2020-1505G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877231 | ||||||
| chr12:21877244
|
A | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0044others(59): Show | 63 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2020-1518T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877244 | ||||||
| chr12:21877628
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0006g0027a0001c0001t0006g0210 | 3 | HG00639.hp1 HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2020-1902T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877628 | ||||||
| chr12:21877653
|
G | A | 2 | a0001c0001t0011g0068a0001c0001t0011g0120 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2020-1927C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877653 | ||||||
| chr12:21877683
|
G | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG00738.hp1 HG01074.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2020-1957C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877683 | ||||||
| chr12:21877877
|
G | A | 1 | a0001c0001t0010g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2020-2151C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21877877 | ||||||
| chr12:21878011
|
TA | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2020-2286delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878011 | ||||||
| chr12:21878071
|
G | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2020-2345C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878071 | ||||||
| chr12:21878223
|
G | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2020-2497C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878223 | ||||||
| chr12:21878256
|
T | C | 1 | a0001c0010t0001g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2020-2530A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878256 | ||||||
| chr12:21878352
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2020-2626C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878352 | ||||||
| chr12:21878382
|
T | C | 3 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183 | 3 | HG02055.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2020-2656A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878382 | ||||||
| chr12:21878739
|
AG | A | 2 | a0001c0001t0001g0080a0001c0001t0002g0078 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2020-3014delC | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878739 | ||||||
| chr12:21878765
|
GT | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(35): Show | 39 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.2020-3040delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878765 | ||||||
| chr12:21878800
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2020-3074A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878800 | ||||||
| chr12:21878953
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2020-3227C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878953 | ||||||
| chr12:21878956
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2020-3230T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21878956 | ||||||
| chr12:21879022
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2020-3296G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879022 | ||||||
| chr12:21879057
|
C | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2020-3331G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879057 | ||||||
| chr12:21879258
|
G | A | 1 | a0001c0001t0018g0003 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2019+3508C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879258 | ||||||
| chr12:21879272
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(35): Show | 39 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.2019+3494C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879272 | ||||||
| chr12:21879358
|
A | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0044others(59): Show | 63 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2019+3408T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879358 | ||||||
| chr12:21879382
|
T | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0065others(2): Show | 5 | HG00408.hp1 HG02129.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2019+3384A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879382 | ||||||
| chr12:21879412
|
C | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 18 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2019+3354G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879412 | ||||||
| chr12:21879568
|
G | C | 1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2019+3198C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879568 | ||||||
| chr12:21879598
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2019+3168T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879598 | ||||||
| chr12:21879608
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(17): Show | 20 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2019+3158G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879608 | ||||||
| chr12:21879637
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2019+3129T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879637 | ||||||
| chr12:21879853
|
G | GA | 8 | a0001c0001t0001g0069a0001c0001t0002g0043a0001c0001t0004g0023others(5): Show | 8 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2019+2912dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879853 | ||||||
| chr12:21879996
|
G | A | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2019+2770C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21879996 | ||||||
| chr12:21880059
|
G | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 18 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2019+2707C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880059 | ||||||
| chr12:21880224
|
T | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2019+2542A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880224 | ||||||
| chr12:21880398
|
C | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG02055.hp1 HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2019+2368G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880398 | ||||||
| chr12:21880426
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0093 | 2 | NA18747.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2019+2340T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880426 | ||||||
| chr12:21880568
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0053 | 3 | HG01346.hp2 HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2019+2198T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880568 | ||||||
| chr12:21880577
|
C | A | 4 | a0001c0001t0001g0069a0001c0001t0002g0043a0001c0001t0004g0127others(1): Show | 4 | HG02572.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2019+2189G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880577 | ||||||
| chr12:21880844
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2019+1922G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21880844 | ||||||
| chr12:21881239
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG00408.hp1 HG02027.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.2019+1527C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881239 | ||||||
| chr12:21881567
|
T | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01168.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+1199A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881567 | ||||||
| chr12:21881686
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0044others(59): Show | 63 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2019+1080G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881686 | ||||||
| chr12:21881707
|
A | AAC | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2019+1057_2019+105 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881707 | ||||||
| chr12:21881707
|
A | AACAC | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2019+1055_2019+105 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881707 | ||||||
| chr12:21881707
|
A | AACACAC | 3 | a0001c0001t0001g0132a0001c0001t0001g0159a0001c0001t0014g0071 | 3 | HG01168.hp1 HG01175.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2019+1053_2019+105 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881707 | ||||||
| chr12:21881752
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2019+1014T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881752 | ||||||
| chr12:21881771
|
C | T | 15 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 15 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2019+995G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881771 | ||||||
| chr12:21881782
|
A | G | 2 | a0001c0001t0004g0023a0001c0002t0023g0182 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2019+984T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881782 | ||||||
| chr12:21881906
|
C | A | 4 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183others(1): Show | 4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+860G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21881906 | ||||||
| chr12:21882004
|
T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2019+762A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882004 | ||||||
| chr12:21882183
|
A | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2019+583T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882183 | ||||||
| chr12:21882273
|
G | C | 1 | a0002c0007t0001g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2019+493C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882273 | ||||||
| chr12:21882313
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2019+453T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882313 | ||||||
| chr12:21882491
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0044others(60): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.2019+275T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882491 | ||||||
| chr12:21882681
|
A | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(2): Show | 5 | HG00621.hp1 NA18959.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.2019+85T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 16/39 | chr12 | 21882681 | ||||||
| chr12:21882939
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1912-66G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21882939 | ||||||
| chr12:21882949
|
T | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1912-76A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21882949 | ||||||
| chr12:21883107
|
A | G | 6 | a0001c0001t0001g0069a0001c0001t0002g0043a0001c0001t0004g0127others(3): Show | 6 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-234T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883107 | ||||||
| chr12:21883152
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1912-279A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883152 | ||||||
| chr12:21883259
|
C | T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1912-386G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883259 | ||||||
| chr12:21883293
|
A | C | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1912-420T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883293 | ||||||
| chr12:21883300
|
G | A | 1 | a0001c0001t0015g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1912-427C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883300 | ||||||
| chr12:21883412
|
A | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0171 | 2 | NA18978.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1912-539T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883412 | ||||||
| chr12:21883725
|
A | ATT | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1912-854_1912-853d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883725 | ||||||
| chr12:21883737
|
C | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1912-864G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21883737 | ||||||
| chr12:21884045
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1912-1172A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884045 | ||||||
| chr12:21884075
|
CTT | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1912-1204_1912-120 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884075 | ||||||
| chr12:21884168
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1912-1295A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884168 | ||||||
| chr12:21884269
|
T | A | 1 | a0001c0001t0008g0189 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1912-1396A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884269 | ||||||
| chr12:21884284
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1912-1411C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884284 | ||||||
| chr12:21884327
|
C | T | 1 | a0001c0001t0014g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1912-1454G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884327 | ||||||
| chr12:21884333
|
G | A | 23 | a0001c0001t0001g0050a0001c0001t0001g0130a0001c0001t0001g0131others(20): Show | 23 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1912-1460C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884333 | ||||||
| chr12:21884415
|
G | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1912-1542C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884415 | ||||||
| chr12:21884439
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1912-1566A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884439 | ||||||
| chr12:21884673
|
G | T | 1 | a0001c0005t0001g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1912-1800C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884673 | ||||||
| chr12:21884782
|
T | TAAAGAG | 167 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1912-1910_1912-190 others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884782 | ||||||
| chr12:21884782
|
T | TAG | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1912-1911_1912-191 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21884782 | ||||||
| chr12:21885101
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1912-2228C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885101 | ||||||
| chr12:21885329
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1912-2456C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885329 | ||||||
| chr12:21885361
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1911+2465A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885361 | ||||||
| chr12:21885417
|
T | A | 4 | a0001c0001t0002g0043a0001c0006t0001g0042a0001c0006t0001g0191others(1): Show | 4 | HG02647.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1911+2409A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885417 | ||||||
| chr12:21885545
|
T | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 96 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1911+2281A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885545 | ||||||
| chr12:21885784
|
A | G | 1 | a0001c0001t0021g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1911+2042T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885784 | ||||||
| chr12:21885964
|
G | T | 3 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183 | 3 | HG02055.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1911+1862C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21885964 | ||||||
| chr12:21886246
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0050others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1911+1580C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21886246 | ||||||
| chr12:21886320
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0050others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1911+1506A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21886320 | ||||||
| chr12:21886405
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1911+1421C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21886405 | ||||||
| chr12:21886645
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1911+1181T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21886645 | ||||||
| chr12:21886651
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1911+1175G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21886651 | ||||||
| chr12:21887053
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(41): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1911+773G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887053 | ||||||
| chr12:21887107
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1911+719C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887107 | ||||||
| chr12:21887113
|
G | GC | 23 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0072others(20): Show | 23 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1911+712dupG | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887113 | ||||||
| chr12:21887390
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1911+436C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887390 | ||||||
| chr12:21887552
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1911+274T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887552 | ||||||
| chr12:21887574
|
C | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0047 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1911+252G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 15/39 | chr12 | 21887574 | ||||||
| chr12:21888110
|
GGACAGAG others(5): Show |
G | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1803-188_1803-177d others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888110 | ||||||
| chr12:21888216
|
T | C | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183others(3): Show | 6 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803-282A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888216 | ||||||
| chr12:21888336
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0160 | 2 | HG02132.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1803-402C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888336 | ||||||
| chr12:21888752
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1803-818C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888752 | ||||||
| chr12:21888921
|
TA | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1803-988delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888921 | ||||||
| chr12:21888985
|
T | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(99): Show | 102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1803-1051A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21888985 | ||||||
| chr12:21889219
|
G | T | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1803-1285C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889219 | ||||||
| chr12:21889314
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0102 | 2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1803-1380T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889314 | ||||||
| chr12:21889341
|
CATT | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-1410_1803-140 others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889341 | ||||||
| chr12:21889444
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1803-1510C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889444 | ||||||
| chr12:21889476
|
C | T | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183others(3): Show | 6 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803-1542G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889476 | ||||||
| chr12:21889562
|
G | C | 8 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0174others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1803-1628C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889562 | ||||||
| chr12:21889578
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1803-1644C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889578 | ||||||
| chr12:21889613
|
T | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1803-1679A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889613 | ||||||
| chr12:21889626
|
C | A | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1803-1692G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889626 | ||||||
| chr12:21889687
|
G | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(41): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1803-1753C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889687 | ||||||
| chr12:21889743
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0053 | 3 | HG01346.hp2 HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1803-1809A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889743 | ||||||
| chr12:21889806
|
A | G | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 96 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1803-1872T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21889806 | ||||||
| chr12:21890307
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1803-2373G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890307 | ||||||
| chr12:21890371
|
C | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1803-2437G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890371 | ||||||
| chr12:21890737
|
G | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1803-2803C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890737 | ||||||
| chr12:21890935
|
C | T | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1803-3001G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890935 | ||||||
| chr12:21890983
|
TA | T | 8 | a0001c0001t0001g0081a0001c0001t0001g0116a0001c0002t0001g0184others(5): Show | 8 | HG02055.hp2 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1802+3048delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890983 | ||||||
| chr12:21890984
|
A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 72 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1802+3048T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890984 | ||||||
| chr12:21890985
|
A | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02809.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1802+3047T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890985 | ||||||
| chr12:21890986
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1802+3046T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890986 | ||||||
| chr12:21890993
|
A | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 21 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1802+3039T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21890993 | ||||||
| chr12:21891274
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1802+2758C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891274 | ||||||
| chr12:21891276
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1802+2756G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891276 | ||||||
| chr12:21891373
|
ATAGT | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0075others(14): Show | 17 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1802+2655_1802+265 others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891373 | ||||||
| chr12:21891410
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0021others(45): Show | 48 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1802+2622G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891410 | ||||||
| chr12:21891658
|
A | G | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1802+2374T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891658 | ||||||
| chr12:21891791
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1802+2241T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891791 | ||||||
| chr12:21891873
|
C | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1802+2159G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891873 | ||||||
| chr12:21891909
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1802+2123G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21891909 | ||||||
| chr12:21892220
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1802+1812C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892220 | ||||||
| chr12:21892245
|
GACACC | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0053 | 3 | HG01346.hp2 HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1802+1782_1802+178 others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892245 | ||||||
| chr12:21892730
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0083 | 3 | HG02258.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1802+1302T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892730 | ||||||
| chr12:21892837
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0032others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1802+1195A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892837 | ||||||
| chr12:21892865
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1802+1167G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892865 | ||||||
| chr12:21892919
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1802+1113T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21892919 | ||||||
| chr12:21893124
|
G | A | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1802+908C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893124 | ||||||
| chr12:21893143
|
A | G | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183others(3): Show | 6 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1802+889T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893143 | ||||||
| chr12:21893183
|
A | G | 3 | a0001c0001t0002g0043a0001c0006t0001g0191a0001c0006t0005g0192 | 3 | HG02647.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1802+849T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893183 | ||||||
| chr12:21893194
|
T | TATC | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1802+837_1802+838i others(5): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893194 | ||||||
| chr12:21893204
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1802+828G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893204 | ||||||
| chr12:21893309
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1802+723A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893309 | ||||||
| chr12:21893320
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1802+712T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893320 | ||||||
| chr12:21893573
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1802+459A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893573 | ||||||
| chr12:21893586
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1802+446T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893586 | ||||||
| chr12:21893834
|
A | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1802+198T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893834 | ||||||
| chr12:21893858
|
T | G | 1 | a0001c0001t0002g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1802+174A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 14/39 | chr12 | 21893858 | ||||||
| chr12:21894217
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1660-43C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894217 | ||||||
| chr12:21894240
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1660-66G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894240 | ||||||
| chr12:21894407
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1660-233G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894407 | ||||||
| chr12:21894414
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1660-240C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894414 | ||||||
| chr12:21894450
|
G | T | 3 | a0001c0001t0002g0043a0001c0006t0001g0191a0001c0006t0005g0192 | 3 | HG02647.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1660-276C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894450 | ||||||
| chr12:21894521
|
C | T | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1660-347G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894521 | ||||||
| chr12:21894539
|
TCTGTTGT others(95): Show |
T | 70 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0032others(67): Show | 71 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1660-467_1660-366d others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894539 | ||||||
| chr12:21894614
|
AT | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1660-441delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894614 | ||||||
| chr12:21894671
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1660-497C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894671 | ||||||
| chr12:21894774
|
C | G | 19 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(16): Show | 19 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1659+501G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894774 | ||||||
| chr12:21894802
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1659+473A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21894802 | ||||||
| chr12:21895235
|
G | A | 1 | a0001c0001t0004g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1659+40C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 13/39 | chr12 | 21895235 | ||||||
| chr12:21895444
|
T | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1619-129A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895444 | ||||||
| chr12:21895476
|
C | T | 1 | a0001c0001t0017g0143 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1619-161G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895476 | ||||||
| chr12:21895629
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1619-314A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895629 | ||||||
| chr12:21895649
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0083 | 3 | HG02258.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1619-334C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895649 | ||||||
| chr12:21895710
|
A | AT | 2 | a0001c0001t0001g0044a0001c0001t0001g0047 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1619-396dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895710 | ||||||
| chr12:21895859
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1619-544G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21895859 | ||||||
| chr12:21896079
|
C | CT | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00408.hp1 HG02027.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1619-765dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896079 | ||||||
| chr12:21896079
|
CT | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(19): Show | 22 | HG01168.hp2 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1619-765delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896079 | ||||||
| chr12:21896092
|
TTTTTTTA others(1): Show |
T | 6 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0130others(3): Show | 6 | HG00323.hp1 HG00438.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-785_1619-778d others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896092 | ||||||
| chr12:21896093
|
TTTTTTAC | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1619-785_1619-779d others(9): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896093 | ||||||
| chr12:21896104
|
T | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1619-789A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896104 | ||||||
| chr12:21896390
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1619-1075T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896390 | ||||||
| chr12:21896640
|
C | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1619-1325G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896640 | ||||||
| chr12:21896654
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1619-1339T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896654 | ||||||
| chr12:21896985
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1619-1670C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21896985 | ||||||
| chr12:21897045
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1619-1730T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897045 | ||||||
| chr12:21897122
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1619-1807G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897122 | ||||||
| chr12:21897272
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1619-1957A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897272 | ||||||
| chr12:21897691
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-2376C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897691 | ||||||
| chr12:21897863
|
C | CA | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1619-2549dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897863 | ||||||
| chr12:21897976
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG02027.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1619-2661T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21897976 | ||||||
| chr12:21898155
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1619-2840G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898155 | ||||||
| chr12:21898362
|
T | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(50): Show | 53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1619-3047A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898362 | ||||||
| chr12:21898533
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1619-3218C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898533 | ||||||
| chr12:21898625
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1619-3310A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898625 | ||||||
| chr12:21898765
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1619-3450T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898765 | ||||||
| chr12:21898880
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-3565C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898880 | ||||||
| chr12:21898906
|
G | A | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1619-3591C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21898906 | ||||||
| chr12:21899213
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1619-3898C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899213 | ||||||
| chr12:21899448
|
T | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1619-4133A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899448 | ||||||
| chr12:21899507
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1619-4192G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899507 | ||||||
| chr12:21899631
|
C | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1619-4316G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899631 | ||||||
| chr12:21899667
|
C | T | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1619-4352G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899667 | ||||||
| chr12:21899668
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1619-4353T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899668 | ||||||
| chr12:21899751
|
C | T | 1 | a0001c0001t0003g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1619-4436G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899751 | ||||||
| chr12:21899810
|
G | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1619-4495C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21899810 | ||||||
| chr12:21900107
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1619-4792C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900107 | ||||||
| chr12:21900124
|
G | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1619-4809C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900124 | ||||||
| chr12:21900204
|
G | A | 1 | a0001c0002t0012g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-4889C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900204 | ||||||
| chr12:21900351
|
G | T | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619-5036C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900351 | ||||||
| chr12:21900354
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1619-5039C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900354 | ||||||
| chr12:21900423
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1619-5108C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900423 | ||||||
| chr12:21900540
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1619-5225C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900540 | ||||||
| chr12:21900658
|
C | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1619-5343G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900658 | ||||||
| chr12:21900835
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1618+5291T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900835 | ||||||
| chr12:21900919
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1618+5207C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21900919 | ||||||
| chr12:21901001
|
G | A | 2 | a0001c0001t0001g0174a0001c0003t0016g0173 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1618+5125C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901001 | ||||||
| chr12:21901044
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1618+5082G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901044 | ||||||
| chr12:21901095
|
CAG | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1618+5029_1618+503 others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901095 | ||||||
| chr12:21901446
|
A | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1618+4680T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901446 | ||||||
| chr12:21901641
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0006g0142 | 3 | HG00738.hp1 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1618+4485G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901641 | ||||||
| chr12:21901782
|
A | G | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1618+4344T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901782 | ||||||
| chr12:21901918
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1618+4208T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21901918 | ||||||
| chr12:21902070
|
A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1618+4056T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902070 | ||||||
| chr12:21902075
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1618+4051T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902075 | ||||||
| chr12:21902093
|
C | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1618+4033G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902093 | ||||||
| chr12:21902155
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0006g0142 | 3 | HG00738.hp1 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1618+3971C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902155 | ||||||
| chr12:21902180
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1618+3946G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902180 | ||||||
| chr12:21902249
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1618+3877G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902249 | ||||||
| chr12:21902495
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1618+3631T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902495 | ||||||
| chr12:21902694
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1618+3432C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902694 | ||||||
| chr12:21902906
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1618+3220A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902906 | ||||||
| chr12:21902916
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0193 | 3 | HG01106.hp1 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1618+3210C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902916 | ||||||
| chr12:21902987
|
C | A | 7 | a0001c0001t0001g0053a0001c0001t0002g0043a0001c0002t0001g0184others(4): Show | 7 | HG02055.hp2 HG02735.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+3139G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21902987 | ||||||
| chr12:21903123
|
C | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1618+3003G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903123 | ||||||
| chr12:21903328
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1618+2798C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903328 | ||||||
| chr12:21903622
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1618+2504G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903622 | ||||||
| chr12:21903664
|
T | G | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1618+2462A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903664 | ||||||
| chr12:21903768
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1618+2358T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903768 | ||||||
| chr12:21903796
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1618+2330C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903796 | ||||||
| chr12:21903883
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1618+2243G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903883 | ||||||
| chr12:21903903
|
C | T | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1618+2223G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903903 | ||||||
| chr12:21903920
|
A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1618+2206T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21903920 | ||||||
| chr12:21904094
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1618+2032C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904094 | ||||||
| chr12:21904136
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0203others(1): Show | 4 | HG02630.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+1990G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904136 | ||||||
| chr12:21904165
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1618+1961T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904165 | ||||||
| chr12:21904180
|
A | AT | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1618+1945_1618+194 others(5): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904180 | ||||||
| chr12:21904187
|
C | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0029others(34): Show | 37 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1618+1939G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904187 | ||||||
| chr12:21904382
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1618+1744T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904382 | ||||||
| chr12:21904459
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1618+1667A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904459 | ||||||
| chr12:21904465
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1618+1661T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904465 | ||||||
| chr12:21904534
|
C | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG01074.hp2 HG01168.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+1592G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904534 | ||||||
| chr12:21904693
|
G | T | 3 | a0001c0006t0001g0042a0001c0006t0001g0191a0001c0006t0005g0192 | 3 | HG02647.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1618+1433C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904693 | ||||||
| chr12:21904979
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1618+1147G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904979 | ||||||
| chr12:21904980
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1618+1146T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21904980 | ||||||
| chr12:21905230
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1618+896A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905230 | ||||||
| chr12:21905240
|
C | T | 1 | a0001c0001t0020g0140 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1618+886G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905240 | ||||||
| chr12:21905251
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1618+875G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905251 | ||||||
| chr12:21905263
|
G | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1618+863C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905263 | ||||||
| chr12:21905351
|
C | CAT | 6 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0089others(3): Show | 6 | HG00639.hp1 HG01433.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618+773_1618+774d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905351 | ||||||
| chr12:21905351
|
C | CATAT | 11 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(8): Show | 11 | HG00438.hp2 HG00558.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1618+771_1618+774d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905351 | ||||||
| chr12:21905353
|
T | C | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1618+773A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905353 | ||||||
| chr12:21905410
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1618+716A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905410 | ||||||
| chr12:21905423
|
A | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1618+703T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905423 | ||||||
| chr12:21905475
|
A | G | 2 | a0001c0006t0001g0191a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1618+651T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905475 | ||||||
| chr12:21905549
|
C | T | 3 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183 | 3 | HG02055.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1618+577G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905549 | ||||||
| chr12:21905588
|
A | G | 1 | a0001c0004t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1618+538T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905588 | ||||||
| chr12:21905944
|
T | C | 1 | a0001c0001t0021g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1618+182A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 12/39 | chr12 | 21905944 | ||||||
| chr12:21906437
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1456-149T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21906437 | ||||||
| chr12:21906485
|
C | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1456-197G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21906485 | ||||||
| chr12:21906683
|
C | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1456-395G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21906683 | ||||||
| chr12:21906704
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1456-416T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21906704 | ||||||
| chr12:21906927
|
C | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1456-639G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21906927 | ||||||
| chr12:21907089
|
A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1456-801T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21907089 | ||||||
| chr12:21907314
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1455+763T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21907314 | ||||||
| chr12:21907734
|
T | G | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1455+343A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21907734 | ||||||
| chr12:21907775
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1455+302C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21907775 | ||||||
| chr12:21907922
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1455+155A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 11/39 | chr12 | 21907922 | ||||||
| chr12:21908322
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1321-111A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908322 | ||||||
| chr12:21908498
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1321-287A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908498 | ||||||
| chr12:21908538
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1321-327G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908538 | ||||||
| chr12:21908753
|
A | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01168.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-542T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908753 | ||||||
| chr12:21908797
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1321-586T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908797 | ||||||
| chr12:21908806
|
T | A | 1 | a0001c0001t0001g0005 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1321-595A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908806 | ||||||
| chr12:21908820
|
T | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1321-609A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21908820 | ||||||
| chr12:21909387
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1320+770C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21909387 | ||||||
| chr12:21909414
|
A | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1320+743T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21909414 | ||||||
| chr12:21909681
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1320+476T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21909681 | ||||||
| chr12:21909964
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1320+193T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 10/39 | chr12 | 21909964 | ||||||
| chr12:21910317
|
CA | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(72): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
splice_region_variant&intron_variant | LOW | c.1165-6delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910317 | ||||||
| chr12:21910366
|
A | G | 3 | a0001c0006t0001g0042a0001c0006t0001g0191a0001c0006t0005g0192 | 3 | HG02647.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1165-54T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910366 | ||||||
| chr12:21910403
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1165-91T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910403 | ||||||
| chr12:21910404
|
T | C | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1165-92A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910404 | ||||||
| chr12:21910419
|
A | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1165-107T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910419 | ||||||
| chr12:21910741
|
A | T | 12 | a0001c0001t0001g0050a0001c0001t0001g0131a0001c0001t0001g0200others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164+85T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910741 | ||||||
| chr12:21910803
|
T | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1164+23A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910803 | ||||||
| chr12:21910815
|
C | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1164+11G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 9/39 | chr12 | 21910815 | ||||||
| chr12:21911037
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1012-59T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911037 | ||||||
| chr12:21911254
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1012-276A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911254 | ||||||
| chr12:21911283
|
G | C | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1012-305C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911283 | ||||||
| chr12:21911326
|
T | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1012-348A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911326 | ||||||
| chr12:21911459
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1012-481C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911459 | ||||||
| chr12:21911639
|
T | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1012-661A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911639 | ||||||
| chr12:21911780
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(43): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1012-802T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911780 | ||||||
| chr12:21911828
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1012-850C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911828 | ||||||
| chr12:21911895
|
A | ATTTCCAT others(6): Show |
208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1012-918_1012-917i others(15): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911895 | ||||||
| chr12:21911935
|
G | C | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1011+937C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21911935 | ||||||
| chr12:21912215
|
C | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1011+657G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912215 | ||||||
| chr12:21912239
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1011+633T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912239 | ||||||
| chr12:21912316
|
T | C | 1 | a0001c0005t0001g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1011+556A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912316 | ||||||
| chr12:21912336
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1011+536G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912336 | ||||||
| chr12:21912422
|
CAG | C | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1011+448_1011+449d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912422 | ||||||
| chr12:21912529
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1011+343T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912529 | ||||||
| chr12:21912740
|
T | G | 1 | a0001c0001t0001g0009 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1011+132A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912740 | ||||||
| chr12:21912765
|
G | GA | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1011+106dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912765 | ||||||
| chr12:21912765
|
G | GAA | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(84): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1011+105_1011+106d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 8/39 | chr12 | 21912765 | ||||||
| chr12:21913083
|
G | GA | 8 | a0001c0001t0001g0040a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00408.hp2 HG02129.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-18dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21913083 | ||||||
| chr12:21913246
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-180G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21913246 | ||||||
| chr12:21913353
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.817-287T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21913353 | ||||||
| chr12:21913624
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.817-558A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21913624 | ||||||
| chr12:21913973
|
A | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0205others(1): Show | 4 | HG02809.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-907T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21913973 | ||||||
| chr12:21914159
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.817-1093A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914159 | ||||||
| chr12:21914235
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.817-1169C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914235 | ||||||
| chr12:21914274
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.817-1208A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914274 | ||||||
| chr12:21914283
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.817-1217A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914283 | ||||||
| chr12:21914551
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.816+1117G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914551 | ||||||
| chr12:21914661
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.816+1007C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914661 | ||||||
| chr12:21914900
|
CT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.816+767delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21914900 | ||||||
| chr12:21915027
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.816+641T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915027 | ||||||
| chr12:21915152
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.816+516G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915152 | ||||||
| chr12:21915215
|
T | TTA | 9 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG00438.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.816+451_816+452dup others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915215 | ||||||
| chr12:21915215
|
TTA | T | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.816+451_816+452del others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915215 | ||||||
| chr12:21915225
|
A | ATG | 12 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG00280.hp1 HG02040.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+441_816+442dup others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915225
|
A | ATGTGTG | 8 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0005g0067others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+437_816+442dup others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915225
|
A | G | 3 | a0001c0003t0009g0209a0002c0007t0001g0039a0002c0007t0001g0049 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.816+443T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915225
|
ATG | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0065others(7): Show | 10 | HG02040.hp2 HG02129.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+441_816+442del others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915225
|
ATGTG | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0097others(1): Show | 4 | HG01346.hp1 HG01516.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+439_816+442del others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915225
|
ATGTGTGT others(1): Show |
A | 27 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0026others(24): Show | 27 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.816+435_816+442del others(8): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915225 | ||||||
| chr12:21915227
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(54): Show | 58 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.816+441C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915227 | ||||||
| chr12:21915229
|
G | A | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.816+439C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915229 | ||||||
| chr12:21915251
|
G | GTGTGTAT others(16): Show |
1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+416_816+417ins others(23): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915251 | ||||||
| chr12:21915251
|
G | GTGTGTGT others(18): Show |
1 | a0001c0001t0014g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+416_816+417ins others(25): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915251 | ||||||
| chr12:21915259
|
G | A | 2 | a0001c0001t0014g0071a0001c0008t0001g0179 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.816+409C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915259 | ||||||
| chr12:21915259
|
G | GTATATAA others(20): Show |
6 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG00408.hp2 HG02129.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+408_816+409ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915259 | ||||||
| chr12:21915263
|
A | G | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 13 | HG01884.hp2 HG02040.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.816+405T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915263 | ||||||
| chr12:21915267
|
A | AC | 8 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139others(5): Show | 8 | HG00408.hp2 HG02129.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+400_816+401ins others(1): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915267 | ||||||
| chr12:21915278
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.816+390T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915278 | ||||||
| chr12:21915286
|
G | GTA | 129 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.816+380_816+381dup others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915286 | ||||||
| chr12:21915286
|
G | GTATGTAT others(25): Show |
66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.816+381_816+382ins others(32): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915286 | ||||||
| chr12:21915338
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.816+330C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915338 | ||||||
| chr12:21915355
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.816+313T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915355 | ||||||
| chr12:21915358
|
ATGTGTAT others(5): Show |
A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.816+298_816+309del others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915358 | ||||||
| chr12:21915376
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.816+292T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915376 | ||||||
| chr12:21915383
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.816+285C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915383 | ||||||
| chr12:21915400
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.816+268T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915400 | ||||||
| chr12:21915411
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.816+257C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915411 | ||||||
| chr12:21915415
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.816+253G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915415 | ||||||
| chr12:21915462
|
A | G | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+206T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915462 | ||||||
| chr12:21915472
|
GTATA | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0132others(25): Show | 28 | HG00280.hp2 HG00438.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.816+192_816+195del others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915472 | ||||||
| chr12:21915472
|
GTATATA | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0040others(40): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.816+190_816+195del others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915472 | ||||||
| chr12:21915474
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0166a0001c0001t0001g0186 | 3 | HG02258.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.816+194T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915474 | ||||||
| chr12:21915476
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0166a0001c0001t0001g0186 | 3 | HG02258.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.816+192T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915476 | ||||||
| chr12:21915478
|
A | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(162): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.816+190T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915478 | ||||||
| chr12:21915492
|
G | A | 11 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG00438.hp2 HG00558.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+176C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915492 | ||||||
| chr12:21915494
|
G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.816+174C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915494 | ||||||
| chr12:21915496
|
G | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(127): Show | 130 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.816+172C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915496 | ||||||
| chr12:21915498
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.816+170C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915498 | ||||||
| chr12:21915500
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.816+168C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915500 | ||||||
| chr12:21915502
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.816+166T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915502 | ||||||
| chr12:21915506
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.816+161_816+162ins others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915506 | ||||||
| chr12:21915506
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0022g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.816+161_816+162ins others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915506 | ||||||
| chr12:21915506
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.816+161_816+162ins others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915506 | ||||||
| chr12:21915506
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0013g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.816+161_816+162ins others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915506 | ||||||
| chr12:21915508
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+159_816+160ins others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915508 | ||||||
| chr12:21915508
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | HG03516.hp2 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+159_816+160ins others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915508 | ||||||
| chr12:21915508
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.816+159_816+160ins others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915508 | ||||||
| chr12:21915508
|
A | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0013g0092others(1): Show | 4 | HG00280.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+160T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915508 | ||||||
| chr12:21915510
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0083 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.816+157_816+158ins others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915510 | ||||||
| chr12:21915510
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0046 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.816+157_816+158ins others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915510 | ||||||
| chr12:21915510
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0058 | 2 | HG02486.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.816+157_816+158ins others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915510 | ||||||
| chr12:21915510
|
A | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0047others(8): Show | 11 | HG00280.hp1 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+158T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915510 | ||||||
| chr12:21915512
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.816+155_816+156ins others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915512 | ||||||
| chr12:21915512
|
A | ATTTTTTT others(4): Show |
6 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0168others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+155_816+156ins others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915512 | ||||||
| chr12:21915512
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0003g0141a0001c0001t0006g0142 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.816+155_816+156ins others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915512 | ||||||
| chr12:21915512
|
A | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00280.hp1 HG01891.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.816+156T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915512 | ||||||
| chr12:21915514
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(31): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01168.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(29): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(17): Show |
1 | a0003c0012t0001g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(24): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0006g0210 | 3 | HG01433.hp1 HG01433.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(17): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(11): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(24): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0001g0080 | 3 | HG02735.hp1 HG02976.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(25): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0089a0001c0002t0001g0184 | 2 | HG02055.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.816+153_816+154ins others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(20): Show |
5 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0082others(2): Show | 5 | HG01884.hp1 HG01934.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(29): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.816+153_816+154ins others(15): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(18): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01255.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(21): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0115a0001c0001t0021g0122 | 3 | HG00140.hp1 HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.816+153_816+154ins others(23): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0004g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(24): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(18): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0072others(2): Show | 5 | HG00639.hp1 HG02293.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(25): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0005g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.816+153_816+154ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(13): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0096others(3): Show | 6 | HG00323.hp1 HG02027.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(14): Show |
7 | a0001c0001t0001g0029a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(21): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(15): Show |
1 | a0001c0004t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(22): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0093a0001c0001t0001g0181 | 3 | HG02257.hp1 NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(23): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(24): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(20): Show |
1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0109others(2): Show | 5 | HG00639.hp2 HG00738.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(19): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(13): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0074others(3): Show | 6 | HG00558.hp1 HG01261.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(14): Show |
14 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0066others(11): Show | 14 | HG00438.hp2 HG01106.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(21): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0063 | 2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(22): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(7): Show |
1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(12): Show |
2 | a0001c0001t0001g0055a0001c0001t0010g0064 | 2 | NA18747.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.816+153_816+154ins others(19): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(13): Show |
7 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0030others(4): Show | 7 | HG01516.hp1 HG03017.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(14): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(3): Show | 6 | HG03486.hp1 NA18947.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+153_816+154ins others(21): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(15): Show |
1 | a0001c0001t0001g0075 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(22): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(19): Show |
1 | a0001c0006t0005g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(26): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATATTT others(20): Show |
1 | a0001c0006t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(27): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATTTTT others(12): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0010g0062 | 3 | HG00408.hp1 HG02132.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.816+153_816+154ins others(19): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATTTTT others(13): Show |
1 | a0001c0001t0001g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.816+153_816+154ins others(20): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATATTTTT others(16): Show |
1 | a0001c0001t0001g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.816+153_816+154ins others(23): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATTTTTTT others(3): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0002g0126others(3): Show | 6 | HG01175.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+144_816+153dup others(10): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0123a0001c0001t0001g0125others(16): Show | 20 | HG01255.hp2 HG01496.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+143_816+153dup others(11): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATTTTTTT others(5): Show |
15 | a0001c0001t0001g0050a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.816+142_816+153dup others(12): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0169a0001c0001t0001g0178 | 3 | HG02055.hp1 HG02300.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.816+141_816+153dup others(13): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | ATTTTTTT others(7): Show |
9 | a0001c0001t0001g0040a0001c0001t0001g0131a0001c0001t0001g0137others(6): Show | 9 | HG00408.hp2 HG02129.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.816+140_816+153dup others(14): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915514
|
A | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.816+154T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 7/39 | chr12 | 21915514 | ||||||
| chr12:21915915
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
splice_region_variant&intron_variant | LOW | c.574-5C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21915915 | ||||||
| chr12:21915933
|
G | A | 1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.574-23C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21915933 | ||||||
| chr12:21916180
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.574-270C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21916180 | ||||||
| chr12:21916451
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.573+486T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21916451 | ||||||
| chr12:21916629
|
A | G | 1 | a0001c0001t0020g0140 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.573+308T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21916629 | ||||||
| chr12:21916750
|
A | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.573+187T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 6/39 | chr12 | 21916750 | ||||||
| chr12:21917168
|
G | A | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.407-65C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917168 | ||||||
| chr12:21917297
|
T | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-194A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917297 | ||||||
| chr12:21917331
|
T | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0008g0188others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-228A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917331 | ||||||
| chr12:21917449
|
C | G | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.407-346G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917449 | ||||||
| chr12:21917510
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.407-407G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917510 | ||||||
| chr12:21917873
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.407-770T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21917873 | ||||||
| chr12:21918030
|
TA | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.407-928delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21918030 | ||||||
| chr12:21918030
|
TAA | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(49): Show | 52 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.407-929_407-928del others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21918030 | ||||||
| chr12:21918139
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.407-1036G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21918139 | ||||||
| chr12:21918861
|
G | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.407-1758C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21918861 | ||||||
| chr12:21919248
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.407-2145T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21919248 | ||||||
| chr12:21919323
|
A | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(49): Show | 52 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.407-2220T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21919323 | ||||||
| chr12:21919382
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.407-2279C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21919382 | ||||||
| chr12:21919405
|
A | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.407-2302T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21919405 | ||||||
| chr12:21919595
|
C | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.407-2492G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21919595 | ||||||
| chr12:21920165
|
C | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.407-3062G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21920165 | ||||||
| chr12:21920320
|
T | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.407-3217A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21920320 | ||||||
| chr12:21920629
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(72): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.407-3526A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21920629 | ||||||
| chr12:21920753
|
C | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.407-3650G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21920753 | ||||||
| chr12:21921200
|
G | T | 3 | a0001c0006t0001g0042a0001c0006t0001g0191a0001c0006t0005g0192 | 3 | HG02647.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.407-4097C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921200 | ||||||
| chr12:21921304
|
G | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.407-4201C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921304 | ||||||
| chr12:21921435
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.407-4332A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921435 | ||||||
| chr12:21921550
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.406+4392G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921550 | ||||||
| chr12:21921682
|
G | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+4260C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921682 | ||||||
| chr12:21921887
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0205others(1): Show | 4 | HG02809.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+4055T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921887 | ||||||
| chr12:21921992
|
G | A | 2 | a0001c0001t0001g0174a0001c0003t0016g0173 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.406+3950C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21921992 | ||||||
| chr12:21922205
|
A | T | 1 | a0001c0006t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.406+3737T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922205 | ||||||
| chr12:21922292
|
A | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.406+3650T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922292 | ||||||
| chr12:21922460
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02129.hp2 NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.406+3482T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922460 | ||||||
| chr12:21922493
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.406+3449T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922493 | ||||||
| chr12:21922739
|
CT | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0164a0001c0002t0012g0002others(2): Show | 5 | HG00438.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+3202delA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922739 | ||||||
| chr12:21922751
|
C | CT | 97 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 97 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.406+3190dupA | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922751 | ||||||
| chr12:21922858
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+3084A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21922858 | ||||||
| chr12:21923016
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.406+2926T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923016 | ||||||
| chr12:21923026
|
T | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.406+2916A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923026 | ||||||
| chr12:21923083
|
GAA | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.406+2857_406+2858d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923083 | ||||||
| chr12:21923090
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+2852T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923090 | ||||||
| chr12:21923176
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+2766T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923176 | ||||||
| chr12:21923195
|
A | G | 2 | a0001c0006t0001g0191a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.406+2747T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923195 | ||||||
| chr12:21923239
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0193 | 3 | HG01106.hp1 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.406+2703C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923239 | ||||||
| chr12:21923522
|
A | C | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.406+2420T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923522 | ||||||
| chr12:21923562
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.406+2380T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21923562 | ||||||
| chr12:21924039
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0072others(14): Show | 17 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.406+1903A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21924039 | ||||||
| chr12:21924253
|
A | G | 1 | a0001c0001t0022g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.406+1689T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21924253 | ||||||
| chr12:21924353
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+1589T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21924353 | ||||||
| chr12:21924457
|
G | A | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.406+1485C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21924457 | ||||||
| chr12:21924477
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+1465C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21924477 | ||||||
| chr12:21925081
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+861T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925081 | ||||||
| chr12:21925139
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.406+803T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925139 | ||||||
| chr12:21925215
|
G | A | 1 | a0001c0001t0013g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.406+727C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925215 | ||||||
| chr12:21925231
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.406+711A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925231 | ||||||
| chr12:21925311
|
G | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.406+631C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925311 | ||||||
| chr12:21925311
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406+631C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925311 | ||||||
| chr12:21925372
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.406+570T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925372 | ||||||
| chr12:21925457
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.406+485T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925457 | ||||||
| chr12:21925622
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.406+320A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925622 | ||||||
| chr12:21925637
|
T | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.406+305A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925637 | ||||||
| chr12:21925688
|
C | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02129.hp2 NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.406+254G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925688 | ||||||
| chr12:21925904
|
T | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.406+38A>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 5/39 | chr12 | 21925904 | ||||||
| chr12:21926079
|
C | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.285-16G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926079 | ||||||
| chr12:21926085
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18988.hp2 NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.285-22G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926085 | ||||||
| chr12:21926159
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-96T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926159 | ||||||
| chr12:21926239
|
C | T | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285-176G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926239 | ||||||
| chr12:21926329
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.285-266A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926329 | ||||||
| chr12:21926384
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.285-321C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926384 | ||||||
| chr12:21926448
|
C | T | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.285-385G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926448 | ||||||
| chr12:21926542
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-479G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926542 | ||||||
| chr12:21926633
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.285-570C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926633 | ||||||
| chr12:21926734
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.285-671T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926734 | ||||||
| chr12:21926792
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-729G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926792 | ||||||
| chr12:21926793
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-730T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21926793 | ||||||
| chr12:21928077
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.285-2014T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928077 | ||||||
| chr12:21928314
|
G | GGGAA | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.285-2255_285-2252d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928314 | ||||||
| chr12:21928337
|
AAGGGAAG others(106): Show |
A | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.285-2387_285-2275d others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928337 | ||||||
| chr12:21928337
|
AAGGGAAG others(110): Show |
A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-2391_285-2275d others(2): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928337 | ||||||
| chr12:21928341
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2278C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928341 | ||||||
| chr12:21928343
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2280T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928343 | ||||||
| chr12:21928344
|
G | GGA | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2282_285-2281i others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928344 | ||||||
| chr12:21928346
|
A | AAAAGAGA others(7): Show |
1 | a0001c0001t0001g0073 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-2297_285-2284d others(16): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928346 | ||||||
| chr12:21928346
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2283T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928346 | ||||||
| chr12:21928430
|
AAAAAG | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2372_285-2368d others(7): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928430 | ||||||
| chr12:21928454
|
G | A | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.285-2391C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928454 | ||||||
| chr12:21928461
|
A | G | 3 | a0001c0001t0001g0053a0002c0007t0001g0039a0002c0007t0001g0049 | 3 | HG02559.hp2 HG02735.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.285-2398T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928461 | ||||||
| chr12:21928471
|
A | G | 3 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0004g0183 | 3 | HG02055.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285-2408T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928471 | ||||||
| chr12:21928660
|
A | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.285-2597T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928660 | ||||||
| chr12:21928802
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.285-2739A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928802 | ||||||
| chr12:21928838
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.285-2775G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928838 | ||||||
| chr12:21928932
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285-2869G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928932 | ||||||
| chr12:21928964
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.285-2901C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928964 | ||||||
| chr12:21928974
|
T | C | 2 | a0002c0007t0001g0039a0002c0007t0001g0049 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.285-2911A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21928974 | ||||||
| chr12:21929031
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.285-2968G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929031 | ||||||
| chr12:21929167
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.285-3104C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929167 | ||||||
| chr12:21929185
|
C | T | 1 | a0001c0002t0023g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.285-3122G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929185 | ||||||
| chr12:21929335
|
G | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02027.hp1 NA18962.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.285-3272C>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929335 | ||||||
| chr12:21929678
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0032others(85): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.285-3615C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929678 | ||||||
| chr12:21929763
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285-3700G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929763 | ||||||
| chr12:21929836
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.285-3773G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929836 | ||||||
| chr12:21929927
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.284+3855C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929927 | ||||||
| chr12:21929982
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.284+3800G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21929982 | ||||||
| chr12:21930418
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+3364C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21930418 | ||||||
| chr12:21930431
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284+3351C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21930431 | ||||||
| chr12:21931365
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284+2417T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21931365 | ||||||
| chr12:21931397
|
T | TA | 6 | a0001c0001t0001g0032a0001c0002t0001g0184a0001c0002t0001g0185others(3): Show | 6 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+2384dupT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21931397 | ||||||
| chr12:21931397
|
TA | T | 9 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(6): Show | 9 | HG02040.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+2384delT | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21931397 | ||||||
| chr12:21931494
|
A | C | 4 | a0001c0001t0001g0069a0001c0001t0005g0067a0001c0001t0011g0068others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+2288T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21931494 | ||||||
| chr12:21932200
|
T | A | 1 | a0001c0004t0001g0119 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.284+1582A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932200 | ||||||
| chr12:21932207
|
CAA | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00408.hp1 HG02027.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.284+1573_284+1574d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932207 | ||||||
| chr12:21932291
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0040others(41): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+1491T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932291 | ||||||
| chr12:21932467
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284+1315G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932467 | ||||||
| chr12:21932575
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284+1207T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932575 | ||||||
| chr12:21932995
|
A | G | 3 | a0001c0001t0001g0053a0001c0002t0012g0002a0001c0003t0009g0209 | 3 | HG02735.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284+787T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21932995 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(328): Show |
1 | a0001c0001t0001g0134 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.284+772_284+773ins others(335): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(323): Show |
1 | a0001c0001t0001g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284+772_284+773ins others(330): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(326): Show |
11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.284+772_284+773ins others(333): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(324): Show |
1 | a0001c0008t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.284+772_284+773ins others(331): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(328): Show |
1 | a0001c0001t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.284+772_284+773ins others(335): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(327): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.284+772_284+773ins others(334): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(329): Show |
1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.284+772_284+773ins others(336): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(328): Show |
5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02074.hp2 HG02300.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+772_284+773ins others(335): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(329): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284+772_284+773ins others(336): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(328): Show |
4 | a0001c0001t0001g0174a0001c0001t0001g0203a0001c0001t0005g0175others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+772_284+773ins others(335): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(327): Show |
50 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.284+772_284+773ins others(334): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(327): Show |
1 | a0001c0004t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.284+772_284+773ins others(334): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933009
|
A | AAAGAAAA others(326): Show |
1 | a0001c0001t0001g0001 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.284+772_284+773ins others(333): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933009 | ||||||
| chr12:21933091
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.284+691C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933091 | ||||||
| chr12:21933196
|
C | A | 1 | a0001c0001t0011g0120 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.284+586G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933196 | ||||||
| chr12:21933228
|
G | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.284+554C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933228 | ||||||
| chr12:21933323
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.284+459C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933323 | ||||||
| chr12:21933392
|
T | C | 3 | a0001c0001t0001g0053a0001c0002t0012g0002a0001c0003t0009g0209 | 3 | HG02735.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284+390A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933392 | ||||||
| chr12:21933655
|
G | A | 1 | a0001c0001t0021g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.284+127C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 4/39 | chr12 | 21933655 | ||||||
| chr12:21933953
|
A | G | 4 | a0001c0006t0001g0191a0001c0006t0005g0192a0002c0007t0001g0039others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-30T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21933953 | ||||||
| chr12:21934004
|
A | C | 2 | a0001c0001t0001g0053a0001c0002t0012g0002 | 2 | HG02735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.143-81T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934004 | ||||||
| chr12:21934042
|
A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.143-119T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934042 | ||||||
| chr12:21934224
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-301A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934224 | ||||||
| chr12:21934344
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.143-421T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934344 | ||||||
| chr12:21934622
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.143-699C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934622 | ||||||
| chr12:21934825
|
A | G | 13 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-902T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934825 | ||||||
| chr12:21934871
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143-948T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21934871 | ||||||
| chr12:21935034
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.143-1111G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21935034 | ||||||
| chr12:21935530
|
A | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0002t0012g0002 | 3 | HG02735.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142+1003T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21935530 | ||||||
| chr12:21935842
|
G | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0190others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+691C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21935842 | ||||||
| chr12:21935938
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.142+595C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21935938 | ||||||
| chr12:21935942
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.142+591T>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21935942 | ||||||
| chr12:21936142
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.142+391A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21936142 | ||||||
| chr12:21936329
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.142+204T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21936329 | ||||||
| chr12:21936414
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.142+119C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21936414 | ||||||
| chr12:21936459
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.142+74T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 3/39 | chr12 | 21936459 | ||||||
| chr12:21936810
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0190others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-116A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21936810 | ||||||
| chr12:21937436
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-20-742T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937436 | ||||||
| chr12:21937528
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(114): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-20-834G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937528 | ||||||
| chr12:21937564
|
A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-20-870T>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937564 | ||||||
| chr12:21937705
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0002t0012g0002 | 3 | HG02735.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-20-1011A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937705 | ||||||
| chr12:21937712
|
T | A | 2 | a0001c0006t0001g0191a0001c0006t0005g0192 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-20-1018A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937712 | ||||||
| chr12:21937846
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-20-1152C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21937846 | ||||||
| chr12:21938027
|
C | G | 1 | a0001c0005t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-20-1333G>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938027 | ||||||
| chr12:21938089
|
C | CAG | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-20-1397_-20-1396d others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938089 | ||||||
| chr12:21938091
|
G | GAA | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0003c0012t0001g0195 | 3 | NA18906.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-1398_-20-1397i others(4): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938091 | ||||||
| chr12:21938166
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20-1472G>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938166 | ||||||
| chr12:21938190
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20-1496C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938190 | ||||||
| chr12:21938287
|
T | C | 1 | a0001c0001t0019g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20-1593A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938287 | ||||||
| chr12:21938384
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0002t0012g0002 | 3 | HG02735.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-20-1690T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938384 | ||||||
| chr12:21938567
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20-1873T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938567 | ||||||
| chr12:21938574
|
T | TTAAA | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-20-1884_-20-1881d others(6): Show |
ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938574 | ||||||
| chr12:21938581
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-20-1887G>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938581 | ||||||
| chr12:21938640
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-1946T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21938640 | ||||||
| chr12:21939320
|
T | C | 9 | a0001c0001t0001g0048a0001c0001t0001g0200a0001c0001t0001g0201others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+1390A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21939320 | ||||||
| chr12:21939514
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02809.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+1196A>G | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21939514 | ||||||
| chr12:21939987
|
A | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-21+723T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21939987 | ||||||
| chr12:21940131
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-21+579T>C | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21940131 | ||||||
| chr12:21940666
|
T | A | 1 | a0001c0003t0009g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-21+44A>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 2/39 | chr12 | 21940666 | ||||||
| chr12:21941108
|
G | T | 1 | a0001c0001t0018g0003 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-137+92C>A | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 1/39 | chr12 | 21941108 | ||||||
| chr12:21941160
|
G | A | 1 | a0001c0001t0006g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-137+40C>T | ABCC9 | ENSG00000069431.14 | transcript | ENST00000261200.9 | protein_coding | 1/39 | chr12 | 21941160 |